Neuropharmacological potentials (antipsychotic-, anxiolytic-, and antidepressant-like activity) of Methanol Leaf Extract of Andrographis paniculata Nees in vivo: Possible mechanisms, antioxidant activity, and in silico supportive evidence.

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL
Memshima M Terhemen, Elohor Okpakpor, Oluwole Akawa, Israel O Bolanle, Raymond I Ozolua
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引用次数: 0

Abstract

Ethnopharmacology relevance: In Asia and parts of Africa, extracts from Andrographis paniculata Nees (Acanthaceae) are used as traditional remedies for a number of ailments such as tuberculosis, sinusitis, syphilis, leprosy, diarrhea, and malaria. There has been extensive research detailing the various pharmacological actions of Andrographis paniculata Nees (Acanthaceae). However, there is a paucity of scientific information on its neuropharmacological potential despite its traditional use to manage depression and anxiety in West Africa.

Aim of study: This study aims to evaluate the neuropharmacological activities of Andrographis paniculata Nees (Acanthaceae) in mice.

Methods: Acute oral toxicity was evaluated on the methanol extract of Andrographis paniculata (MEAP) before screening it for neuropsychopharmacological properties including antipsychotic-like, anxiolytic-like, antidepressant-like, sedative-hypnotic, anticonvulsant, and motor coordination after administering it for 10 consecutive days using oral doses of 100, 200, 400 mg/kg. The principal constituent andrographolide was evaluated for antipsychotic-like property over a range of doses (2-32 mg/kg). The brains of MEAP-treated mice were assayed for antioxidant enzymes and lipid peroxidation. Molecular docking was used to evaluate the degree of binding of andrographolide to 5-HT2A and D2 receptors.

Results: MEAP is relatively safe with oral LD50 >5000 mg/kg. It significantly dose- and time-dependently attenuated amphetamine- and ketamine-induced psychosis-like behavior. The effect of andrographolide on amphetamine-induced psychosis-like behavior was significant only at 8 mg/kg dose. MEAP showed anxiolytic-like and antidepressant-like properties but did not enhance phenobarbitone-induced sleep. It did not protect the mice against chemically induced convulsions and did not affect the motor-coordinating ability of mice. MEAP significantly increased the brain levels of superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, and reduced the levels of malondialdehyde. Andrographolide bound to D2 and 5-HT2A receptors but less than risperidone and aripiprazole at D2 and 5-HT2A, respectively.

Conclusion: The methanol extract of Andrographis paniculata possesses antipsychotic-like property possibly mediated by one or more of its constituents rather than solely by andrographolide. It also possesses anxiolytic- and antidepressant-like actions. The brain antioxidant property of the extract complements its neuropsychopharmacological actions.

穿心莲甲醇叶提取物在体内的神经药理学潜力(抗精神病、抗焦虑和抗抑郁活性):可能的机制、抗氧化活性和硅支持证据。
民族药理学相关性:在亚洲和非洲部分地区,穿心莲(穿心莲科)的提取物被用作治疗许多疾病的传统药物,如肺结核、鼻窦炎、梅毒、麻风病、腹泻和疟疾。有广泛的研究详细介绍穿心莲的各种药理作用(穿心莲科)。然而,尽管它在西非传统上用于治疗抑郁和焦虑,但关于其神经药理潜力的科学信息仍然缺乏。研究目的:研究穿心莲对小鼠的神经药理作用。方法:对穿心术甲醇提取物(MEAP)进行急性口服毒性评价,以100、200、400 mg/kg的口服剂量连续给药10 d,筛选其神经精神药理学特性,包括抗精神病样、抗焦虑样、抗抑郁样、镇静催眠、抗惊厥、运动协调等。主要成分穿心莲内酯在一定剂量范围内(2- 32mg /kg)评估抗精神病药物样性质。对meap处理小鼠的大脑进行抗氧化酶和脂质过氧化测定。通过分子对接评价穿心莲内酯与5-HT2A和D2受体的结合程度。结果:MEAP在口服LD50 ~ 5000 mg/kg时相对安全。它显著地以剂量和时间依赖性减弱安非他明和氯胺酮引起的精神病样行为。穿心莲内酯仅在8 mg/kg剂量时对安非他明诱导的类精神病行为有显著影响。MEAP表现出抗焦虑和抗抑郁的特性,但没有增强苯巴比妥诱导的睡眠。它不能保护小鼠免受化学诱发的惊厥,也不会影响小鼠的运动协调能力。MEAP显著提高了大脑超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶的水平,并降低了丙二醛的水平。穿心莲内酯与D2和5-HT2A受体结合,但分别低于利培酮和阿立哌唑对D2和5-HT2A的结合。结论:穿心莲甲醇提取物具有类似抗精神病的作用,可能是由其一种或多种成分介导的,而不是由穿心莲内酯单独介导的。它还具有抗焦虑和抗抑郁的作用。提取物的脑抗氧化特性补充了其神经精神药理学作用。
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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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