Yokukan-san: a review of the evidence for use of this Kampo herbal formula in dementia and psychiatric conditions

Abstract

Japanese traditional herbal medicine (Kampo) has its origins in traditional Chinese medicine (TCM). It was introduced to Japan in the middle of the sixth century and has evolved over the past 1,400 years after combining with Japan’s original folk remedies. While it retains some similarities to TCM, Kampo has evolved in Japan, resulting in a system of medicine that has many differences from TCM. Kampo medicine is considered to be very safe; in Japan, Kampo herbal formulas are manufactured by licensed pharmaceutical companies, prescribed by Western-trained medical doctors (usually as a freeze-dried extract), and have quality control standards similar to those of prescription drugs. The present study examined Yokukan-san (Yi-Gan San in TCM), a Kampo formula that has been used empirically in Japan for more than 400 years. Accumulating clinical trials have demonstrated Yokukan-san’s efficacy in treating patients with behavioral and psychological symptoms of dementia, which has resulted in the Japanese Society of Neurology listing it in the Japanese Guidelines for the Management of Dementia 2010. Efficacy in other diseases and conditions, such as sleep disorders, tardive dyskinesia, aggression, and impulsivity has also been reported. This article reviews both clinical and basic studies of Yokukan-san, with the goal of clarifying its clinical indications.

Keywords:

• Yokukan-san-ka-chimpi-hange
• Japanese traditional medicine
• Asian medicine
• dementia with Lewy bodies (DLB)
• Alzheimer’s disease
• BPSD
• Parkinson’s disease

Introduction

Yokukan-san (YKS; also written as Yokukansan or Yoku-kan-san in Japanese) is a Japanese traditional medicine (Kampo) formula derived from Yi-Gan San in traditional Chinese medicine (TCM). YKS has attracted attention in the field of psychiatry due to reports of its efficacy in patients with dementia.^1–14 In addition, therapeutic effects of YKS have been reported in the treatment of sleep disorders,^15,16 tardive dyskinesia,¹⁷ borderline personality disorder,¹⁸ and schizophrenia-related diseases.^19,20 The claim of YKS’s effectiveness for such a wide variety of indications may produce skepticism toward Kampo medicine and possibly weaken its reputation, especially if YKS is ineffective or harmful because of improper usage. YKS has been approved by the Ministry of Health, Labor, and Welfare in Japan as a covered prescription under the National Health Insurance. This review of YKS provides a general introduction to Kampo medicine, describes the Kampo philosophy, explains the empirical use of YKS based on Kampo diagnosis, and reviews both clinical and basic studies of YKS, with the goal of clarifying the clinical indications of this herbal formula.

Kampo medicine

Overview

Kampo medicine originated in China and has its roots in TCM. It was introduced to Japan in the middle of the sixth century and has evolved over the past 1,400 years.^21,22 While it retains some similarities to TCM, Kampo has evolved independently in Japan, resulting in a system of medicine that has many differences from TCM.^22–24 After its introduction from China, Kampo was combined with Japan’s original folk remedies and was modified by the introduction of formulas and herbs that had not been used in TCM.²⁵ Kampo medicine was the main medical treatment in Japan until Western medicine was introduced from Europe several hundred years ago.^21–24

Kampo herbal formulas in Japan

Although some Kampo herbal formulas are based on classical TCM formulas, the Kampo formulas have been standardized in Japan and use fixed combinations of herbs.^21,22,24 Kampo herbal formulas are regulated in the same manner as pharmaceutical preparations, and are approved and manufactured with standards that are equivalent to those of conventional pharmaceutical medicines. Both manufacturers and the government are involved in extensive monitoring of agricultural and manufacturing processes, as well as in post-marketing surveillance, in order to ensure the quality and safety of these products. The result of this emphasis on standardization is that while a single Kampo herbal formula might be produced by various different manufacturers, it will be subject to the same quality control standards. This high degree of quality and standardization does not necessarily apply if the formula is made outside of Japan.^21,22,24

Kampo is integrated into Japan’s national health care system, and all citizens therefore have access to government-approved Kampo herbal formulas. The Japanese Ministry of Health, Labor, and Welfare has approved 212 Kampo formulas for clinical use, which means that these formulas are also approved for reimbursement under the National Health Insurance program. Of these 212 Kampo formulas, 148 have granule-type (freeze-dried herbal extract) prescriptions and are manufactured by several licensed pharmaceutical companies in Japan. The daily dose is usually in the range of 4.5–27 (most frequently 6–7.5) g of granules, which are generally divided into two or three doses per day. These prescription Kampo formulas are considered to be much easier to take because of the freeze-dried granules, and safer because of the standardization and quality control procedures than decoctions prepared by patients themselves.²² Most physicians in Japan prescribe at least some granule-type Kampo medicines.^21,22,24

Recently, Kampo medicine has received renewed attention because it provides a valid alternative to treating symptoms refractory to conventional medicine. There has also been an emphasis on evaluating Kampo formulas using modern techniques to evaluate their mechanisms of action and to examine their efficacy in the context of Western models of disease and diagnostic criteria.²⁴

Differences between Kampo and conventional Western medicine

Kampo medicine has a diagnostic scheme that is completely different from that of conventional Western medicine. The prescription of a specific formula is usually based on both the patient’s subjective symptoms and objective signs using a Kampo-specific diagnostic examination. This diagnostic approach is discussed in more detail below. Because Kampo prescriptions are usually comprised of multiple herbs, all of which can contain large numbers of active constituents, there is a need to elucidate the clinical effects of these formulas.^21–24

Within Kampo medicine, a single herbal formula prescription is often used to treat a wide variety of symptoms (a practice called “Ibyodochi” in Kampo). One good example of Ibyodochi is YKS, a single prescription that is reported to be effective in treating many different diseases such as dementia,^1–14 sleep disorders,^15,16 tardive dyskinesia,¹⁷ borderline personality disorder,¹⁸ and schizophrenia-related diseases.^19,20 On the other hand, different herbal formulas may also be used to treat the same disease (called “Dobyoichi” in Kampo). For example, in cases of influenza, a Kampo formula called Mao-to (TCM: Ma Huang Tang; English: Ephedra Decoction) might be chosen if the patient has a strong, floating (ie, easily felt), tensed pulse, and shivering followed by a high fever (symptoms suggestive of a vigorous immune response), while a formula called Mao-bushi-saishin-to (TCM: Ma Huang Fu Zi Xi Xin Tang; English: Ephedra, Aconite, and Manchurian Wild Ginger Decoction) might be prescribed if the patient has a low-grade fever together with a weak and sunk pulse (symptoms suggestive of a weak or less vigorous response), even though both sets of symptoms are caused by the same influenza virus.^22,23 Both Ibyodochi and Dobyoichi are often used in the clinical practice of Kampo because Kampo medicine uses a completely different paradigm from conventional diagnostics. The specific prescription is chosen after considering the unique tendencies and reactions to disease of the patient based on Kampo philosophies, which focus on enhancing the body’s resistance to disease by improving self-controlled systems and correcting any physical or mental imbalance.^22,23

Another important distinction is that Kampo does not distinguish between psychiatric and physical symptoms because it regards each human being as a complete and self-controlled unit in which mind and body affect each other. In the Kampo approach, most diseases are considered to be psychosomatic in origin and most herbs are believed to affect both the psyche and the soma equally. Therefore, Kampo treatment is focused on the patient as a whole rather than on the disease. This patient-centered approach allows Kampo to be applied even when the etiology of the condition in question is unknown or when the patient’s symptoms defy easy classification within Western medicine. For these and other reasons, Kampo can be a valid and useful approach to both physical and mental diseases that are refractory to conventional Western medicine.^21–24

Kampo diagnosis

Kampo diagnosis is made based on Kampo-specific philosophies of health and disease, irrespective of conventional Western diagnosis, as mentioned previously. Some of these philosophies derive from TCM, such as the In-Yo (Chinese: Ying-Yang) theory, the Five Phases Theory, and the Six Stages of Disease. Others evolved independently of TCM and are Kampo specific, such as the Ki-ketsu-sui (Qi–Blood–Water) theory, which developed in Japan, is based primarily on abdominal diagnosis, and is a widely used method of choosing herbal formula prescriptions in Japan. This abdominal diagnosis method has the advantages of being a standardized method of examination and of evoking pressure pains on palpation at routine abdominal points that are both objective and reproducible, even among doctors without knowledge of Kampo medicine. Pulse diagnosis can also be used. In TCM, pulse diagnosis tends to be based on the sense impression obtained by each doctor based on his or her training or experience; however, it has been simplified and generalized in Japan, so that even primary care doctors without knowledge of Kampo medicine can utilize this Kampo diagnostic technique.^21–23

Kampo medicine often shows remarkable effectiveness when used in individual cases with the distinctive features that meet the criteria, based on Kampo diagnosis, for choosing a specific Kampo prescription. For example, YKS is appropriate under the following conditions:

• Impatience or frequent anger, irritability, muscular tics or convulsions, and/or blepharospasm.

• According to pulse diagnosis, a tight overall pulse quality, and when the pulse is palpated at three contiguous positions overlying the left and right radial arteries, the relative force of the pulse at the middle position is weak on the left and perhaps also on the right. This pulse pattern indicates liver dysfunction in the Five Phases Theory.

• According to abdominal diagnosis, abdominal tension should not be weak, the rectus abdominis muscle is often strained, and there is often tenderness or discomfort in the hypochondrium on palpation and pulsation at the upper navel region.

Empirical use of YKS

YKS consists of seven herbs (Table 1). This formula dates back to at least 1555, where it was listed in a Chinese medical book “Bao Ying Cuo Yao”. The name of YKS originally meant “medicine suppressing the liver”. The original Chinese description states in “Bao Ying Cuo Yao” that YKS:

Table 1 Components of Yokukan-san

Constituent herbs	Weight (g)
Japanese Angelica root (当帰)	3.0
Atractylodes lancea rhizome (蒼朮)	4.0
Bupleurum root (柴胡)	2.0
Poria sclerotium (茯苓)	4.0
Glycyrrhiza root (甘草)	1.5
Cnidium rhizome (川芎)	3.0
Uncaria hook (釣藤鈎)	3.0

…treats spasm, feverishness, clenching, terrified/simmering mental state, or intolerance to heat and cold caused by pseudo-hyperfunction of the liver and expectoration of sputum, abdominal fullness, loss of appetite, and sleep disorders caused by dysfunction of the spleen, which has a restraining relationship with the liver and is consequently damaged by the liver’s pseudo-hyperfunction.

In the Five Phases Theory, the liver is considered to be the organ that stabilizes mental activities and ameliorates involuntary muscle movements. Thus, the liver often produces anger and/or involuntary muscle movement when its regular function is impaired. However, most Kampo practitioners do not practice based solely on the Five Phases Theory. That is, they do not use all Kampo-specific diagnostics, including detailed pulse diagnosis, and Kampo prescriptions are not chosen based on strict adherence to Kampo-specific philosophy. Instead, YKS is chosen based on subjective symptoms, often in combination with Kampo abdominal diagnosis.

YKS has been used empirically as a treatment for insomnia, irritability, impulsivity, aggression, blepharospasm (abnormal contraction or twitch of the eyelids), tremor or fasciculation of the facial muscles, convulsions, and similar symptoms. It also has a reputation for being effective in the treatment of screaming attacks, sleep terrors, and hypnic myoclonia, especially in infants.^22,23 YKS is considered to have some effects on the excitability of nerves. A famous Kampo medicine doctor, Dotaku Meguro (1739–1798), wrote in his book “San’ei-kan-ryochi-zatsuwa”, “YKS has some efficacy if the patient feels anger”, by which he meant to indicate that YKS could be chosen if this subjective symptom was present and could be expected to exert its efficacy without the need for considering more extensive abdominal and/or tongue diagnosis. Its utility in this specific circumstance might be one of the reasons why YKS can be widely used and still show effectiveness.

Case reports

The first report of the clinical efficacy of YKS appearing in a Western medical journal was a case report in 2005 written by the authors’ group, in which YKS was found to be effective in the treatment of tinnitus, headache, and insomnia in the case of an undifferentiated somatoform disorder.²⁶ This report demonstrated the clinical efficacy of YKS in treating both physical and mental symptoms. Since then, other case reports have also described therapeutic effects of YKS. These are summarized in Table 2.

Table 2 Case reports

Patient (age [years]/sex)	Diagnosis	Symptoms	Daily dose	Results	Adverse effects	Author, year of publication
44/F	Somatoform disorder	Tinnitus, headache, insomnia	7.5 g	Complete remission	None	Okamoto et al, 2005^Citation26
81/M	DLB	Psychosis, sleep disturbance	7.5 g	Markedly improved	None	Shinno et al, 2007^Citation1
60/M 74/F 87/F	REM sleep behavior disorder	Dream-enacting behaviors	2.5–7.5 g	Complete remission	None	Shinno et al, 2008^Citation15
73/F	Charles Bonnet syndrome	Visual hallucinations	7.5 g	Complete remission	None	Miyaoka et al, 2009^Citation28
85/M	Traumatic brain injury	Impulsive and aggressive behaviors	7.5 g	Markedly improved	None	Saito et al, 2010^Citation27
62/F 80/F 75/M	Restless legs syndrome	Unpleasant sensations in the legs	5 g	Complete remission	None	Shinno et al, 2010^Citation16
74/M 78/F	Poststroke emotional incontinence	Uncontrollable episodes of crying or laughing	7.5 g	Complete remission	None	Kajitani and Kanba, 2012^Citation29
50/M	Nocturnal eating/drinking syndrome, restless legs syndrome, schizophrenia	Uncontrollable consumption of food and pain and discomfort in legs at night	2.5 g	Complete remission	None	Kawabe et al, 2012^Citation30
85/M 44/M 29/M	AD Tardive dystonia IED	Aggressive behaviors Muscle contractions Aggressive impulses	5 g 7.5 g 7.5 g	Partially improved (markedly improved after Orengedoku-to augmentation)	None	Okamoto et al, 2013^Citation31

Abbreviations: AD, Alzheimer-type dementia; DLB, dementia with Lewy bodies; F, female; IED, intermittent explosive disorder; M, male; REM, rapid eye movement.

In one of these other case reports, YKS improved psychosis and sleep disturbance in a case of dementia with Lewy bodies (DLB).¹ In a case of an 85-year-old man with dementia that developed after traumatic brain injury, YKS markedly reduced aggressive and impulsive behavior that was refractory to conventional neuroleptics, and did this without producing any adverse effects.²⁷ In non-dementia diseases, YKS has been reported to reduce visual hallucinations due to vision loss in patients with Charles Bonnet syndrome.²⁸ There are also reports on the successful treatment of sleep disorders (three cases of rapid eye movement sleep behavior disorder¹⁵ and three cases of restless leg syndrome),¹⁶ post-stroke emotional incontinence (uncontrollable episodes of crying or laughing in two cases),²⁹ and nocturnal eating/drinking syndrome accompanied by restless leg syndrome and schizophrenia in one case.³⁰ YKS is thus widely used for a variety of diseases in Japan. Furthermore, the authors’ group recently reported that the addition of Orengedoku-to, another Kampo formula, to YKS was markedly effective in three cases (Alzheimer-type dementia, tardive dystonia, and intermittent explosive disorder) and that this augmentation with Orengedoku-to is worth trying in case in which the efficacy of YKS is limited.³¹

In these cases, YKS has been reported to be effective in the treatment of not only mental but also physical symptoms such as tinnitus, headache, and restless leg syndrome, which is consistent with the notion that Kampo medicine is useful for harmonizing mind and body.

Controlled human studies

Studies on dementia

Although there have been many controlled studies, to the best of the authors’ knowledge, there have been no placebo-controlled studies of YKS. Part of the reason for this is that, due to the unique flavor and odor of YKS, it is difficult to prepare a suitable placebo. The first controlled study of YKS (a randomized, observer-blind, multicenter, controlled trial) was performed in early 2005.² In that study, 4 weeks of treatment with YKS significantly improved scores on both the Neuropsychiatric Inventory (NPI) for the assessment of behavioral and psychological symptoms of dementia (BPSD) and the Barthel Index for activities of daily living (ADL) in 52 patients with mild to severe dementia. In this study, Mini-Mental State Examination results were unchanged. Also of note, extrapyramidal symptoms were not observed with YKS, demonstrating that YKS has a different therapeutic mechanism from that of antipsychotic agents that improve BPSD and ADL without impairing cognitive function or causing extrapyramidal symptoms. This report marked the beginning of the research interest in YKS for the treatment of dementia. Since that time, there have been many other controlled studies on YKS (Table 3). The same group that conducted the original controlled trial in dementia subsequently reported the efficacy of YKS in treating cholinesterase inhibitor-resistant visual hallucinations and neuropsychiatric symptoms of DLB.³ Since that time (late 2005), YKS has become the second-line treatment for DLB in Japan. The efficacy of YKS in DLB was further validated in a larger population (54 patients) by the same group in 2012.¹¹

Table 3 Controlled studies of dementia

Design	Diagnosis	Study size	Dose, duration	Results	Adverse effects	Author, year of publication
Prospective, randomized, observer-blind, multicenter, open-label	Mild-to-severe dementia	N=52 (YKS group n=27; control n=25)	7.5 g/day, 4 wks	Significant improvement in NPI and BI scores. No significant change in MMSE	EPS were not observed. Two participants became oversedated after trial (well tolerated with 3–4.5 g/day of YKS)	Iwasaki et al, 2005^Citation2
Prospective, single-arm, open-label	Mild-to-severe DLB	N=14	7.5 g/day, 4 wks	Significant improvement in NPI and BI scores. No significant change in MMSE. Visual hallucinations disappeared within 2 weeks in 12 of 15 patients	One dropout due to drowsiness	Iwasaki et al, 2005^Citation3
Prospective, single-arm, open-label	Mild-to-severe dementia	N=5 (DLB n=3; AD n=2)	7.5 g/day, 4 wks	Significant improvement in total sleep time, number of awakenings, PLMs index in PSG as well as NPI scores. Significant increase of Stage II sleep. No significant change in MMSE	None	Shinno et al, 2008^Citation4
Prospective, randomized, cross-over, multicenter, open-label	Mild-to-severe AD (including mixed-type dementia), DLB	N=103 (YKS administration for first 4 wks and non-treatment for next 4 wks n=53; non-treatment for first 4 wks and YKS administration for next 4 wks n=50)	7.5 g/day, 4 wks	NPI scores significantly improved in first 4 wks in both groups and also markedly improved in the YKS treatment period in both groups. No significant change in MMSE, BI, or IADL	Gastrointestinal symptoms (vomiting/diarrhea, nausea, epigastric distress) in three patients, hypokalemia in two patients (3.8→3.4, 4.1→2.2 mEq/L) and one of two also showed sedation, leg edema in one patient	Mizukami et al, 2009^Citation5
Prospective, randomized, open-label	Mild-to-severe AD	N=15 (YKS group n=10; control n=5)	7.5 g/day, 12 wks	Decrease of the sulpiride dose (continuation therapy for BPSD), significant improvement in NPI, unchanged MMSE scores	Hypokalemia in two patients (one of them was supplemented with potassium until the end of the study)	Monji et al, 2009^Citation6
Prospective, single-arm, multicenter, open-label	Mild-to-severe AD (including mixed-type dementia)	N=26	7.5 g/day, 4 wks	Significant improvement in NPI scores. No significant change in MMSE or DAD	Hypokalemia in one patient and oversedation in one patient	Hayashi et al, 2010^Citation7
Prospective, randomized, multicenter, open-label	Mild-to-severe AD (including mixed-type dementia)	N=63 (YKS group n=30; control n=33)	7.5 g/day, 4 wks	Significant improvement in NPI scores. No significant change in MMSE, DAD, ZBI, or SDS	None	Okahara et al, 2010^Citation8
Prospective, single-arm, open-label	Parkinsonian dementia	N=14 (PDD n=7; PD n=7)	7.5 g/day, 4 wks	Significant improvement in NPI scores after 1–2 weeks of YKS administration. Recurrences of hallucinations in five PD and three PDD patients after cessation of YKS treatment (no recurrence in the remaining patients during the 4-week follow-up period)	Sialorrhea in one PDD patient and mild elevation of blood liver enzymes in one PD patient	Kawanabe et al, 2010^Citation9
Prospective, single-arm, open-label	Mild-to-severe FTD	N=20	7.5 g/day, 4 wks	Significant improvement in NPI and SRI scores	Hypokalemia in two patients	Kimura et al, 2010^Citation10
Prospective, single-arm, multicenter, open-label	Mild-to-severe DLB	N=54	7.5 g/day, 4 wks	Significant improvement in NPI and ZBI scores. No significant change in MMSE or DAD	Hypokalemia in four patients and worsening hypotension in one patient. Three patients discontinued YKS due to spasticity and exacerbation of BPSD, edema, and nausea	Iwasaki et al, 2012^Citation11
Prospective, single-arm, open-label	Mild-to-severe VaD	N=13	7.5 g/day, 4 wks	Significant improvement in NPI scores. No significant change in MMSE, BI, DAD, or UPDRS	None	Nagata et al, 2012^Citation12
Prospective, single-arm, open-label	CRF patients with mild-to-severe dementia receiving hemodialysis three times per week	N=11 (AD n=8; VaD n=3)	7.5 g/day, 4 wks	Significant improvement in NPI. No significant change in BI. Blood potassium remained within the normal range during YKS administration although 6.5%–41.2% of CRF patients receiving hemodialysis were supposed to be hyperkalemic	Mild and transient (nausea in one patient and tiredness in one patient)	Sumiyoshi et al, 2013^Citation13
Prospective, randomized, rater-blinded, flexible-dosed, triple group trial	Mild-to-severe dementia (dementia subtypes were diagnosed into AD, VaD, or DLB)	N=76 (YKS n=26; risperidone n=25; fluvoxamine n=25; patients were randomized to a flexible oral dosing regimen of either YKS, risperidone, or fluvoxamine by the trial investigator to preserve rater blinding)	YKS (2.5–7.5 g/day), risperidone (0.5–2.0 mg/day), or fluvoxamine (25–200 mg/day), 8 wks	NPI scores were improved in all 3 drug groups with no significant between-group differences. No significant change in MMSE or FIM. DIEPSS scores did not change in the YKS and fluvoxamine groups, but increased significantly in the risperidone group	No severe side effect possibly related to YKS. Constipation and muscle rigidity were significantly increased in the risperidone group compared with the YKS and fluvoxamine groups	Teranishi et al, 2013^Citation14

Abbreviations: AD, Alzheimer-type dementia; BI, Barthel Index; CRF, chronic renal failure; DAD, Disability Assessment for Dementia; DIEPSS, Drug-Induced Extrapyramidal Symptoms Scale; DLB, dementia with Lewy bodies; EPS, extrapyramidal symptoms; FIM, Functional Independence Measure; FTD, frontotemporal dementia; IADL, instrumental activities of daily living; MMSE, Mini-Mental State Examination; NPI, Neuropsychiatric Inventory; PD, Parkinson’s disease; PDD, Parkinson’s disease with dementia; PLMs, periodic limb movement during sleep; PSG, polysomnography; SDS, Self-rating Depression Scale; SRI, Stereotypy Rating Inventory; UPDRS, Unified Parkinson’s Disease Rating Scale; VaD, vascular dementia; wks, weeks; YKS, Yokukan-san; ZBI, Zarit Burden interview.

In 2009, a randomized crossover study involving 103 dementia patients was carried out and further supported the clinical efficacy of YKS in patients with BPSD.⁵ Another report found that 4 weeks of YKS administration significantly increased total sleep time, sleep efficiency, and stage II sleep, and decreased the numbers of arousals and periodic limb movements as well as ameliorating psychiatric symptoms in BPSD.⁴ This suggests that part of the efficacy of YKS in such cases might be secondary to its effects on sleep.

Three open-label studies have also supported the effectiveness of YKS in people with BPSD and Alzheimer-type dementia.^6–8 YKS treatment for 4 weeks has been reported to be effective for treating BPSD in patients with Parkinson’s disease and those with Parkinson’s disease with dementia. Significant improvements in behavioral and psychological symptoms, particularly in the incidence and duration of hallucinations, were observed in most Parkinson’s disease and Parkinson’s disease with dementia patients; however, no significant changes were observed in laboratory test results, cognitive function, ADL, or parkinsonism.⁹ Four weeks of YKS treatment significantly improved NPI scores and the Stereotypy Rating Inventory in 20 patients with frontotemporal dementia¹⁰ and NPI scores in 13 patients with vascular dementia,¹² suggesting that YKS alleviates the behavioral symptoms of frontotemporal and vascular dementia as well as other types of dementia.

YKS has also been found to exert significant therapeutic effects without severe adverse effects on the behavioral symptoms of dementia among chronic renal failure patients receiving hemodialysis three times per week.¹³ To the best of the authors’ knowledge, the most recent controlled clinical trial was carried out in 2013 in a well-structured study, in which patients were randomized by the trial investigator to preserve rater blinding to a flexible oral dosing regimen of either YKS, risperidone, or fluvoxamine, and demonstrated that YKS improved NPI scores without causing extrapyramidal symptoms and with no significant between-group differences.¹⁴

There is only one systematic review of YKS’s effectiveness on dementia among four studies^2,5,6,8 published in 2013.³² The meta-analysis in this review concluded that YKS was superior to usual care (control) in the reduction of total NPI scores (P=0.0009) and ADL scores (P=0.04), and more efficacious especially in reducing scores on some NPI subscales (delusions, hallucinations, and agitation/aggression) than usual care (P<0.00001–0.0009).

Controlled studies on other diseases

YKS’s therapeutic effects on diseases other than dementia have also been reported since 2008 (Table 4). An open-label study reported the efficacy of YKS on visual hallucinations due to vision loss in patients with Charles Bonnet syndrome in 2011.³³ Three reports have suggested the potential for use in persons with schizophrenia-related diseases.^17,19,20 Four weeks of adjunctive therapy with YKS for treatment-resistant schizophrenia has been found to decrease Positive and Negative Syndrome Scale scores on the schizophrenia subscale without changing Drug-Induced Extrapyramidal Symptom Scale total scores.¹⁹ Similarly, 4 weeks of adjunctive therapy with YKS for very late-onset schizophrenia-like psychosis significantly improved Positive and Negative Syndrome Scale, Brief Psychiatric Rating Scale, and Clinical Global Impressions scores without impairing cognitive function or aggravating extrapyramidal symptoms.²⁰ Twenty-two patients with schizophrenia who had neuroleptic-induced tardive dyskinesia were given YKS for 12 weeks in an open-label study.¹⁷ Intriguingly, there was a statistically significant improvement in both tardive dyskinesia and psychotic symptoms. These three studies suggest that YKS may be a safe adjunctive therapy in persons with refractory schizophrenia or schizophrenia-like psychosis with vulnerability to extrapyramidal adverse effects.

Table 4 Controlled studies on other diseases

Design	Diagnosis	Study size	Dose, duration	Results	Adverse effects	Author, year of publication
Prospective, single-arm, open-label	Schizophrenia and neuroleptic-induced tardive dyskinesia	N=22	7.5 g/day, 12 wks	Significant improvement in AIMS, both positive and negative symptoms in PANSS, and CGI scores	Mild and transient (nausea in one patient and constipation in one patient)	Miyaoka et al, 2008^Citation17
Prospective, single-arm, open-label	Borderline personality disorder	N=20	2.5–7.5 g/day, 12 wks	Highly significant improvement in BPRS, HAM-D, AQ, GAF, and CGI scores	Mild and transient (headache and nausea in two patients and tiredness in one patient)	Miyaoka et al, 2008^Citation18
Prospective, randomized, open-label	Treatment-resistant schizophrenia	YKS group (N=34) versus control (N=25)	2.5–7.5 g/day, 4 wks	Significant improvement in both positive and negative symptoms in PANSS scores. No significant change in DIEPSS	Mild and transient (nausea in two patients and tiredness in one patient)	Miyaoka et al, 2009^Citation19
Prospective, cross-over, open-label	Huntington’s disease	N=4 (two patients took YKS for 8 wks first, and after 4 wks of washing out, they took SRBT for 8 wks. Two other patients took those medicines in reverse order)	Doses not shown, 8 wks	Significant improvement in UHDRS-m scores by not SRBT but YKS treatment without extrapyramidal symptoms or changes of cognition or ADL scores	None	Satoh et al, 2009^Citation36
Prospective, single-arm, open-label	Charles Bonnet syndrome	N=20	2.5–7.5 g/day, 4 wks	Significant improvement in NPI, hallucination subscale of the PANSS, and CGI scores	Mild and transient (nausea in three patients)	Miyaoka et al, 2011^Citation33
Prospective, single-arm, open-label	Pervasive developmental disorder not otherwise specified (PDD-NOS) or Asperger disorder	N=40	2.5–7.5 g/day, 12 wks	Significant improvement in CGI and ABC-I scores	Mild and transient (nausea in five patients)	Miyaoka et al, 2012^Citation34
Prospective, single-arm, open-label	Very late-onset schizophrenia-like psychosis	N=40	2.5–7.5 g/day, 4 wks	Significant improvement in both positive and negative symptoms, general psychopathology, and total scores in PANSS. No significant change in MMSE, Simpson–Angus score, Barnes Akathisia Scale index, or AIMS	None	Miyaoka et al, 2013^Citation20
Prospective, single-arm, open-label	Pervasive developmental disorder in children and adolescents (6–17 years old)	N=20	2.5–7.5 g/day, 12 wks	Significant improvement in CGI, CGAS, and ABC-I scores	Mild and transient (drowsiness in two patients)	Wake et al, 2013^Citation35

Abbreviations: ABC-I, Aberrant Behavior Checklist-Irritability subscale; ADL, activities of daily living; AIMS, Abnormal Involuntary Movement Scale; AQ, Aggression Questionnaire; BPRS, Brief Psychiatric Rating Scale; CGAS, Children’s Global Assessment Score; CGI, Clinical Global Impression; DIEPSS, Drug-Induced Extrapyramidal Symptom Scale; GAF, Global Assessment of Functioning; HAM-D, Hamilton Rating Scales for Depression; MMSE, Mini-Mental State Examination; NPI, Neuropsychiatric Inventory; PANSS, Positive and Negative Syndrome Scale; SRBT, Saiko-ka-ryukotsu-borei-to; UHDRS-m, Unified Huntington’s Disease Rating Scale-motor assessment; wks, weeks; YKS, Yokukan-san.

One study suggests benefits in patients with borderline personality disorder.¹⁸ Twenty female outpatients diagnosed with this psychiatric condition completed a 12-week open-label study with YKS. There was a statistically significant reduction on both self-rated and clinician-rated scales for low mood, impulsivity, and aggression. Furthermore, two studies reported that YKS improved Aberrant Behavior Checklist-Irritability subscale and Clinical Global Impressions scores in subjects with pervasive developmental disorders and Asperger disorder.^34,35

Benefits for neurological symptoms in neurodegenerative disease have also been reported. As mentioned earlier, within Kampo medicine, involuntary movements are one of the criteria for considering YKS. Four Huntington’s disease patients showed a significant decrease in their Unified Huntington’s Disease Rating Scale-motor assessment scores following 8 weeks of YKS treatment; in this study there were no extrapyramidal symptoms or changes in cognition or ADL.³⁶

In summary, various controlled studies have demonstrated the effectiveness of YKS not only on emotion-specific symptoms and psychotic symptoms but also on neurological symptoms. This is consistent with published case reports showing its effectiveness in individuals with both mental and physical symptoms, and with the traditional use of this Kampo formula.

Animal studies

A variety of animal studies have been done to support the clinical efficacy of YKS and elucidate its therapeutic mechanisms, which are summarized in Table 5.

Table 5 Animal studies

Antidepressant-like effects

YKS increased the number of wheel rotations in a water tank, counted as escape attempts, at lower doses (60 and 150 mg/kg/day) and decreased the number at the highest dose (300 mg/kg/day)^Citation37

Pain-relieving effects

• YKS reduced the number of acetic acid-induced writhing responses^Citation37

• YKS inhibited mechanical and cold allodynia in the von Frey hair or acetone test, respectively^Citation38

Anti-aggressive properties

YKS ameliorated aggressiveness induced by:

• Social isolation^Citation39

• Zinc deficiency^Citation40

• Social isolation in zinc-deficient and pair-fed mice^Citation41

• The intravenous injection of para-Chloroamphetamine^Citation42

• Intracerebroventricular injection of amyloid beta protein^Citation43

Anxiolytic effects

• Repeated administration of YKS decreased anxiety-like behavior in an open-field test and an elevated plus-maze test in a dose-dependent manner^Citation45

• YKS’s anxiolytic effect was inhibited by flumazenil, a benzodiazepine receptor antagonist^Citation46

• Three months of YKS administration improved age-related anxiety in F344/N aged rats^Citation47

• Repeated administration of YKS suppressed rats’ freezing behavior on re-exposure to the box where they had experienced footshock in a contextual fear conditioning test and increased the time spent in open arms in rats subjected to footshock stress compared to control rats^Citation48

Efficacy of YKS in dementia models of Alzheimer’s disease

• Treatment with YKS for 2 months reduced the increased number of entries and the time spent in open arms in the elevated plus-maze test, treatment for 5 months shortened the time until reaching the platform in the Morris water maze test, and treatment for 9 months suppressed the increase in locomotion in the open-field test in the Tg2576 mice expressing the human form of the APP695SWE^Citation49

• YKS ameliorated spatial memory impairment in an early-phase Alzheimer’s disease rat model^Citation51

• YKS improved learning and memory impairments in olfactory bulbectomized mice^Citation52

Studies using animal models of other dementia types

YKS ameliorated:

• Memory disturbance as well as BPSD-like behavior such as anxiety-like behavior, increases in aggressive behaviors, and decreases in social behaviors in thiamine-deficient rats^Citation53

• Age-related impairments of working memory and reversal learning in aged (24-month-old) rats^Citation55

• Anxiety-like behaviors in rats subjected to repeated cerebral ischemia^Citation56

Studies on other clinical efficacies of YKS

• YKS ameliorated vacuous chewing movement in rats, an index for tardive dyskinesia, caused by haloperidol decanoate^Citation57

• YKS had a reversal effect on the decrease in pentobarbital sleep by social isolation without affecting pentobarbital sleep in group-housed mice^Citation58

Abbreviations: BPSD, behavioral and psychological symptoms of dementia; YKS, Yokukan-san.

Antidepressant-like and pain-relieving effects

To test the antidepressant-like and pain-relieving effects of YKS, a study was designed to assess behavioral and mood effects under circumstances intended to cause behavioral despair.³⁷ YKS was administered for 14 consecutive days in the drinking water of mice. The mice were then placed for 15 minutes in a water tank from which there was no escape containing a water wheel. In this model, the number of wheel rotations counted as escape attempts. YKS administration had a biphasic effect, markedly increasing the number of wheel rotations at lower doses (60 and 150 mg/kg/day) but decreasing the number at the highest dose (300 mg/kg/day). This study suggests the possibility that YKS has antidepressant-like effects at some doses and counterproductive effects at other doses. In the same paper, YKS was reported to reduce the number of acetic acid-induced writhing responses and have an antinociceptive function.

YKS is sometimes effective in clinical practice for ameliorating neuropathic pain symptoms and another paper reports on YKS’s pain-relieving effect, validating such clinical efficacy in a rat chronic constriction injury model.³⁸ YKS significantly inhibited mechanical and cold allodynia in the von Frey hair or acetone test, respectively, while amitriptyline, a tricyclic antidepressant, demonstrated moderate, but not significant, antiallodynic effects in the same tests. YKS significantly inhibited the cerebrospinal fluid dialysate level of glutamate, which had been increased by stimulation with a brush or acetone, and the glutamate transporter inhibitors DL-threo-β-hydroxyaspartate and dihydrokainate decreased YKS-induced antiallodynic actions in chronic constriction injury rats, suggesting that the antiallodynic effects of YKS are related to glutamatergic neurotransmission via the activation of glutamate transporters.

Anti-aggressive properties

Animal studies have also revealed anti-aggressive properties of YKS. This is consistent with both traditional uses and results from human studies. YKS has been found to ameliorate aggressiveness induced by social isolation in rats,³⁹ by zinc deficiency in young mice,⁴⁰ by social isolation in zinc-deficient and pair-fed mice,⁴¹ by the intravenous injection of para-chloroamphetamine in rats,⁴² and by the intracerebroventricular injection of amyloid β protein in mice, which is a model for Alzheimer’s disease.⁴³ Additionally, YKS (300 mg/kg) inhibited methamphetamine-induced hyperlocomotion, while YKS at the same dose had no effect on hyperlocomotion induced by MK-801, an N-methyl-D-aspartate receptor antagonist, suggesting that the psychopharmacologic effects of YKS might be mediated by inhibiting the activity of the dopaminergic system.³⁹ Another paper discusses the possibility that the anti-aggressive effect of YKS may be related to the glutamatergic system.⁴¹ Both MK-801 and aminooxyacetic acid, a γ-amino butyric acid (GABA) transaminase blocker, attenuated aggressive behavior in zinc-deficient mice but not in pair-fed mice, while YKS (312 mg/kg/day) attenuated aggressive behavior in both groups of mice, suggesting that YKS ameliorates the social isolation-induced aggressive behavior of zinc-deficient and pair-fed mice through action against the glutamatergic neurotransmitter system and other neurotransmitter systems. YKS’s ameliorating effect on the isolation-induced aggressive behavior of zinc-deficient mice is probably related to amelioration of abnormal glucocorticoid secretion.⁴⁰ This is because the basal level of serum glucocorticoid, which was significantly higher in zinc-deficient mice, was decreased by YKS administration, because YKS administration to zinc-deficient mice significantly increased serum glucocorticoid levels after a resident-intruder test, and because after the test the significant difference in serum corticosterone levels between control and zinc-deficient mice disappeared.⁴⁰

There are several reports that indicate that the anti-aggressive efficacy of YKS is related to the serotonergic system. In one such study, para-chloroamphetamine reduced not only the 5-hydroxytryptamine (5-HT) concentration but also the high potassium-induced 5-HT release in the rat hypothalamus.⁴² In the same study, a single injection of YKS ameliorated the para-chloroamphetamine-induced decrease in social behavior but not aggressive behavior. Additionally, chronic treatment for 14 days with YKS ameliorated para-chloroamphetamine-induced abnormal behavior, decreased social behavior, and increased aggressive behavior. The ameliorative effects of chronic YKS on behavior were counteracted by the co-administration of WAY-100635, a 5-HT_1A antagonist. These results suggest that YKS may have two different effects: an acute effect on social behavior and a chronic effect on aggressive behavior. One of the mechanisms of these effects of YKS may be related to its agonistic effect on 5-HT_1A receptors.

Another study suggests that geissoschizine methyl ether in Uncaria hook, a constituent herb of YKS, is a potent 5-HT_1A receptor agonist and a candidate for explaining the pharmacological effect of YKS on aggressiveness and sociality in socially isolated mice.⁴⁴

Anxiolytic effects

Several animal studies have shown anxiolytic effects of YKS. While neither single nor repeated administration of YKS had an effect on basal or stress-induced levels of serum corticosterone, repeated administration of YKS decreased anxiety-like behavior in an open-field test and an elevated plus-maze test in a dose-dependent manner in mice, though a single administration had no effect on locomotor activity or anxiety-like behavior.⁴⁵ In addition, repeated administration of YKS also decreased stress-induced c-Fos expression in the prelimbic cortex and basolateral and medial amygdaloid nuclei.⁴⁵ These results suggest that not single, but repeated, administration of YKS yields anxiolytic effects without affecting serum corticosterone levels, and that its anxiolytic effect may be associated with attenuated neuronal activity in the medial prefrontal cortex and amygdala.

In another study on mice, the anxiolytic effect of YKS was inhibited by pretreatment with the benzodiazepine receptor antagonist flumazenil, suggesting that YKS produces an anxiolytic effect mediated by the benzodiazepine system.⁴⁶ Three months of YKS administration improved aspects of age-related anxiety in F344/N aged rats in a study whose results suggest that this improvement may result from the enhancement of serotonergic and dopaminergic transmissions.⁴⁷

Another rodent behavioral study indicates that the anxiolytic effect of YKS is related to the serotonergic system.⁴⁸ Repeated administration of YKS did not affect the decrease in locomotor activity induced by re-exposure to the footshock box 14 days after footshock stress in an open-field test. In a contextual fear conditioning test, rats that had experienced footshock showed significant freezing behavior on re-exposure to the box 14 days after footshock stress, but YKS significantly suppressed this behavior. In an elevated plus-maze test on the 16th day after the contextual fear conditioning test, YKS significantly increased the time spent in open arms in rats subjected to footshock stress compared to control rats. Interestingly, these anxiolytic effects by YKS were antagonized by WAY-100635, the aforementioned selective 5-HT_1A receptor antagonist, in the contextual fear conditioning test but not in the elevated plus-maze test. Furthermore, the 5-HT_1A receptor agonist buspirone significantly suppressed freezing behavior in the contextual fear conditioning test but induced no change in the time spent in open arms in the elevated plus-maze test.⁴⁸ These findings strongly suggest that YKS has an ameliorating effect on anxiety-like behaviors induced by both innate fear and memory-dependent fear, and that YKS’s anxiolytic effect on memory-dependent fear induced by aversive stress is exerted via 5-HT_1A receptors.

Efficacy of YKS in dementia models of Alzheimer’s disease

The effects of YKS on dementia have been investigated in rodent models. Three behavioral tests revealed that YKS improves learning and non-cognitive disturbance in Tg2576 mice expressing the human form of APP695SWE (APP-Tg mice), which is considered to be an animal model of Alzheimer’s disease. In one study using APP-Tg-positive mice, treatment with YKS for 2 months significantly reduced the increased number of entries and the time spent in open arms in the elevated plus-maze test, treatment for 5 months shortened the time until reaching the platform in the Morris water maze test, and treatment for 9 months significantly suppressed the increase in locomotion in the open-field test.⁴⁹ These results suggest that YKS ameliorates learning deficits and non-cognitive defects including a decrease in anxiety (or disinhibition) and an increase in locomotor activity (hyperactivity) in APP-Tg-positive mice. In another study, the same group reports that YKS inhibited amyloid β protein aggregation in a concentration-dependent manner in vitro and that YKS prevented the accumulation of cerebral amyloid β protein in vivo using APP-Tg-positive mice, supporting YKS’s efficacy in preventing and/or treating Alzheimer’s disease.⁵⁰ Additionally, a recent study revealed that YKS has an ameliorative effect on spatial memory impairment in an early-phase Alzheimer’s disease rat model, and that its therapeutic mechanism is mediated by an increase in acetylcholine release and the modulation of DMN1 expression, leading to improved synaptic function.⁵¹ The ameliorative effects of YKS on learning and memory impairments were also studied using olfactory bulbectomized mice, another animal model of Alzheimer’s disease.⁵² Olfactory bulbectomized mice caused spatial working memory and non-spatial working memory impairments that were reversed by YKS and also by donepezil. In addition, YKS treatment reversed olfactory bulbectomized mice-induced downregulation of choline acetyltransferase and muscarinic M₁ receptor expression without affecting muscarinic M₃ receptor expression or acetylcholinesterase activity. These results demonstrate that YKS has a therapeutic effect not only on BPSD but also on the memory impairment of Alzheimer’s disease that is partly mediated by muscarinic receptor stimulation and the normalization of central cholinergic systems.

Studies using animal models of other dementia types

There have been several reports using rodent models of dementia other than Alzheimer’s disease. Thiamine-deficient (TD) rats, a rodent dementia model, develop degeneration of cerebral cells and dementia-like symptoms, including memory disturbance and behavioral and psychological symptoms. YKS has been found to ameliorate this memory disturbance as well as BPSD-like behavior such as anxiety-like behavior, increases in aggressive behaviors, and decreases in social behaviors in TD rats in a dose-dependent manner.⁵³ In addition, the same group showed that YKS ameliorates not only TD-induced aggressive behavior and neurological symptoms but also degeneration of the cerebral cells, which provides further support for YKS’s efficacy using electron microscopic evidence.⁵⁴ In another study, the ameliorative effect of YKS on age-related impairments of working memory and reversal learning was examined in aged rats.⁵⁵ The ability to learn initially a reward rule for a T-maze discrimination task (initial learning) was tested in young control (4-month-old), aged control (24-month-old), and YKS-treated aged (24-month-old) rats. Working memory and reversal learning were also examined in delayed alternation and reversal discrimination T-maze tasks, respectively. YKS treatment significantly reversed age-related decreases in accuracy in the delayed alternation and reversal discrimination tasks. These ameliorative effects of YKS on impaired delayed alternation performance were reduced by intracranial infusions of a dopamine D1 receptor antagonist, SCH 23390, into the prelimbic cortical region of the prefrontal cortex, suggesting that YKS’s ameliorative effect on age-related impairments of working memory and reversal learning may be mediated by a dopaminergic mechanism in the prefrontal cortex.⁵⁵

There has also been a report on the therapeutic effect of YKS in a rodent model of cerebrovascular dementia.⁵⁶ Rats subjected to repeated cerebral ischemia exhibited anxiety-like behavior in a plus-maze task, a light/dark box test, and an open-field task. Those anxiety-like behaviors were reversed by YKS administration, suggesting that YKS improves BPSD in patients with cerebrovascular dementia as well as other types of dementia.

Animal studies on other clinical efficacies of YKS

There have been other intriguing animal behavioral studies supporting YKS’s other clinical efficacies. YKS has been found to ameliorate vacuous chewing movement in rats, an index for tardive dyskinesia, caused by haloperidol decanoate.⁵⁷ This effect of YKS may be involved in extracellular glutamate level and GLT1(glutamate transporter 1) messenger RNA expression in the striatum. YKS has a reversal effect on the decrease in pentobarbital sleep by social isolation without affecting pentobarbital sleep in group-housed mice.⁵⁸ This prolongation of sleeping time in socially isolated mice is reversed by bicuculline, a competitive antagonist of GABA_A receptors, and flumazenil, a benzodiazepine receptor antagonist, but not WAY100635, a 5-HT_1A receptor antagonist. These results suggest that the GABA_A–benzodiazepine receptor complex, but not 5-HT_1A receptors, is involved in YKS’s ameliorating effect on sleep.

Potential mechanisms of action of YKS

The study using the TD rat model revealed that YKS inhibited the degeneration of neuronal and astroglial cells in the brain stem, hippocampus, and cortex.⁵³ It also produced a rise in extracellular glutamate in the ventral posterior medial thalamus, suggesting that YKS might inhibit glutamate-mediated excitotoxicity. In a separate study by the same research group, YKS was reported to exert neuroprotective effects, protecting against the degeneration of cerebral cells in TD rats.⁵⁴ Neuroprotective effects have also been reported for β amyloid-induced cytotoxicity in rat cortical neurons,⁵⁹ glutamate cytotoxicity due to oxidative stress in PC12 cells,⁶⁰ and glutamate-mediated excitotoxicity in cultured cells⁶¹ and primary cultured rat cortical neurons.⁶² YKS has also been reported to have suppressive effects on excessive glutamate release in zinc-deficient rats.^63,64 These rodent studies strongly suggest that the glutamatergic neurotransmitter system may play an important role in the mechanism by which YKS exerts a neuroprotective effect.

Another key to YKS’s psychopharmacological effects may be the serotonin (5-HT) system. Repeated, but not acute, treatment with YKS (300 mg/kg/day for 14 days per os) significantly decreased the expression of 5-HT_2A receptors (a receptor subtype in the 5-HT system) in the prefrontal cortex and inhibited the head-twitch response in mice induced by 2, 5-dimethoxy-4-iodoamphetamine (a 5-HT_2A receptor agonist).⁶⁵ As described previously, YKS’s anxiolytic effect on memory-dependent fear is exerted via 5-HT_1A receptors.⁴⁸ YKS was also found to inhibit the binding of (³H)8-OH-DPAT (a research chemical used to study the function of the 5-HT_1A receptor) to 5-HT_1A receptors in a concentration-dependent manner.⁶⁶ In another study, the ameliorative effects of YKS on aggressive behavior were counteracted by the co-administration of a 5-HT_1A antagonist,⁴² suggesting that YKS has an agonistic effect on 5-HT_1A receptors. Given reports that YKS improves abnormalities of the 5-HT system, such as the function of 5-HT_2A receptors associated with BPSD in Alzheimer’s disease⁶⁷ and reports that tandospirone (a 5-HT_1A partial agonist) improves BPSD symptoms,⁶⁸ the effects of YKS on the serotonin system might play an important role in its clinical effects.

There are several reports on other possible therapeutic mechanisms of YKS. Endoplasmic reticulum stress is known to play an important role in the pathogenesis of Alzheimer’s disease, particularly in neuronal death. In one study, YKS inhibited endoplasmic reticulum stress-induced neuronal death in cultured cells by regulating the unfolded protein response.⁶⁹ Another report discusses the effect of YKS on cell signaling pathways.⁷⁰ YKS showed neuroprotective effects in vitro and in vivo and rescued dopaminergic neurons from 1-methyl-4-phenylpyridine/1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine toxicity via the PI3K/Akt pathway.

Adverse effects

The adverse effects of YKS in the human case reports and controlled studies are summarized in Tables 2–4. The most frequently reported side effect is hypokalemia resulting from pseudoaldosteronism, presumably caused by Glycyrrhiza (licorice) root, one of the components of YKS. Potassium supplementation was needed during YKS administration in one case,⁶ and potassium levels quickly returned to baseline levels after patients stopped taking YKS in all cases. Hypokalemia was observed only in trials for dementia,^5–7,10,11 which might imply that YKS has a greater tendency to cause hypokalemia among the elderly than among the non-elderly.

YKS infrequently evoked tiredness¹³ and oversedation (or drowsiness)^2,3,5,7,35 among the elderly and children and adolescents, and more infrequently caused tiredness in other generations.^18,19

Gastrointestinal complaints have been reported in the elderly^5,11,13 and the non-elderly;^{17–19,33,34} however, these complaints are mild and transient. Mild elevation of blood liver enzymes was observed in one case.⁹

There is a concern that YKS might cause interstitial pneumonitis. While this is a very rare adverse effect to Kampo medicines, the potential for interstitial pneumonitis is considered to exist with any Kampo formula. One conference presentation given in Japan and published in abstract form only reported interstitial pneumonitis possibly caused by YKS,⁷¹ but to the best of the authors’ knowledge, there has been no detailed report published to date.

Herbal formulae containing Angelica root or Bupleurum root have been reported to cause hepatotoxic responses in some patients⁷² and YKS should be also monitored for hepatotoxicity and dermatitis caused by a drug-induced autoimmune response.

Given the totality of evidence and the wide use of YKS in the Japanese health care system, this product appears to be very safe for clinical use, with less serious and less frequent adverse effects than the majority of pharmaceutical medications. Nevertheless, when YKS is used, attention should be paid to avoiding and detecting the adverse effects raised in this section.

Conclusion

YKS appears to have beneficial effects in a variety of diseases, most of which are either psychiatric in nature and/or occur with the aging process. Given the existing evidence and its traditional uses, YKS might be especially useful in clinical conditions accompanied by aggressiveness, impulsive behaviors, and/or involuntary movements. More research is required to further clarify the uses and effectiveness of YKS. In designing future trials, consideration should be given to enrolling participants who also meet the criteria for the use of this formula based on Kampo diagnosis.

In the past decade, YKS became accepted as a standard medicine for BPSD in Japan. It is also officially listed in the Japanese Guidelines for the Management of Dementia as a Grade C1 prescription (recommended regardless of insufficient scientific evidence) for the treatment of sleep disorders and BPSD (especially in DLB) by the Japanese Society of Neurology. This clinical area appears to be a highly promising area for further investigation, and for integration into health care systems outside of Japan. The other areas in which YKS has shown potential for clinical benefit require more clinical and basic studies before any definitive statements can be made about its efficacy and safety. One issue that must be kept in mind is the quality of YKS being used. As mentioned above, Kampo formulas in Japan are standardized and regulated to meet quality control standards akin to those for prescription drug medications. Most studies conducted to date have used YKS produced in Japan. This high degree of quality and standardization will not necessarily apply to YKS formulas made outside of Japan.

YKS is not the one and only Kampo formula used widely in the Japanese health care system. Other approved Kampo prescriptions also require additional study to document which might be effective as alternative or accessory treatments for various diseases refractory to conventional medicine as a sole intervention.

Disclosure

Japanese-Oriental medicine department receives fundings for scholarship activities from Kampo pharmaceutical companies but it is strictly prohibited to use those fundings for research at Chiba University. The authors report no conflicts of interest in this work.