1.Mechanism of Zhifuxin in prevention and treatment of vascular dementia in long-term hypoperfused rats.
Xiao-Qing LI ; Xue ZHOU ; Jiu-Qun ZHU ; Zheng-Huai TAN
China Journal of Chinese Materia Medica 2025;50(7):1900-1907
This paper aims to evaluate the pharmacodynamic effect and mechanism of Zhifuxin in the prevention and treatment of vascular dementia(VD), providing a theoretical basis for later development. Bilateral common carotid artery ligation in male Wistar rats was conducted to replicate the long-term hypoperfused VD model, and the drug was given to groups after one month. The rats were fed daily with nimodipine of 20 mg·kg~(-1), Zhifuxin of 50, 100, and 200 mg·kg~(-1), or the same volume of solvent for four weeks. 24 hours after the last dose, Morris water maze experiments were performed to detect the learning and memory abilities of rats. Hematoxylin-eosin(HE) staining was used to observe the pathological changes in the brain tissue of rats; the immunohistochemical method was used to detect the expression of muscarinic acetylcholine receptors M1 and M4 in rats and determine the content of acetyl choline(Ach), acetylcholin esterase(AchE), malondialdehyde(MDA), choline acetyl transferase(ChAT), and dimethyl arginine hydrolase 1(DDAH1) in the cerebral cortex of rats. Western blot was employed to detect protein expression of endothelial nitric oxide synthase(eNOS), caveolin-1, monoamine oxidase A(MAO-A), and monoamine oxidase B(MAO-B). RT-qPCR was utilized to detect mRNA expression of eNOS, caveolin-1, MAO-A, and MAO-B. The results showed that compared with the model group, the different doses of Zhifuxin were able to shorten the latency of VD rats in the water maze positioning navigation test, increase the number of crossing platforms in the space exploration test, and alleviate cone cell contracture in the hippocampus of VD rats. The expression of biochemical indicators related to the cholinergic system in the cerebral cortex: M1 and M4 receptors increased, as well as ChAT activity, and AchE activity significantly decreased. The protein and mRNA expression of indicators related to the eNOS/NO pathway: DDAH1 content, eNOS, and caveolin-1 increased, and that of indicators related to monoamine oxidase(MAO): MAO-A and MAO-B significantly decreased. The results show that Zhifuxin can improve cognition ability in long-term hypoperfused VD rats, and its mechanism of action may be related to its ability to modulate the cholinergic system and the eNOS/NO pathway and inhibit MAO expression.
Animals
;
Dementia, Vascular/metabolism*
;
Male
;
Rats, Wistar
;
Rats
;
Drugs, Chinese Herbal/administration & dosage*
;
Maze Learning/drug effects*
;
Nitric Oxide Synthase Type III/genetics*
;
Acetylcholinesterase/metabolism*
;
Humans
;
Choline O-Acetyltransferase/genetics*
;
Disease Models, Animal
2.A new benzaldehyde from the coral-derived fungus Aspergillus terreus C23-3 and its anti-inflammatory effects via suppression of MAPK signaling pathway in RAW264.7 cells.
Minqi CHEN ; Jinyue LIANG ; Yuan WANG ; Yayue LIU ; Chunxia ZHOU ; Pengzhi HONG ; Yi ZHANG ; Zhong-Ji QIAN
Journal of Zhejiang University. Science. B 2022;23(3):230-240
Marine fungi are important members of the marine microbiome, which have been paid growing attention by scientists in recent years. The secondary metabolites of marine fungi have been reported to contain rich and diverse compounds with novel structures (Chen et al., 2019). Aspergillus terreus, the higher level marine fungus of the Aspergillus genus (family of Trichocomaceae, order of Eurotiales, class of Eurotiomycetes, phylum of Ascomycota), is widely distributed in both sea and land. In our previous study, the coral-derived A. terreus strain C23-3 exhibited potential in producing other biologically active (with antioxidant, acetylcholinesterase inhibition, and anti-inflammatory activity) compounds like arylbutyrolactones, territrems, and isoflavones, and high sensitivity to the chemical regulation of secondary metabolism (Yang et al., 2019, 2020; Nie et al., 2020; Ma et al., 2021). Moreover, we have isolated two different benzaldehydes, including a benzaldehyde with a novel structure, from A. terreus C23-3 which was derived from Pectinia paeonia of Xuwen, Zhanjiang City, Guangdong Province, China.
Acetylcholinesterase/metabolism*
;
Animals
;
Anthozoa/microbiology*
;
Anti-Inflammatory Agents/pharmacology*
;
Aspergillus/chemistry*
;
Benzaldehydes/pharmacology*
;
Mice
;
RAW 264.7 Cells
;
Signal Transduction
3.Echinacoside Alleviates Cognitive Impairment in Cerebral Ischemia Rats through α 7nAChR-Induced Autophagy.
Ling DING ; Hong YE ; Long-Dian GU ; An-Qing DU ; Xin-Lu YUAN
Chinese journal of integrative medicine 2022;28(9):809-816
OBJECTIVES:
To evaluate the effect of echinacoside (ECH) on cognitive dysfunction in post cerebral stroke model rats.
METHODS:
The post stroke cognitive impairment rat model was created by occlusion of the transient middle cerebral artery (MCAO). The rats were randomly divided into 3 groups by a random number table: the sham group (sham operation), the MCAO group (received operation for focal cerebral ischemia), and the ECH group (received operation for focal cerebral ischemia and ECH 50 mg/kg per day), with 6 rats in each group. The infarct volume and spatial learning were evaluated by triphenyl tetrazolium chloride staining and Morris water maze. The expression of α7nAChR in the hippocampus was detected by immunohistochemistry. The contents of acetylcholine (ACh), malondialdehyde (MDA), glutathione (GSH), superoxide dismutase (SOD), activities of choline acetyltransferase (ChAT), acetylcholinesterase (AChE), and catalase (CAT) were evaluated by enzyme linked immunosorbent assay. The neural apoptosis and autophagy were determined by TUNEL staining and LC3 staining, respectively.
RESULTS:
ECH significantly lessened the brain infarct volume and ameliorated neurological deficit in infarct volume and water content (both P<0.01). Compared with MCAO rats, administration of ECH revealed shorter escape latency and long retention time at 7, 14 and 28 days (all P<0.01), increased the α7nAChR protein expression, ACh content, and ChAT activity, and decreased AChE activity in MCAO rats (all P<0.01). ECH significantly decreased MDA content and increased the GSH content, SOD, and CAT activities compared with MCAO rats (all P<0.05). ECH suppressed neuronal apoptosis by reducing TUNEL-positive cells and also enhanced autophagy in MCAO rats (all P<0.01).
CONCLUSION
ECH treatment helped improve cognitive impairment by attenuating neurological damage and enhancing autophagy in MCAO rats.
Acetylcholinesterase
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Animals
;
Autophagy
;
Brain Ischemia/metabolism*
;
Cerebral Infarction
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Cognitive Dysfunction/drug therapy*
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Glutathione/metabolism*
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Glycosides
;
Infarction, Middle Cerebral Artery/drug therapy*
;
Neuroprotective Agents/therapeutic use*
;
Rats
;
Rats, Sprague-Dawley
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Reperfusion Injury/drug therapy*
;
Stroke/drug therapy*
;
Superoxide Dismutase/metabolism*
;
alpha7 Nicotinic Acetylcholine Receptor
4.Diterpenoid alkaloids from roots of Aconitum kongboense.
Chao-Yin XIE ; Shuai HUANG ; Lin CHEN ; Feng GAO ; Xian-Li ZHOU
China Journal of Chinese Materia Medica 2021;46(17):4424-4432
The chemical constituents from the roots of Aconitum kongboense were studied. Twenty-five diterpenoid alkaloids were isolated from the 95% methanol extract of the roots of A. kongboense by silica gel, reverse-phase silica gel and basic alumina column chromatography. They included a new aconitine-type diterpenoid alkaloid, named as kongboensenine(1), and twenty-four known ones(2-25), i.e., acotarine F(2), acotarine G(3), 14-acetyltalatisamine(4), talatisamine(5), indaconitine(6), yunaconitine(7), chasmanine(8), 6-epi-foresticine(9), homochasmanine(10), 8-deacetyl-yunaconitine(11), chasmaconitine(12), ajaconine(13), franchetine(14), ezochasmanine(15), crassicautine(16), 14-O-deacylcrassicausine(17), genicunine A(18), falconeridine(19), sachaconitine(20), liljestrandisine(21), 8-methyl-14-acetyltalatisamine(22), kongboendine(23), 14-benzoylchasmanine(24) and pseudaconine(25). Their structures were elucidated by common spectroscopic methods including high-resolution electrospray ionization mass spectrometry(HR-ESI-MS) and nuclear magnetic resonance(NMR) techniques. Compounds 2-4, 10, 13, 15-19 and 21-22 were isolated from this plant for the first time. Experimental results showed that all compounds did not have a significant inhibitory activity against acetylcholinesterase(AChE).
Acetylcholinesterase
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Aconitum/metabolism*
;
Alkaloids
;
Diterpenes
;
Magnetic Resonance Spectroscopy
;
Molecular Structure
;
Plant Roots/metabolism*
5.Time-dependent Expression and Distribution of AChE during the Skin Incised Wound Healing in Mice.
Jian-xin ZHAO ; Xin JIN ; Jun-jie HUANG ; Yi YAO ; Lin-sheng YU ; Yan-yan FAN
Journal of Forensic Medicine 2019;35(2):143-148
Objective To study the time-dependent expression and distribution of acetylcholinesterase (AChE) during skin incised wound healing in mice, and discuss its effect in wound healing as well as the feasibility of using it as a reference index for wound age estimation. Methods A total of 45 C57BL/KsJ mice were randomly divided into one control group and eight incised groups. The skin incised wound model was established in the incised groups with samples of skin wounds taken at 6 h, 12 h, 1 d, 3 d, 5 d, 7 d, 10 d and 14 d post-injury respectively, while the uninjured skin tissue was extracted in the control group. Expression and distribution of AChE in skin samples were detected by immunohistochemistry, double immunofluorescence and Western blotting. Results Immunohistochemistry results indicated that AChE was mainly detected in infiltrating polymorphonuclear cells (PMNs) 6 to 12 h post-injury. A large number of AChE-positive mononuclear cells (MNCs) were observed 1 to 3 d post-injury. The AChE-positive cells were mainly fibroblastic cells (FBCs) 5 to 14 d post-injury. The ratio of the AChE-positive cells increased initially 6 h post-injury, and reached the peak at 1 d post-injury. Double immunofluorescent staining showed that the majority of AChE-positive MNCs and FBCs expressed macrophage marker and myofibroblast marker, respectively. Western blotting results showed that the relative expression level of AChE in the incised group was higher than that in the control group averagely, reached the peak at 1 d post-injury, then reached a second peak at 7 d post-injury. Conclusion The expression of AChE is found in PMNs, macrophages and myofibroblast during skin wound healing, which indicates it might be involved in the adjustment of inflammatory response and fibrotic repair after injury. Moreover, combined use of various methods for the detection of the expression of AChE would provide reference for skin wound age estimation.
Acetylcholinesterase/metabolism*
;
Animals
;
Mice
;
Mice, Inbred C57BL
;
Skin/pathology*
;
Time Factors
;
Wound Healing/physiology*
6.Isolation and identification of endophytic fungi from Huperzia serrata and their metabolites' inhibitory activities against acetylcholinesterase and anti-inflammatory activities.
Bo-Wen QI ; Ting MO ; Xin ZHANG ; Ya-Ru YAN ; Xi-Ping XU ; Hong-Yun YANG ; Xiao-Hui WANG ; Jun LI ; She-Po SHI ; Xiao LIU
China Journal of Chinese Materia Medica 2019;44(15):3213-3220
A total of 27 endophytic fungal strains were isolated from Huperzia serrata,which were richly distributed in the stems and leaves while less distributed in roots. The 27 strains were identified by Internal Transcribed Spacer( ITS) r DNA molecular method and one of the strains belongs to Basidiomycota phylum,and other 26 stains belong to 26 species,9 general,6 families,5 orders,3 classes of Ascomycota Phylum. The dominant strains were Colletotrichum genus,belonging to Glomerellaceae family,Glomerellales order,Sordariomycetes class,Ascomycota Phylum,with the percentage of 48. 15%. The inhibitory activities of the crude extracts of 27 endophytic fungal strains against acetylcholinesterase( ACh E) and nitric oxide( NO) production were evaluated by Ellman's method and Griess method,respectively. Crude extracts of four fungi exhibited inhibitory activities against ACh E with an IC50 value of 42. 5-62. 4 mg·L~(-1),and some fungi's crude extracts were found to inhibit nitric oxide( NO) production in lipopolysaccharide( LPS)-activated RAW264. 7 macrophage cells with an IC50 value of 2. 2-51. 3 mg·L~(-1),which indicated that these fungi had potential anti-inflammatory activities.The chemical composition of the Et OAc extract of endophytic fungus HS21 was also analyzed by LCMS-IT-TOF. Seventeen compounds including six polyketides,four diphenyl ether derivatives and seven meroterpenoids were putatively identified.
Acetylcholinesterase
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Animals
;
Anti-Inflammatory Agents
;
isolation & purification
;
pharmacology
;
Ascomycota
;
chemistry
;
classification
;
isolation & purification
;
Cholinesterase Inhibitors
;
isolation & purification
;
metabolism
;
Endophytes
;
classification
;
isolation & purification
;
Huperzia
;
microbiology
;
Mice
;
RAW 264.7 Cells
7.Atlas of the Striatum and Globus Pallidus in the Tree Shrew: Comparison with Rat and Mouse.
Rong-Jun NI ; Zhao-Huan HUANG ; Yu-Mian SHU ; Yu WANG ; Tao LI ; Jiang-Ning ZHOU
Neuroscience Bulletin 2018;34(3):405-418
The striatum and globus pallidus are principal nuclei of the basal ganglia. Nissl- and acetylcholinesterase-stained sections of the tree shrew brain showed the neuroanatomical features of the caudate nucleus (Cd), internal capsule (ic), putamen (Pu), accumbens, internal globus pallidus, and external globus pallidus. The ic separated the dorsal striatum into the Cd and Pu in the tree shrew, but not in rats and mice. In addition, computer-based 3D images allowed a better understanding of the position and orientation of these structures. These data provided a large-scale atlas of the striatum and globus pallidus in the coronal, sagittal, and horizontal planes, the first detailed distribution of parvalbumin-immunoreactive cells in the tree shrew, and the differences in morphological characteristics and density of parvalbumin-immunoreactive neurons between tree shrew and rat. Our findings support the tree shrew as a potential model for human striatal disorders.
Acetylcholinesterase
;
metabolism
;
Animals
;
Brain Mapping
;
Corpus Striatum
;
anatomy & histology
;
cytology
;
metabolism
;
Globus Pallidus
;
anatomy & histology
;
cytology
;
metabolism
;
Imaging, Three-Dimensional
;
Male
;
Mice
;
Mice, Inbred C57BL
;
Models, Neurological
;
Neurons
;
metabolism
;
Parvalbumins
;
metabolism
;
Rats
;
Rats, Sprague-Dawley
;
Statistics, Nonparametric
;
Tupaiidae
;
anatomy & histology
8.Neuroprotective effect of the ethanol extract of Artemisia capillaris on transient forebrain ischemia in mice via nicotinic cholinergic receptor.
Huiyoung KWON ; Ji Wook JUNG ; Young Choon LEE ; Jong Hoon RYU ; Dong Hyun KIM
Chinese Journal of Natural Medicines (English Ed.) 2018;16(6):428-435
Artemisia capillaris Thunberg is a medicinal plant used as a traditional medicine in many cultures. It is an effective remedy for liver problems including hepatitis. Recent pharmacological reports have indicated that Artemisia species can exert various neurological effects. Previously, we reported a memory-enhancing effect of Artemisia species. However, the mechanisms underlying the neuroprotective effect of A. capillaris (AC) are still unknown. In the present study, we investigated the effect of an ethanol extract of AC on ischemic brain injury in a mouse model of transient forebrain ischemia. The mice were treated with AC for seven days, beginning one day before induction of transient forebrain ischemia. Behavioral deficits were investigated using the Y-maze. Nissl and Fluoro-jade B staining were used to indicate the site of injury. To determine the underlying mechanisms for the drug, we measured acetylcholinesterase activity. AC (200 mg·kg) treatment reduced transient forebrain ischemia-induced neuronal cell death in the hippocampal CA1 region. The AC-treated group also showed significant amelioration in the spontaneous alternation of the Y-maze test performance, compared to that in the untreated transient forebrain ischemia group. Moreover, AC treatment showed a concentration-dependent inhibitory effect on acetylcholinesterase activity in vitro. Finally, the effect of AC on forebrain ischemia was blocked by mecamylamine, a nonselective nicotinic acetylcholine receptor antagonist. Our results suggested that in a model of forebrain ischemia, AC protected against neuronal death through the activation of nicotinic acetylcholine receptors.
Acetylcholinesterase
;
metabolism
;
Animals
;
Artemisia
;
Cell Death
;
drug effects
;
Cholinergic Antagonists
;
pharmacology
;
Disease Models, Animal
;
Ethanol
;
chemistry
;
Hippocampus
;
pathology
;
physiopathology
;
Ischemic Attack, Transient
;
drug therapy
;
pathology
;
physiopathology
;
Male
;
Mecamylamine
;
pharmacology
;
Memory
;
drug effects
;
Mice
;
Mice, Inbred C57BL
;
Models, Neurological
;
Neuroprotective Agents
;
administration & dosage
;
pharmacology
;
Phytotherapy
;
Plant Components, Aerial
;
chemistry
;
Plant Extracts
;
administration & dosage
;
pharmacology
;
Receptors, Cholinergic
;
metabolism
9.New diterpenoids isolated from Leonurus japonicus and their acetylcholinesterase inhibitory activity.
Han-Kui WU ; Ting SUN ; Feng ZHAO ; Li-Ping ZHANG ; Gang LI ; Jie ZHANG
Chinese Journal of Natural Medicines (English Ed.) 2017;15(11):860-864
Three new labdane diterpenoids, leojaponicone A (1), isoleojaponicone A (2) and methylisoleojaponicone A (3), were isolated from the herb of Leonurus japonicus. The chemical structures of these secondary metabolites were elucidated on the basis of 1D and 2D NMR, including HMQC, and HMBC spectroscopic techniques. All the new compounds were tested in vitro for their acetylcholinesterase and α-glucosidase inhibitory activity. Compounds 1-3 exhibited low inhibitory effects on α-glucosidase with respect to acarbose and exhibited high inhibitory effects on acetylcholinesterase with respect to huperzine A.
Acetylcholinesterase
;
metabolism
;
Cholinesterase Inhibitors
;
chemistry
;
isolation & purification
;
pharmacology
;
Diterpenes
;
chemistry
;
isolation & purification
;
pharmacology
;
Glycoside Hydrolase Inhibitors
;
chemistry
;
isolation & purification
;
pharmacology
;
Leonurus
;
chemistry
;
Magnetic Resonance Spectroscopy
;
Molecular Structure
;
Plant Extracts
;
chemistry
;
pharmacology
10.Protective effect of capsaicin against methyl methanesulphonate induced toxicity in the third instar larvae of transgenic Drosophila melanogaster (hsp70-lacZ)Bg.
Saba KHANAM ; Ambreen FATIMA ; Rahul Smita JYOTI ; Fahad ALI ; Falaq NAZ ; Barkha SHAKYA ; Yasir Hasan SIDDIQUE
Chinese Journal of Natural Medicines (English Ed.) 2017;15(4):271-280
Capsaicin (trans-8-methyl-N-vanillyl-6-nonenamide) is the main component in hot peppers, including red chili peppers, jalapenos, and habanero, belonging to the genus Capsicum. Capsaicin is a potent antioxidant that interferes with free radical activities. In the present study, the possible protective effect of capsaicin was studied against methyl methanesulphonate (MMS) induced toxicity in third instar larvae of transgenic Drosophila melanogaster (hsp70-lacZ)Bg. The third instar was allowed to feed on the diet having different doses of capsaicin and MMS separately and in combination. The results suggested that the exposure of third instar larvae to the diet having MMS alone showed significant hsp70 expression as well as tissue DNA and oxidative damage, whereas the larvae feed on the diet having MMS and capsaicin showed a decrease in the toxic effects for 48-h of exposure. In conclusion, capsaicin showed a dose-dependent decrease in the toxic effects induced by MMS in the third instar larvae of transgenic Drosophila melanogaster.
Acetylcholinesterase
;
metabolism
;
Animals
;
Animals, Genetically Modified
;
Anticarcinogenic Agents
;
pharmacology
;
Capsaicin
;
pharmacology
;
DNA Damage
;
drug effects
;
Drosophila melanogaster
;
drug effects
;
Larva
;
drug effects
;
Methyl Methanesulfonate
;
antagonists & inhibitors

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