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Review

Treating senile dementia with traditional Chinese medicine

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Pages 201-208 | Published online: 19 Oct 2022

Abstract

Senile dementia is a syndrome in the elderly involving deficits in memory and cognition. There has been a long history of research and medical practice in dementia in China, during which the ancient Chinese people have formed a whole theory and accumulated abundant experience in the treatment of dementia. During recent decades, with new theories and technologies being digested and integrated, progress has been made in the medical and pharmacy research on senile dementia in China. In this review, we will focus on the traditional opinion, clinical practice, and recent progress in pharmacological research in China towards the treatment of dementia. We also discuss the potential trends of global convergence.

The term “senile dementia” refers to a clinical syndrome seen in the elderly characterized by impairment of memory and cognition. With the dramatic improvement of average life expectancy and the fast increasing of the aged population in recent years, senile dementia has become a major problem of public health.

Alzheimer’s disease (AD) is the most common type of dementia, which is a progressive neurodegenerative disease and has become the third greatest threat to elderly, inferior only to cardiovascular disease and cancer. Since 1907, when German surgeon Alois Alzheimer reported the first case of dementia that now bears his name, great efforts have been made in attempt to discover the pathology and remedy of AD. Though neither consensus concerning pathogenesis nor perfect therapy is available at present, progress has been made. Pathological hallmarks of AD include extracellular deposition of senile plaques (SP), formation of intracellular neurofibrillary tangles (NFT), and lesions of cholinergic neurons together with synaptic alterations in cerebral cortex, hippocampus, and other brain regions essential for cognitive function. It is now well accepted that multiple factors, such as apoptosis, oxidative stress, excitotoxicity, and disturbance of energy metabolism homeostasis, contribute to the progression of AD. Another common form of dementia in the elderly is vascular dementia (VD). This disorder, like AD, presents as a clinical syndrome of intellectual impairment caused by cerebrovascular elements such as stroke, infarct, and hemorrhagic brain lesion. As the common downstream pathway of neurodegenerative disease, free radical damage-induced oxidative stress and apoptosis are involved in the VD pathology.

China is well known for its long history of traditional Chinese medicine (TCM), which has endured for thousands of years. Through persistent attempts and practice for generations, Chinese people have accumulated profound experience in disease prevention, diagnosis, and treatment, and formed a whole theoretical system of medicine and therapy. We will introduce the status and progress of dementia treatment in China with TCM in this review.

Progress in medication research

In the vast territory of China, smart and industrious Chinese people have made the best of immense natural resources for medical application. Herbal medicines of intellective and memory benefits were mentioned in some geography literature such as Shan Hai Jing and some medical literature like Ben Cao Gang Mu (Compendium of Materia Medica).

Over the past years, quite a number of viewpoints have been put forward with the intent of explaining theories of TCM in how dementia forms and develops. In general, loss of memory was indicated to come from atrophy and empty state of brain rather than heart, and was classified according to clinical symptoms. On one hand, kidney decline as well as blood decay results in brain dystrophy. Hence, herbal medicine like ginseng, fructus lycii, polygala, angelica can be used to supplement blood and nourish kidney. On the other hand, pent-up phlegm and retarded blood circulation can induce chaos and toxicity of brain. Accordingly, such herbals as glycyrrhiza, atractylodes, rhubarb, and safflower often served as expectorants and promoters for blood circulation. Furthermore, it was suggested that normal functioning of human body not only lies on the function of every single viscus, but, more importantly, depends on the harmony and balance between each apparatus. During recent decades, a growing numbers of preclinical and clinical studies have found efficiencies of some herbal extract, some specific combinations of herbals, and herbal tea in AD treatment. In this review we will discuss the pharmacologic profiles of some representative natural products.

Huperzine A

(–)-Huperzine A (HupA) is a novel Lycopodium alkaloid isolated from the Chinese medicinal herb Huperzia serrata (Qian Ceng Ta, ), which has been used by Chinese civilians for centuries in the treatment of such conditions as contusions, strains, swelling, and schizophrenia. As a chemically unique compound in comparison with other agents under study for AD, namely tacrine, galanthamine, donepezil, and rivastigmine, HupA is a reversible, potent, and selective acetylcholinesterase (AChE) inhibitor, and has been found to improve cognitive deficits in a broad range of animal models (CitationWang et al 2006a). Phase IV clinical trials conducted in China have demonstrated that HupA can significantly improve memory of elderly people and patients with AD and VD without any notable side effects (CitationXu et al 1995; CitationYang et al 2003).

Figure 1 Pictures of Chinese herbs and the parts effective in treating dementia. A: Huperzia serrata (Qian Ceng Ta); B: Panax ginseng C.A. Mey. (Ginseng), drawn by Zeng Li Li; C: Anemarrhena asphodeloides Bunge. (Zhimu), drawn by Chun Quan Xu; D: Rhodiola saccharinensis A. Bor. (Integripetal rhodiola herb); E: Salvia miltiorrhiza Bunge. (Danshen), drawn by Zeng Li Li; F: Pueraria lobata (Willd.) Ohwi (Radix Puerariae), drawn by Zeng Li Li. Panels B, C, E, and F are from (CitationLou and Xiao 1995). Panel D is from (CitationZhu 1999).

Figure 1 Pictures of Chinese herbs and the parts effective in treating dementia. A: Huperzia serrata (Qian Ceng Ta); B: Panax ginseng C.A. Mey. (Ginseng), drawn by Zeng Li Li; C: Anemarrhena asphodeloides Bunge. (Zhimu), drawn by Chun Quan Xu; D: Rhodiola saccharinensis A. Bor. (Integripetal rhodiola herb); E: Salvia miltiorrhiza Bunge. (Danshen), drawn by Zeng Li Li; F: Pueraria lobata (Willd.) Ohwi (Radix Puerariae), drawn by Zeng Li Li. Panels B, C, E, and F are from (CitationLou and Xiao 1995). Panel D is from (CitationZhu 1999).

In vitro and in vivo studies with respect to AChE inhibition demonstrated that AChE inhibition potency of HupA is similar or superior to those of inhibitors currently being used in AD treatment (CitationWang et al 1986; CitationWang and Tang 1998; CitationOgura et al 2000; CitationLiang and Tang 2004). Studies in our laboratory showed that in cortex, hippocampus, and striatum of mammalian brain, HupA exerts preferential inhibition against G4 (10S) AChE, which is the physiologically relevant form at cholinergic synapses and is the major form for metabolizing ACh (CitationZhao and Tang 2002).

Changes in oxidative metabolism are thought to be involved in such neurodegenerative disease as AD and ischemia/reperfusion-induced brain injury. Accumulated damage of cellular structure and function from free radicals are thought to result in oxidative stress and be involved in events that lead to neurodegeneration. HupA has been demonstrated by recent studies in our laboratory to protect against H2O2- and β-amyloid (Aβ)-induced cell lesion, decrease the level of lipid peroxidation, increase antioxidant enzyme activities in rat PC12 and NG108–15 cell lines and primary cultured cortical neurons (CitationXiao et al 1999, Citation2000a, Citation2000b, Citation2002; CitationZhang et al 2002), and protect against serum deprivation-induced toxicity (CitationZhou and Tang 2002), oxygen-glucose deprivation-induced toxicity (CitationZhou et al 2001b, Citation2001c), and ischemia-induced toxicity (CitationZhou et al 2001d; CitationWang et al 2006b), which may benefit AD and VD therapy. These protective effects involve, at least in part, the abilities of HupA to regulate apoptosis-related genes (CitationZhou et al 2001c), upregulate NGF secretion and its down-stream signaling (CitationTang et al 2005a, Citation2005b; CitationWang et al 2006b), inhibit oxidative stress, and improve energy metabolism (CitationGao and Tang 2006). We also found that HupA can modulate the processing of amyloid precursor protein (APP) in both rats infused intracerebroventricularly with Aβ1–40 and HEK293sw cell line, via regulating protein kinase C (PKC) (CitationZhang et al 2004). This effect might be beneficial for AD therapy, since it promotes the nonamyloidogenic pathway of APP metabolism and hence reduces the production of Aβ, and the nonamyloidogenic product itself, namely APPsα, is proved neuroprotective.

In the recent clinical trials carried out in China, HupA has demonstrated significant effect and safety in the treatment of neurodegenerative disease such as AD (CitationXu et al 1995; CitationYang et al 2003) and vascular dementia (CitationWei et al 2001; CitationYin et al 2001; CitationZhang and Fu 2001; CitationZhong and Liang 2004), as well as improvement of memory and cognitive deficits caused by other pathogenies, such as schizophrenia (CitationFang et al 2002; CitationMa et al 2003; CitationYang 2003), brain trauma (CitationZhou et al 2001a), and lack of iodine (CitationQu et al 1995). Clinical trials using HupA plus nilestriol (CitationWang et al 2003), or HupA plus nicergoline, aspirin as well as estrogen (CitationZhou et al 2004), have shown favorable results in both AD and VD patients. Clinical investigators also found that combination with function convalescence training, daily life activities training, or a specific mental stimulation program consisting of reminiscence, reality orientation and remotivation, can promote the effects of medicine treatment.

AD is a neurodegenerative disease with complicated pathogenesis, therefore therapy with multiple drugs or drugs with polypharmacological activities will likely be the best approache to address the varied pathological aspects of the disease. Encouraging preclinical and clinical findings suggest that HupA is a promising candidate for the treatment of neurodegenerative diseases such as AD and VD, and is very likely to exert its therapeutic effects via a multi-target mechanism.

Ginkgo biloba extract

Ginkgo biloba (Ginkgoaceae) is an ancient Chinese tree that has been cultivated and held sacred for its health-promoting properties. There is substantial experimental evidence to support the view that the leaf extract of Ginkgo biloba (EGb) has many pharmacological effects (CitationSierpina et al 2003). Pharmacological studies demonstrated that EGb can reverse yohimbine-induced spatial working memory deficit in rats (CitationZhang and Cai 2005), improve learning performance in cerebral ischemic mice (CitationTadano et al 1998), reduces infarct volume and cell apoptosis in cortex of ischemic mice (CitationUnal et al 2001), as well as reverse memory deficit and decline in choline actyltransferase activities in the hippocampus of rats infused intracerebroventricularly with Aβ1–40 (CitationTang et al 2002). In vitro studies showed that EGb can protect against apoptosis induced by hydroxyl radicals (CitationNi et al 1996; CitationWei et al 2000), against cell death induced by beta-amyloid (CitationBastianetto et al 2000a), and against nitric oxide-induced toxicity (CitationBastianetto et al 2000b). Mechanisms underlying these protective effects remain unclear. As we now know, EGb is a mixture of flavonoids, terpenes, and organic acids, etc. EGb and its constituent ginkgolide B were reported to attenuate glutamate-induced neuronal damage (CitationZhu et al 1997). EGb’s ability to decrease bax/bcl-2 ratios (CitationLu et al 2006), reverse ischemia-induced reductions in COX III mRNA in CA1 neurons prior to their death (CitationChandrasekaran et al 2001), inhibit nitric oxide synthesis (CitationCalapai et al 2000), scavenge free radicals (CitationMaitra et al 1995) and attenuate lipid peroxidation (CitationBridi et al 2001) might involve in its neuroprotective effects. A very recent study suggests that EGb has potent antioxidant activity and may play a role in the neuroprotective process by attenuating the ischemia/reperfusion-induced oxidative protein modification and lipoperoxidation (CitationUrikova et al 2006).

Along with the progress in pharmacological research, quite a few preparations of EGb have been developed and put into home and overseas market during recent years. At present EGb is used clinically for improving peripheral vascular diseases in France and Germany and is ingested widely as an herbal medicine in some countries. Double-blinded randomized controlled clinical trial has demonstrated the efficacy of EGb 761, the standardized preparation of EGb, in treatment for mild to moderate AD (CitationMaurer et al 1997). A 24-week, multicenter, double-blind, placebo-controlled, randomized trial confirmed that EGb 761 improves cognitive function in a clinically relevant manner in patients suffering from dementia (CitationKanowski and Hoerr 2003). Moreover, a very recent randomized placebo-controlled double-blind study showed that EGb 761 (160 mg/d) had a comparable efficacy with donepezil (5 mg/d) in treating mild to moderate AD, and also suggested the efficacy and tolerability of the Ginkgo biloba special extract (Flavogin) in the dementia of the Alzheimer type with special respect to moderately severe stages (CitationMazza et al 2006). Results from clinical trials in China demonstrated that treatment with EGb can significantly improve the cognitive function and living ability of patients with VD (CitationLi 2003; CitationZhang and Li 2003; CitationShi et al 2006), multi-infarct dementia (CitationWu et al 2001), and cerebral infarction dementia (CitationWu 2003). Moreover, the active component of EGb, such as ginkgo flavone glycoside, was also reported to be efficient and safe for VD treatment (CitationLi et al 2004a).

Radix ginseng

As a well known invigorant, there has been a long history of ginseng () application in China. Its active compounds, including total ginsenosides, ginsenoside Rg1, and panaxynol, were found to possess central cholinomimetic and catecholaminomimetic activity, and can modulate the balance of stimulating and inhibiting process in central nervous system as well as promote neuronal plasticity and neurogenesis. Researchers found that ginsenosides Rb1 and Rg3 exerted significant neuroprotective effects on cultured cortical cells against glutamate-induced neurodegeneration (CitationKim et al 1998), indicating it may be efficacious in protecting neurons from oxidative damage produced by exposure to excess glutamate. Furthermore, protopanaxadiol-type saponins were reported to enhance axonal and dendritic formation activity (CitationTohda et al 2002). Pharmacological studies have demonstrated that saponins can improve learning and memory in animals impaired with scopolamine (CitationNi et al 2000; CitationZhao et al 2000; CitationChen and Zhu 2005) and transient global ischemia (CitationShen and Zhang 2004), as well as protect brain function and postpone brain aging by decreasing free radicals damage and increasing activities of GSH-Px and SOD (CitationZhang et al 2003). The ability of ginsenoside to enhance TrkB expression might also be involved in its protective effect (CitationLai et al 2006). Using 3H-(-)nicotine displacement assay, Panax ginseng was found to have affinity for both the nicotinic receptor, and to a lesser extent the muscarinic receptor (IC50 2.12 mg/mL and 5.25 mg/mL respectively), and the activity of the plant extracts was excluded as resulting from choline (CitationLewis et al 1999), and the demonstrated nicotinic activity of ginseng warrants further investigation with reference to therapeutic activity in age-related conditions such as dementia.

Rhizoma anemarrhenae (Zhimu)

Rhizoma anemarrhenae () is a commonly used medicinal material for nourishment. The main active constituents include sarsasapogenin, smilagenin, neogitogenin, and markosapogenin. Pharmacological studies demonstrated that it can protect from learning and memory impairment induced by D-galactose (CitationChen et al 2000; CitationMa et al 2004), scopolamine, AlCl3 (CitationMa et al 2005), β-amyloid peptide (CitationChen et al 2001a; CitationOuyang et al 2005), ibotenic acid (CitationSun et al 2004), cholesteremia and ischemic brain injury (CitationDeng et al 2005), and enhance memory of normal aged animals (CitationHu et al 2003). These effects are very likely related with its activity of improving the synthetic speed of acetylcholine (ACh) and density of M-type ACh receptors (CitationChen et al 2001b, Citation2004; CitationHu et al 2001), scavenging free radicals (CitationChen et al 2000), upregulating brain-derived neurotrophic factor (BDNF) (CitationHu et al 2003), as well as antioxidation (CitationOuyang et al 2005).

Integripetal rhodiola herb (Rhodiola rosea L.)

Integripetal rhodiola herb () is a perennial plant of Rhodiola family with succulent rhizome. The essential component, rhodosin, is well known for protection against hypoxia and external injury. Recent studies have found that rhodosin or the crude extract can protect from learning and memory impairment induced by D-galactose (CitationXie et al 2003), scopolamine (CitationWu et al 2004b), β-amyloid peptide (CitationXie et al 2004), hypoxia (CitationLiu et al 2003), and cerebral ischemia-reperfusion (CitationSong et al 2005). Rhodosin can also enhance memory of normal-aged rats (CitationJiang et al 2001). Its ability to increase ACh content and reduce cholinesterase activity in the brain (CitationWu et al 2004b) and antioxidation activity (CitationJiang et al 2001) might contribute to preventing neurodegenerative changes.

Danshen root (Salvia miltiorrhiza Bunge.)

Danshen root () is a kind of medical material with activity of blood flow promotion and blood-stasis elimination, which has been frequently used for cardiovascular and hematological disorders in China. One of its constituent, namely tanshinone, can improve cholinergic functions in central nervous system (CitationLi et al 2004b) and inhibit inflammatory reaction by inhibiting the expression of pro-inflammatory cytokines (CitationHu et al 2006) and inducible nitrogen oxidase (iNOS) (CitationLi et al 2004b). Salvianolic acid, another essential component, is an antioxidant (CitationHuang and Zhang 1992) found to protect from ischemic brain injury (CitationWu et al 2000).

Radix puerariae (Pueraria lobata [Willd.] Ohwi)

Various medical properties of Radix puerariae () have been documented over 2000 years. Flavone extracted from its radix and leaves are found to be of multiple health benefits. The active component, puerarin, proved to widen coronary artery and cerebral artery and help lower blood pressure. Recent studies revealed that puerarin can protect from learning and memory impairment induced by D-galactose (CitationXu and Zhao 2002), scopolamine (CitationHsieh et al 2002), β-amyloid peptide (CitationYang et al 2005), ischemic brain injury (CitationWu et al 2004a), and chronic alcoholism (CitationSun 2005).

Green tea

The history of cultivating and drinking green tea in China is centuries old. Green tea is a popular beverage and is now widely believed to promote blood flow, lower blood fat, and help weight-loss. Recently, dietary components with antioxidant activity have attracted particular attention for their potential role in modulating oxidative stress associated with aging and chronic conditions. Consistent with epidemiological studies, recent research indicates that the antioxidant properties of polyphenols, the active components enriched in green tea, may contribute to reducing the risk of cardiovascular disease, cancer, and dementia (CitationYan and Wu 2001; CitationLi et al 2006), which are the leading causes of morbidity and mortality among the elderly (CitationMeydani 2001). The in vitro anti-beta-secretase and dual anticholinesterase activities of green tea was reported recently, indicating that tea contains active agents, which may function synergistically, to retard progression of the diseases, assuming that these agents, yet to be identified, reach the brain (CitationOkello et al 2004).

Clinical studies

Though the term “senile dementia” did not appear in the traditional Chinese medical literature, ancient medics were conscious of the phenomena and depicted elaborately its clinic exhibitions in medical books, including memory letdown, vacant face expression, lack of responsiveness and decline of intellectual ability such as comprehension and judgment, as well as emotional abnormity. Over 2000 years before, there were remarks of dementia and forgetfulness in the oldest medical book in China, Huang Di’s Canon of Internal Medicine. With the development of modern medicine, people are more acquainted with dementia. More and more new therapeutic programs are put forward and tested during the course of clinical practice, such as combination therapy using drugs of different pharmacological profiles, or using drugs in combination with mental training.

Assisting therapy and prevention

Most patients with dementia are looked after by family in China. Therefore lifestyle can influence the efficacy of clinical therapy to a certain degree, and access to social guidance, consultants, and assistance can be of a large beneft to the dementia patient. More people are beginning to realize the importance of a regular and disciplined healthy lifestyle. The daily diet is acquiring accumulating attention for its potential influence on health condition. With the development of imageology and neuropsychology, diagnosis and classification of dementia are becoming easier and more accurate. Patients with dementia now have access to more reasonable and scientific diagnosis, treatment, and nursing.

Summary

Chinese people have studied and fought with dementia for a long period of time. An immense experience and systematic theory of treating dementia has been accumulated during the long history of development of TCM. Nowadays part of the experience is still relevant. With the global application of modern science and technology, more and more natural resources and products from TCM are being studied and recognized. The resources and experience of TCM will continue to play an important role in the fight against aging and dementia.

References

  • BastianettoSRamassamyCDoreS2000aThe Ginkgo biloba extract (EGb 761) protects hippocampal neurons against cell death induced by beta-amyloidEur J Neurosci1218829010886329
  • BastianettoSZhengWHQuirionR2000bThe Ginkgo biloba extract (EGb 761) protects and rescues hippocampal cells against nitric oxide-induced toxicity: involvement of its flavonoid constituents and protein kinase CJ Neurochem7422687710820186
  • BridiRCrossettiFPSteffenVM2001The antioxidant activity of standardized extract of Ginkgo biloba (EGb 761) in ratsPhytother Res154495111507743
  • CalapaiGCrupiAFirenzuoliF2000Neuroprotective effects of Ginkgo biloba extract in brain ischemia are mediated by inhibition of nitric oxide synthesisLife Sci6726738311105983
  • ChandrasekaranKMehrabianZSpinnewynB2001Neuroprotective effects of bilobalide, a component of the Ginkgo biloba extract (EGb 761), in gerbil global brain ischemiaBrain Res9222829211743961
  • ChenQCaoYGLinYM2004Effects of sapogenin from zhimu (ZMS) and its isomer on learning and memory ability and muscarinic subtype M1 receptor density in aged ratsChin Pharmacol Bull205614
  • ChenQHuYEXiaZQ2000Action of Sapogenin from Zhimu on learning and memory ability and free-radical metabolism in mouse D-galactose demetia modelPharmacol Clin Chin Mater Med161416
  • ChenQHuYEXiaZQ2001aEffect of ZMS on demented model by injection of beta-amyloid to right nucleus basalisActa Univ Med Second Shanghai214013
  • ChenQHuYEXiaZQ2001bThe effects of ZMS on learning and memory ability and brain choline acetyltransferase in scopolamine-induced mouse modelJ Chin Med Mater244968
  • ChenXMZhuJB2005Effects and mechanisms of ginsenoside Rg1 on learning and memory impairment induced by scopolamine hydrobromideChin J Pharmacol Ther10898902
  • DengYMaBPXuQP2005Effect and mechanism of effective component in Zhimu on ability of learning and memory in vascular dementia ratsChin Pharmacol Bull218303
  • FangCXGuoCRWuB2002Effect of huperzine A on memory of schizophrenia patientsShandong Arch Psychiatry153940
  • GaoXTangXC2006Huperzine A attenuates mitochondrial dysfunction in beta-amyloid-treated PC12 cells by reducing oxygen free radicals accumulation and improving mitochondrial energy metabolismJ Neurosci Res8310485716493671
  • HsiehMTKuoLHTsaiFH2002Effects of puerarin on scopolamine-, mecamylamine-, p-chloroamphetamine- and dizocilpine-induced inhibitory avoidance performance impairment in ratsPlanta Med68901512391553
  • HuMHuYEZhangW2001The effect of ZMS on brain M receptor in aged ratsChin J Nucl Med2115861
  • HuXMZhouMMHuXM2006The effects of sodium β-aescinate on inflammatory process induced by focal cerebral ischemia -reperfusion in ratsChin Pharmacol Bull2243640
  • HuYESunQXXiaZQ2003The effect of ZMS, an active component of Zhimu on NGF and BDNF in brains of aged ratsChin Pharmacol Bull1914951
  • HuangYSZhangJT1992In vitro antioxidant effects of three water-soluble components isolated from Salvia miltiorrhizaActa Pharm Sin2796100
  • JiangWHMengXTHaoLM2001Study of anti-aging and anti-dementia effects of Rhodosin on aging rats and experimental dementia ratsJ N Bethune Univ Med Sci271279
  • KanowskiSHoerrR2003Ginkgo biloba extract EGb 761 in dementia: intent-to-treat analyses of a 24-week, multi-center, double-blind, placebo-controlled, randomized trialPharmacopsychiatry3629730314663654
  • KimYCKimSRMarkelonisGJ1998Ginsenosides Rb1 and Rg3 protect cultured rat cortical cells from glutamate-induced neurodegenerationJ Neurosci Res53426329710262
  • LaiHZhaoHHZengL2006Effects of ginsenosides on the expression of TrkB mRNA in hippocampal formation of aged ratsChin Pharmacol Bull223418
  • LewisRWakeGCourtG1999Non-ginsenoside nicotinic activity in ginseng speciesPhytother Res13596410189953
  • LiBWangBCYangWH2006Effects of green tea polyphenols on learning behavior and AChE activity of mice with Alzheimer’s diseaseJ Beihua Univ (Nat Sci)74750
  • LiDXZhangDMLiuJX2004aTreatment of 43 cases of vascular dementia with Ginkgo flavone glycosideHerald Med23912
  • LiLXDaiJPRuLQ2004bEffects of tanshinone on neuropathological changes induced by amyloid beta-peptide(1–40) injection in rat hippocampusActa Pharmacol Sin25861815210058
  • LiYB2003Treatment of 92 cases of vascular dementia with ginkgo leaf tabletJ Pra Traditional Chin Intern Med172723
  • LiangYQTangXC2004Comparative effects of huperzine A, donepezil and rivastigmine on cortical acetylcholine level and acetylcholinesterase activity in ratsNeurosci Lett36156915135892
  • LiuZWWuMCChenP2003Effects of Rhodiola henryi extract on learning, memory and antihypoxia in miceActa Nutr Sin251014
  • LouZCXiaoPG1995Commonly used traditional Chinese medicineQianXZColored illustrated book of Chinese Materia MedicaBeijingPeople’s Medical Publishing House
  • LuGWuYMakYT2006Molecular evidence of the neuroprotective effect of Ginkgo biloba (EGb761) using bax/bcl-2 ratio after brain ischemia in senescence-accelerated mice, strain prone-8Brain Res109023816677616
  • MaJDZhengHWangYJ2003Effect of huperzine on the memory disoders of schizophrenia patient during rehabilitation periodHealth Psychol J113401
  • MaYQLiLLiuGB2005The effects of SAaB on Alzheimer’s model rats indeced by AlCl3Qilu Affair246256
  • MaYQZhouXMWangLH2004Anti-aging action of saponins from Anemarrhena asphodeloides Bge. on D-galactose model miceJ Shenyang Pharma Univ214503
  • MaitraIMarcocciLDroy-LefaixMT1995Peroxyl radical scavenging activity of Ginkgo biloba extract EGb 761Biochem Pharmacol491649557786306
  • MaurerKIhlRDierksT1997Clinical efficacy of Ginkgo biloba special extract EGb 761 in dementia of the Alzheimer typeJ Psychiatr Res31645559447569
  • MazzaMCapuanoABriaP2006Ginkgo biloba and donepezil: a comparison in the treatment of Alzheimer’s dementia in a randomized placebo-controlled double-blind studyEur J Neurol13981516930364
  • MeydaniM2001Nutrition interventions in aging and age-associated diseaseAnn N Y Acad Sci9282263511795514
  • NiXHBaiJLuYQ2000Studies on effect of crude saponin extracted from Panax ginseng root or stem and leaf on improving the learn and memory-barrier of ratsLishizhen Med Materia Medica Res117735
  • NiYZhaoBHouJ1996Preventive effect of Ginkgo biloba extract on apoptosis in rat cerebellar neuronal cells induced by hydroxyl radicalsNeurosci Lett214115188878097
  • OguraHKosasaTKuriyaY2000Comparison of inhibitory activities of donepezil and other cholinesterase inhibitors on acetylcholinesterase and butyrylcholinesterase in vitroMethods Find Exp Clin Pharmacol226091311256231
  • OkelloEJSavelevSUPerryEK2004In vitro anti-beta-secretase and dual anti-cholinesterase activities of Camellia sinensis L. (tea) relevant to treatment of dementiaPhytother Res18624715476306
  • OuyangSSunLSGuoSL2005Effects of timosaponins on learning and memory abilities of rats with dementia induced by lateral cerebral ventricular injection of amyloid β-peptideJ First Mil Med Univ251216
  • QuCYWangHMYuW1995A pilot report on huperzine A in treating amentia in iodine-lacking areaShanxi Med J24478
  • ShenLHZhangJT2004Ginsenoside Rg1 increases the survival rate of hippocampal neural stem cells and improves learning and memory in gerbils suffered from transient global ischemiaCentral South Pharmacy269
  • ShiGPPanDHeXQ2006Clinical study on the treatment of vascular dementia patients with tablets of extract from Ginkgo leavesMed J Chin People Health18199200
  • SierpinaVSWollschlaegerBBlumenthalM2003Ginkgo bilobaAm Fam Physician68923613678141
  • SongYYQiGHanJT2005Protective effect of hongjingtian on hippocampal area and dentate gyrus of complete cerebral ischemia-reperfusion in ratsChin J Clin Rehabil92323
  • SunQXHuYEGuanH2004Effects of ZDY101, an active component from Zhimu, on rat dementia model produced by intracranial injection of ibotenic acidNucl Tech27297300
  • SunX2005Observation of 68 cases on effects of puerarin on the chronic alcoholismJ Linyi Med Coll272912
  • TadanoTNakagawasaiOTan-noK1998Effects of ginkgo biloba extract on impairment of learning induced by cerebral ischemia in miceAm J Chin Med26127329799964
  • TangFNagSShiuSY2002The effects of melatonin and Ginkgo biloba extract on memory loss and choline acetyltransferase activities in the brain of rats infused intracerebroventricularly with beta-amyloid 1–40Life Sci7126253112354581
  • TangLLWangRTangXC2005aEffects of huperzine A on secretion of nerve growth factor in cultured rat cortical astrocytes and neurite outgrowth in rat PC12 cellsActa Pharmacol Sin26673815916732
  • TangLLWangRTangXC2005bHuperzine A protects SHSY5Y neuroblastoma cells against oxidative stress damage via nerve growth factor productionEur J Pharmacol51991516111675
  • TohdaCMatsumotoNZouK2002Axonal and dendritic extension by protopanaxadiol-type saponins from ginseng drugs in SK-N-SH cellsJpn J Pharmacol902546212499580
  • UnalIGursoy-OzdemirYBolayH2001Chronic daily administration of selegiline and EGb 761 increases brain’s resistance to ischemia in miceBrain Res9171748111640903
  • UrikovaABabusikovaEDobrotaD2006Impact of Ginkgo biloba extract EGb 761 on ischemia/reperfusion-induced oxidative stress products formation in rat forebrainCell Mol Neurobiol26134151
  • WangHTangXC1998Anticholinesterase effects of huperzine A, E2020, and tacrine in ratsActa Pharmacol Sin192730
  • WangRYanHTangXC2006aProgress in studies of huperzine A, a natural cholinesterase inhibitor from Chinese herbal medicineActa Pharmacol Sin2712616364207
  • WangRQLeiQYGuJQ2003Nilestriol combined with huperzine in improving cognition of female patients with Alzheimer’s diseaseChin J Clin Rehabil715389
  • WangYEYueDXTangXC1986Anti-cholinesterase activity of huperzine AActa Pharmacol Sin711013
  • WangZFTangLLYanH2006bEffects of huperzine A on memory deficits and neurotrophic factors production after transient cerebral ischemia and reperfusion in micePharmacol Biochem Behav836031116687166
  • WeiTNiYHouJ2000Hydrogen peroxide-induced oxidative damage and apoptosis in cerebellar granule cells: protection by Ginkgo biloba extractPharmacol Res414273310704267
  • WeiYFHeJYSongFG2001Observation on clinical effect of huperzine A on 50 vascular dementia patientsShandong Med J41256
  • WuHQChangMZZhangGL2004aThe mechanism of protective effects of puerarin on learning-memory disorder after global cerebral ischemic reperfusive injury in ratsJ Apoplexy Nerv Dis213503
  • WuJFWangJZhangJT2000Effects of total salvianolic acid on focal cerebral ischemic injury and antioxidase activitiesChin New Drug J94525
  • WuSDLuWJWangF2001Clincal observation of treating multi-infarct dementia with standardized extract of Ginkgo bilobaNerv Dis Ment Hyg1412
  • WuYQYaoWBGaoXD2004bEffects of the extracts of Rhodiola rosea L. on improving the ability of learning and memory in miceJ China Pharm Univ356972
  • WuZX2003Clinical analysis of ginkgo leaf therapy for cerebral infarction Alzheimer’s diseaseChin J Med Writing1012045
  • XiaoXQWangRHanYF2000aProtective effects of huperzine A on beta-amyloid(25–35) induced oxidative injury in rat pheochromocytoma cellsNeurosci Lett286155810832008
  • XiaoXQWangRTangXC2000bHuperzine A and tacrine attenuate beta-amyloid peptide-induced oxidative injuryJ Neurosci Res61564910956426
  • XiaoXQYangJWTangXC1999Huperzine A protects rat pheochromocytoma cells against hydrogen peroxide-induced injuryNeurosci Lett27573610568502
  • XiaoXQZhangHYTangXC2002Huperzine A attenuates amyloid beta-peptide fragment 25–35-induced apoptosis in rat cortical neurons via inhibiting reactive oxygen species formation and caspase-3 activationJ Neurosci Res6730611754078
  • XieGQSunXLTianSP2003Studies on the preventive and therapeutic effects of rhodosin on rats with Alzheimer’s diseaseChin J Behav Med Sci121820
  • XieGQSunXLTianSP2004Preventive effects of rhodosin and melatonin from damage induced by β-amyloid 1–40 in senile ratsJ Nanjing Med Univ182036
  • XuSSGaoZXWengZ1995Efficacy of tablet huperzine-A on memory, cognition, and behavior in Alzheimer’s diseaseActa Pharmacol Sin163915
  • XuXHZhaoTQ2002Effects of puerarin on D-galactose-induced memory deficits in miceActa Pharmacol Sin235879012100749
  • YanLWuS2001Studies on the early prevention of teapolyphenol on senile dementiaZhejiang J Integ Trad Chin West Med1153840
  • YangCYLvZPZhengCG2003Efficacy and reliability of huperzine A in mild and moderate Alzheimer’s diseaseChin J Clin Rehabil742589
  • YangDXTangYHuXM2005Effects of puerarin on learning and memory of model mouse with beta amyloid peptide-induced dementiaChin J Clin Rehabil916971
  • YangJZ2003Effect of huperzine A on the memory deficits of schizophrenia patients during rehabilitation periodChin J Clin Rehabil71440
  • YinFMDuYYWangLE2001Analyze of intervention effect of huperzine A on vascular dementiaMod Rehabil5745
  • ZhangDMLiDX2003The efficacy of Ginkgo leaf preparation treating vascular dementiaPr Geriatr171979
  • ZhangHYLiangYQTangXC2002Stereoselectivities of enantiomers of huperzine A in protection against beta-amyloid(25–35)-induced injury in PC12 and NG108–15 cells and cholinesterase inhibition in miceNeurosci Lett317143611755260
  • ZhangHYYanHTangXC2004Huperzine A enhances the level of secretory amyloid precursor protein and protein kinase C-alpha in intracerebroventricular beta-amyloid-(1–40) infused rats and human embryonic kidney 293 Swedish mutant cellsNeurosci Lett36021415082169
  • ZhangJSFuYQ2001Observation on effect of huperzine A on 50 vascular dementia patientsJ Pr Med Tech8882
  • ZhangMCaiJ2005Extract of Ginkgo biloba leaves reverses yohimbine-induced spatial working memory deficit in ratsBehav Pharmacol16651616286817
  • ZhangQHSunWJJuBZ2003Effect of ginseng stem-leaf saponin on mice’s brain agingChin Traditional Pat Med2521619
  • ZhaoQTangXC2002Effects of huperzine A on acetylcholinesterase isoforms in vitro: comparison with tacrine, donepezil, rivastigmine and physostigmineEur J Pharmacol455101712445575
  • ZhaoXMZongRYXieXL2000Effects of ginsenoside of stem and leaf in combination with choline on learning and memoryActa Nutr Sin2226670
  • ZhongZGLiangKZ2004Clinical observation of effect of huperzine A on 29 vascular dementia patientsJ Hainan Med Coll1025152
  • ZhouBHSunZJXuF2001aDouble-blind study on huperzine A and Piracetan in treating amnesia induced by brain traumaJ Brain Nerv Dis91745
  • ZhouBRXuZQKuangYF2004Effectiveness of polydrug therapy for senile dementiaChin J Clin Rehabil8121415
  • ZhouJFuYTangXC2001bHuperzine A and donepezil protect rat pheochromocytoma cells against oxygen-glucose deprivationNeurosci Lett30653611403956
  • ZhouJFuYTangXC2001cHuperzine A protects rat pheochromocytoma cells against oxygen-glucose deprivationNeuroreport122073711447310
  • ZhouJTangXC2002Huperzine A attenuates apoptosis and mitochondria-dependent caspase-3 in rat cortical neuronsFEBS Lett52621512208497
  • ZhouJZhangHYTangXC2001dHuperzine A attenuates cognitive deficits and hippocampal neuronal damage after transient global ischemia in gerbilsNeurosci Lett3131374011682146
  • ZhuLWuJLiaoH1997Antagonistic effects of extract from leaves of ginkgo biloba on glutamate neurotoxicityActa Pharmacol Sin183447
  • ZhuTC1999Alpine plants of Changbaishan Mountain in ChinaBeijingScience Publishing Press