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块茎甲醇提取物在小鼠疼痛模型中的抗伤害感受活性:α-肾上腺素能受体和钾通道的可能参与

Antinociceptive activity of methanol extract of tubers in murine model of pain: Possible involvement of α-adrenergic receptor and K channels.

作者信息

Abubakar Abdulhakim, Nazifi Abdullahi Balarabe, Odoma Saidi, Shehu Salisu, Danjuma Nuhu Mohammed

机构信息

Department of Pharmacology and Therapeutics, Ahmadu Bello University, Zaria, Nigeria.

Department of Pharmacology and Therapeutics, Bayero University, Kano, Nigeria.

出版信息

J Tradit Complement Med. 2019 Mar 16;10(1):1-6. doi: 10.1016/j.jtcme.2019.03.005. eCollection 2020 Jan.

Abstract

The tubers of are used in Nigerian Herbal Medicine for the management of diabetes mellitus, painful and inflammatory conditions. The antinociceptive activity has been validated but the mechanism of this activity is yet to be explored. This study therefore, aimed to investigate the probable mechanism(s) of the antinociceptive activity of tubers using experimental animal model of pain. HPLC and GC-MS analyses were carried out on the extract. Antinociceptive activity was investigated using acetic acid-induced writhing response test in mice. Three groups of mice were orally administered distilled water (10 ml/kg), (400 mg/kg) and morphine (10 mg/kg) 60 min before administration of acetic acid and the resulting writhing were counted for 10 min. To establish the probable mechanism(s) of action of , separate groups of animals were pretreated intraperitoneally with naloxone (2 mg/kg), prazosin (1 mg/kg), yohimbine (1 mg/kg), propranolol (20 mg/kg) and glibenclamide (5 mg/kg) 15 min before administration. HPLC chromatogram of the extract revealed seventeen characteristic peaks with retention times ranging between 2.1 and 7.4 min. Administration of significantly ( < 0.01) reduced the mean number of writhes compared to control group. Pretreatment with yohimbine and glibenclamide significantly ( < 0.05 and  < 0.01 respectively) reduced the antinociceptive activity of extract-alone treated group. However, pretreatment with prazosin, naloxone and propranolol showed no effect on its analgesic activity. The findings from this research revealed the possible involvement of α-adrenergic receptor and K channels in the antinociceptive activity of tuber extract.

摘要

[植物名称]的块茎在尼日利亚草药医学中用于治疗糖尿病、疼痛和炎症性疾病。其抗伤害感受活性已得到验证,但该活性的机制尚未探索。因此,本研究旨在使用疼痛实验动物模型研究[植物名称]块茎抗伤害感受活性的可能机制。对提取物进行了高效液相色谱(HPLC)和气相色谱 - 质谱联用(GC - MS)分析。使用小鼠醋酸诱导扭体反应试验研究抗伤害感受活性。在给予醋酸前60分钟,三组小鼠分别口服蒸馏水(10 ml/kg)、[植物名称提取物](400 mg/kg)和吗啡(10 mg/kg),并记录随后10分钟内的扭体次数。为确定[植物名称提取物]的可能作用机制,在给予[植物名称提取物]前15分钟,对不同组动物分别腹腔注射纳洛酮(2 mg/kg)、哌唑嗪(1 mg/kg)、育亨宾(1 mg/kg)、普萘洛尔(20 mg/kg)和格列本脲(5 mg/kg)。提取物的HPLC色谱图显示有17个特征峰,保留时间在2.1至7.4分钟之间。与对照组相比,给予[植物名称提取物]显著(P < 0.01)减少了平均扭体次数。用育亨宾和格列本脲预处理分别显著(P < 0.05和P < 0.01)降低了单独提取物处理组的抗伤害感受活性。然而,用哌唑嗪、纳洛酮和普萘洛尔预处理对其镇痛活性无影响。本研究结果表明α - 肾上腺素能受体和钾通道可能参与了[植物名称]块茎提取物的抗伤害感受活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5143/6957804/24ec619afe57/fx1.jpg

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