Baicalein improves behavioral dysfunction induced by Alzheimer’s disease in rats

Abstract

Background

Alzheimer’s disease (AD) is considered to be a neurodegenerative disorder that is characterized by increased oxidative stress. Medicinal plants, with their antioxidant properties, have been used to cure several human diseases. The aim of the current study was to explore the protective and therapeutic effect of baicalein on AD-induced rats.

Materials and methods

Swiss Wistar rats were used in the study. The rats were divided into five groups. Group I: normal control group treated with water; Group II: disease control treated with AlCl₃ to induce the mimicking AD for 4 successive weeks (SW); Group III: normal control group treated with baicalein (5 mg/kg) for 2 SW followed by combination of baicalein and AlCl₃ for 4 SW; Group IV: normal control group treated with baicalein (10 mg/kg) for 2 SW followed by combination of baicalein and AlCl₃ for 4 SW; Group V: normal control group treated with rivastigmine (0.3 mg/kg) for 2 SW followed by combination of rivastigmine and AlCl₃ for 4 SW. Moreover, the therapeutic groups are as follows: Group VI: AD disease control treated with AlCl₃ for 4 SW and serving as the therapeutic positive group; Group VII: AD disease control + baicalein (5 mg/kg) for 12 SW; Group VIII: AD disease control + baicalein (10 mg/kg) for 12 SW; Group IX: AD disease control + rivastigmine (0.3 mg/kg) for 12 SW. Behavioral test, T-maze, and rotarod test were also performed before and after the treatment. At the end of the experimental study, all the rats were sacrificed and their brains were removed and divided into two portions. The first portion was homogenated for estimating the level of acetylcholinesterase (AchE) and acetylcholine (Ach). Another portion was used for histopathological evaluation.

Results

The current investigation showed that baicalein significantly reduced the duration of revolving on the rotarod, cage activity, and T-maze activity in a dose-dependent manner compared with the AD control group rats. It also altered the AchE and Ach levels in the brain homogenates. The histopathology study also provides strength to the protective effect of baicalein.

Conclusion

The current study showed that baicalein significantly (P<0.05) improved the biochemical and histopathological condition of AD in rats.

Keywords:

• baicalein
• Alzheimer’s disease
• acetylcholinesterase
• acetylcholine

Introduction

Alzheimer’s disease (AD) is a neurodegenerative disorder that is characterized by the progressive degeneration of cortical neurons and hippocampal cells, which has a negative effect on cognitive and memory function. The first clinical sign of the disease is the deterioration of short-term memory, whereas recovery of distant memories occurs relatively late in the course of the disease. At the onset of the disease, additional cognitive capabilities are impaired, as is the capability to analyze, and use common tools and objects. Senile plaques are the pathological hallmarks of AD, which are special depositions of protein β-amyloid characterized by the formation of neurofibrillary tangles and neuronal processes, composed of paired helical filaments and various proteins.^1,2

The selective deficiency of acetylcholine (Ach) in AD has given rise to the “cholinergic hypothesis”, which proposes that deficiency of Ach is critical for the genesis of the symptoms of AD. Therefore, a major approach to the treatment of AD involves attempts to augment the cholinergic function of the brain. This involves the use of cholinesterase inhibitors such as tacrine, galantamine, rivastigmine, and donepezil. Moreover, other hypotheses state that inflammation plays a key role in the pathogenesis of AD. In addition, excessive levels of reactive oxygen species are implicated in the etiology of AD.

Baicalein (5,6,7-trihydroxy-2-phenyl-4H-1-benzopyran-4-one), a flavonoid commonly known as Huangqin (China) and Ogon (Japan), is extracted from Scutellaria baicalensis. Various investigations have confirmed that baicalein has an anti-inflammatory, antidiabetic, antibacterial, antimicrobial, and anticancer effects. Moreover, its scavenging effects on various free radicals provide evidence of its antioxidant properties.

Medicinal plants have traditionally been used to treat several human diseases, and their pharmacological and therapeutic properties have been attributed to different chemical constituents isolated from their crude extracts. In particular, chemical constituents with antioxidant activity can be found at high concentrations in plants and can be responsible for their protective effects against various degenerative diseases, including cancer and neurological and cardiovascular disease. Thus, the antioxidant properties of plants have a full range of prospective applications in human health care.

Materials

Baicalein and aluminum chloride (AlCl₃) were purchased from Sigma-Aldrich Co., St Louis, MO, USA.

Animals

In the current study, we used the Swiss albino Wistar rats (male). The Wistar rats (140–190 g) were obtained from our institutional animal house. The rats were kept in a single cage in the departmental animal house under standard laboratory conditions (temperature 22°C±5°C, 12 hour dark/light cycles and artificially illuminated). The rats received a standard diet and water ab libitum during the acclimation time (1 week). This study was approved by the Sun-Yat Sen University Animal Ethical Committee and the study was performed in accordance with the committee’s guidelines for animal experiments.

Experimental study

During the experiment, the rats were divided into nine groups, with each group comprising 10 rats.

Protective groups

• Group I: Normal control group treated with water.

• Group II: Disease control group treated with AlCl₃ to induce the mimicking of AD for 2 successive weeks.

• Group III: Normal control group treated with baicalein (5 mg/kg) for 2 successive weeks, followed by a combination of baicalein and AlCl₃ for 4 successive weeks.

• Group IV: Normal control group treated with baicalein (10 mg/kg) for 2 successive weeks, followed by a combination of baicalein and AlCl₃ for 4 successive weeks.

• Group V: Normal control group treated with rivastigmine (0.3 mg/kg) for 2 successive weeks, followed by a combination of rivastigmine and AlCl₃ for 4 successive weeks.

Therapeutic groups

• Group VI: AD disease control group treated with AlCl₃ for 4 successive weeks and serving as the therapeutic positive group.

• Group VII: AD disease control group + baicalein (5 mg/kg) for 12 successive weeks.

• Group VIII: AD disease control + baicalein (10 mg/kg) for 12 successive weeks.

• Group IX: AD disease control + rivastigmine (0.3 mg/kg) for 12 successive weeks.

Behavioral stress tests

In the behavioral stress tests (the rotarod test and the cage test), the percentage behavior change was estimated using a square root transformation. This calculation was used to mitigate against the normal biological variations of the control rats in each group. Later, the square root transformed changes for each rat were compared with the baseline activity at each transitional step for the entire experimental study.

Estimation of motor coordination using the rotarod test

In the current investigation, the level of motor coordination was appraised using the accelerating rotarod test according to the method described by Mahdy et al,³ with minor modification.

Estimation of cognitive capabilities using T-maze test

The T-maze test was used to estimate the cognitive capability of the rats according to the method described by Deacon and Rawlins, with minor modification.⁴

Cage test

The cage test was used to estimate the movement of the rats according to the method described by Tsakiris et al,⁵ with minor modification.

Brain tissue preparation

At the end of the experimental study, all the rats were fasted overnight and killed by decapitation. For each group, the rat brain was immediately removed, washed in isotonic saline, and weighed. Next, the rat brain was divided into two portions. The first brain portion of each rat was homogenized in ice-cold medium (300 mmol/L sucrose and 50 mmol/L Tris–Hcl [pH =7.4]). The homogenate was centrifuged at 5,000 rpm for 5 minutes at 25°C. The collected supernatant was used to estimate biochemical parameters such as total protein, acetylcholinesterase (AchE), and Ach. The other portion of brain tissue was fixed in 10% formalin for histopathological observation.

Biochemical estimation

A choline/Ach assay kit was used to estimate the level of brain Ach, according to the manufacturer’s instructions. A colorimetric method was used to estimate the level of brain AchE. The brain protein concentration was determined (to express the level of protein in the brain) using the method described by Lowry et al.⁶

Western blot analysis

Using western blot analysis, cortical and hippocampal tissues were homogenized using ice-cold buffer. All the tissues were homogenized by high-speed centrifugation at 12,000 rpm for 20 minutes. The 50 µg/mL protein samples underwent sodium dodecyl sulfate (10%) polyacrylamide gel electrophoresis, after which the gel was transferred to polyvinylidene difluoride membrane. The prepared membrane was then incubated for 2 hours to remove the nonspecific binding site. Next, different proteins – namely, β-actin, γ and β secretases, β-amyloid, and amyloid precursor protein (APP) – were used.

Histopathological examination

The second portion of the rat brain from each group was fixed in buffer formalin (10%) for 24 hours. The brain tissue was washed in tap water and then dehydrated using serial dilutions of alcohol (ethyl, methyl, and absolute ethyl). The prepared tissue was cleared with xylene and embedded in paraffin for 24 hours, then a microtome was used to cut paraffin bees wax tissue blocks. The prepared tissue sample was placed on a glass plate, deparaffinized, and stained with eosin and hematoxylin strains for histopathological observation under a light microscope.

Results

Protective effect

Cage activity

Figure 1 shows the significant reduction in cage activity of the rats treated with AlCl3 after 4 weeks, compared with the activity of the baseline group of the same group. The AlCl3 control group rats treated with baicalein and rivastigmine showed increased activity in a dose-dependent manner. Baicalein (5 mg/kg) group rats showed an increase in cage activity compared with the AlCl₃ group rats. Baicalein (10 mg/kg) group rats showed a more marked effect. However, the rivastigmine group rats showed marked improvement in activity compared with the AlCl₃ group.

Figure 1 Protective effects of baicalein and rivastigmine on the levels of activity in AD-induced rats in activity cages.

Notes: All data are expressed as mean of movements ± SE. ^a% change; ^bsquare root transformed % change; ^csignificantly different from baseline of the same group at P<0.05; ^dsignificantly different from AD group at P<0.05; ^esignificantly different from rivastigmine when each is used for 4 weeks in combination with AlCl₃ at P<0.05; ^fsignificantly different from same group when given alone for 2 weeks at P<0.05.
Abbreviations: AD, Alzheimer’s disease; SE, standard error.

Effect on T-maze activity

The T-maze test result showed a significant increase in the time taken by the AlCl₃ group rats to reach the food over 4 successive weeks. Figure 2 shows that the AlCl₃ group rats treated with baicalein and rivastigmine showed a reduction in the time taken by the rats to reach the food compared with the time taken by the AD group rats.

Figure 2 Protective effects of baicalein and rivastigmine on the time taken to find the food in the T-maze by AD-induced rats.

Notes: All data are expressed in seconds as mean ± SE. ^aSignificantly different baseline duration of the same group at P<0.05; ^bsignificantly different from AlCl₃ after 4 weeks induction at P<0.05.
Abbreviations: AD, Alzheimer’s disease; SE, standard error.

Effect on rotarod activity

Figure 3 shows that the AD group rats treated with baicalein and rivastigmine showed no significant change in motor coordination in the rotarod test when compared with the baseline value groups. The result demonstrated that there were no significant changes in duration of sustained balance for the rats over 4 successive weeks.

Figure 3 Protective effects of baicalein and rivastigmine on the time spent on the rotarod by AD-induced rats.

Abbreviation: AD, Alzheimer’s disease.

Biochemical parameters

Figure 4 shows a significant reduction in the Ach levels found, and also confirms the enhanced level of AchE in the brain of the rats treated with AlCl₃ compared with those in the normal control group rats over 4 successive weeks. AlCl₃-treated rats that received baicalein showed a significant improvement in the level of Ach, and a reduction in the level of AchE, in a dose-dependent manner. However, rivastigmine showed a remarkable enhancement in the level of Ach, and reduction in the level of AchE, compared with the AD control group rats.

Figure 4 Protective effects of baicalein and rivastigmine on brain levels of (A): acetylcholine and (B): acetylcholinesterase in AD-induced rats.

Notes: All data are expressed as mean ± SE. ^#P<0.05 compared with the control group; *P<0.05, **P<0.01, and ***P<0.001 compared with the AD control group rats.
Abbreviations: AD, Alzheimer’s disease; SE, standard error.

Therapeutic effects

Cage activity

Figure 5 shows the effect of baicalein and rivastigmine on the AD-induced rats. The administration of baicalein (5 and 10 mg/kg) resulted in no significant change in activity compared with the baseline activity of the same group, but baicalein enhanced cage activity compared with the same group before treatment. However, the administration of rivastigmine also showed a significant increase in cage activity.

Figure 5 Protective effects of baicalein and rivastigmine on the levels of activity in AD-induced rats in activity cages.

Notes: All data are expressed as mean of movements ± SE. ^a% change; ^bsquare root transformed % change; ^csignificantly different from baseline of the same group at P<0.05; ^dsignificantly different from AD group at P<0.05; ^esignificantly different from same group when given alone for 2 weeks at P<0.05.
Abbreviations: AD, Alzheimer’s disease; SE, standard error.

Rotarod activity

Figure 6 shows that motor coordination activity was significantly reduced in the AD group rats, as tested by the rotarod, when the rats were treated with AlCl₃ for 4 successive weeks. The AD group rats treated with the baicalein underwent a significant improvement in motor coordination activity in a dose-dependent manner.

Figure 6 Protective effects of baicalein and rivastigmine on the time taken to find the food in the T-maze by AD-induced rats.

Notes: All data are expressed in seconds as mean ± SE. ^aSignificantly different baseline duration of the same group at P<0.05; ^bsignificantly different from AlCl₃ after 4 weeks induction at P<0.05; ^csignificantly different from baseline of the same group at P<0.05; ^dsignificantly different from AD group at P<0.05; ^esignificantly different from rivastigmine when each is used for 4 weeks in combination with AlCl₃ at P<0.05; ^fsignificantly different from same group when given alone for 4 weeks at P<0.05; ^gcompared with the baicalein (10 mg/kg).
Abbreviations: AD, Alzheimer’s disease; SE, standard error.

T-maze activity

In this test, the AlCl₃ (AD control) group rats showed a significant increase in the duration of time to reach the food over 4 successive weeks. The rats were left for 12 weeks without treatment and also treated with baicalein and rivastigmine. The AD rats treated with baicalein and rivastigmine showed a significant reduction in the time taken to reach the food in the T-maze test (Figure 7).

Figure 7 Protective effects of baicalein and rivastigmine on the time spent on the rotarod by AD-induced rats.

Notes: ^aSignificantly different baseline duration of the same group at P<0.05; ^bsignificantly different from AlCl₃ after 4 weeks induction at P<0.05; ^csignificantly different from baseline of the same group at P<0.05; ^dsignificantly different from AD group at P<0.05; ^esignificantly different from rivastigmine when each is used for 4 weeks in combination with AlCl₃ at P<0.05; ^fsignificantly different from same group when given alone for 4 weeks at P<0.05.
Abbreviation: AD, Alzheimer’s disease.

Biochemical parameters

Figure 8 shows the significant diminution in the Ach levels and also confirms the augmented level of AchE in the brain of the rats treated with the AlCl₃ compared with the normal control group rats. The AlCl₃-treated rats that received baicalein showed a significant improvement in the level of Ach, and reduction in the level of AchE, in a dose-dependent manner. However, rivastigmine showed a remarkable enhancement in the level of Ach, and reduction in the level of AchE, compared with the AD control group rats.

Figure 8 Protective effects of baicalein and rivastigmine on brain levels of (A) acetylcholine and (B) acetylcholinesterase in AD-induced rats.

Notes: All data are expressed as mean ± SE. ^#P<0.05 compared with the control group; *P<0.05, **P<0.01, and ***P<0.001 compared with the AD control group rats.
Abbreviations: AD, Alzheimer’s disease; SE, standard error.

Estimation of protein expression

Figure 9 represents the effect of protein expression with different proteins – namely, Aβ1–42, APP, β and γ secretases. We analyzed the effect of baicalein on the β-amyloid metabolic marker in the AD-induced rats.

Figure 9 The expression of APP, β-secretases, γ-secretases, β-actin, and Aβ1–42 compared to control.

Notes: Groups: A: Normal; B: AD; C: AD + baicalein (5 mg/kg); D: AD + baicalein (10 mg/kg); and E: AD + rivastigmine (0.3 mg/kg).
Abbreviations: AD, Alzheimer’s disease; APP, amyloid precursor protein.

Histopathological results for the protective and therapeutic groups

Figure 10 shows the highly active nerve cells along with the huge nuclei in the negative control group rats. However, the AD control group rats showed a spongy appearance, brain necrosis, loss of structure, plaques, nuclei of cells, and outlines. Some of the nuclei showed a ring appearance. AD group rats treated with baicalein and rivastigmine showed an improvement in histopathological changes compared with the AD control.

Figure 10 (A) Image of the brain section of a control rat showing normal histological structure of the hippocampus. (B) Image of the brain section of an Alzheimer’s disease-induced rat’s plaques formation. (C) AD group treated with baicalein (5 mg/kg). (D) AD group treated with baicalein (10 mg/kg). (E) AD group treated with rivastigmine (0.3 mg/kg). The tangle appears as a long pink filament in the cytoplasm (hematoxylin and eosin, 10×).

Abbreviation: AD, Alzheimer’s disease.

Discussion

AD is considered to be a neurodegenerative disorder differentiated by progressive degeneration of the cortical neurons and hippocampal cells, which negatively affects the cognitive ability and memory function. AD is commonly considered to be a precursor dementia. AD complications increase with age-related changes. A decline in short-term memory is commonly considered to be the first clinical sign of AD; thus, the level of cognitive ability, along with the capacity to use common tools and objects, is used to estimate the progression of short-term memory.^7,8 Anders and Martin reported that 35.6 million people have dementia worldwide, and this figure is predicted to rise to 65.7–115.4 million people from 2013 to 2050. AD affects individuals of both low- and middle-income groups. Several other factors – such as deficiency of Ach, the development of atherosclerotic lesions, oxidative stress, and inflammation of the brain – also play an important role in the progression of AD.

Aluminum is commonly found in soil, water, toothpaste, and food supplements, and is also used to make cooking implements. Several reports have revealed that aluminum causes the generation of free radicals in the brain and induces neurotoxicity. The deposition of free radicals in the brain may induce the degenerative events associated with aging, including AD. In the current investigation, the AD rat groups treated with AlCl₃ showed a reduction in cage activity and a reduced duration of rotation in the rotarod test, along with an increase in the time taken for the rats to reach the food in the T-maze test.^9,10 An increased level of AchE, but a reduced level of Ach, was found in the disease control group rats compared with the levels found in the normal control group rats. Mayeux and Sano showed that rivastigmine is the approved drug for the treatment of AD.¹¹ It is possible that the effect of the rivastigmine on AD was to improve the endogenous antioxidant mechanism and the level of oxidative stress, as revealed by the improvement in cage activity; it also altered the level of Ach and AchE in the brain compared with the levels in the AD control group rats. Onor et al reported that rivastigmine enhanced both the daily living activity, and cognitive and global functions.¹²

The Food and Drug Administration has approved the use of AchE inhibitors to treat AD. In the current investigation, we attempted to discover a potential new drug that could be used to prevent or slow down the disease process. Therefore, it is vital to develop herb- and medicinal plant-based drug therapies to prevent the development of neurodegenerative disorders, particularly those associated with memory dysfunction. In the current investigation, we explored the therapeutic and protective effect of baicalein vs rivastigmine in AD by assessing the effect of these drugs on the behavioral activity of rats.^9,10

In the current investigation, we used AlCl₃ to induce AD, as revealed by a weakening in the physical state of the rats during the cage activity test, deterioration in cognitive capacity during the T-maze test, and deterioration in motor coordination during the rotarod test. It also reduced the level of Ach, and enhanced the level of AchE, in the brain homogenates of the rats. This particular effect was confirmed via a histopathological study of the rats, which revealed the existence of amyloid plaques. The AD control group rats treated with baicalein and rivastigmine confirm the therapeutic and protective effects of baicalein and rivastigmine, as shown by the improvement of behavioral status revealed by the physical state activity, time duration of motor coordination, and altered levels of activity associated with changes in Ach and AchE levels. This result has been further confirmed by a histopathological study that showed the disappearance of the amyloid plaques, which were induced by AlCl₃.^13,14 Xiao et al and Shah and Reichman showed the possible mechanism of action of rivastigmine to be acting on the glutamate mechanisms, thereby reducing the oxidative stress and improving the endogenous antioxidant defense to protect against the Aβ-induced oxidative stress.^15,16

Conclusion

In the current investigation, baicalein was shown to have a therapeutic and protective effect on the AD-induced rats. These results could be of great significance in eliminating the neurodegenerative signs of AD. Maximum effect was revealed by higher doses of baicalein. The data suggest that baicalein offers a protective and therapeutic effect against the progressive neurological injury associated with AD, particularly in relation to oxidative stress. Further clinical and molecular research is required to determine the true efficacy of baicalein on neurodegenerative disorders.

Acknowledgments

This study was supported by the Natural Science Foundation of China (number 81271328) and the Science and Technology Projects Foundation of Guangzhou City (number 2014Y2-00501).

Disclosure

The authors report no conflicts of interest in this work.