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卡西酮:一种(阿拉伯茶)生物碱加剧了糖尿病诱导大鼠的高血糖症。

Cathinone: An alkaloid of (Khat) exacerbated hyperglycemia in diabetes-induced rats.

作者信息

Alsalahi Abdulsamad, Chik Zamri, Mohamed Zahurin, Giribabu Nelli, Alshawsh Mohammed Abdullah

机构信息

Department of Pharmacology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.

Department of Pharmacology, Faculty of Pharmacy, Sana'a University, Mazbah District, 1247 Sana'a Secretariat, Yemen.

出版信息

Saudi J Biol Sci. 2021 Aug;28(8):4633-4643. doi: 10.1016/j.sjbs.2021.04.072. Epub 2021 May 1.

Abstract

Cathinone, the main bioactive alkaloid of (khat), slightly increased the blood sugar levels of healthy animals, while its effect on blood sugar levels of diabetic animals has not yet been reported. This study investigated the inhibition of cathinone on α-amylase and α-glucosidase as well as its glycemic effects in diabetes-induced rats. Rats were fed on a high fat diet for five weeks, which then intraperitoneally injected with streptozotocin (30 mg/kg). Diabetic rats were distributed randomly into diabetic control (DC, n = 5), 10 mg/kg glibenclamide-treated group (DG, n = 5), and 1.6 mg/kg cathinone-treated group (CAD, n = 5). Additional healthy untreated rats (n = 5) served as a nondiabetic negative control group. Throughout the experiment, fasting blood sugar (FBS), caloric intake and body weight were recorded weekly. By the 28th day of treatment, rats were euthanized to obtain blood samples and pancreases. The results demonstrated that cathinone exerted a significantly less potent inhibition than α-acarbose against α-amylase and α-glucosidase. As compared to diabetic control group, cathinone significantly increased FBS of diabetic rats, while insulin levels of diabetic rats significantly decreased. In conclusion, cathinone was unable to induce a substantial inhibition on α-amylase and α-glucosidase, while it exacerbated the hyperglycemia of diabetes-induced rats.

摘要

卡西酮是巧茶的主要生物活性生物碱,它会使健康动物的血糖水平略有升高,而其对糖尿病动物血糖水平的影响尚未见报道。本研究调查了卡西酮对α-淀粉酶和α-葡萄糖苷酶的抑制作用及其对糖尿病诱导大鼠的血糖影响。大鼠连续五周喂食高脂饮食,然后腹腔注射链脲佐菌素(30mg/kg)。将糖尿病大鼠随机分为糖尿病对照组(DC,n = 5)、10mg/kg格列本脲治疗组(DG,n = 5)和1.6mg/kg卡西酮治疗组(CAD,n = 5)。另外5只未治疗的健康大鼠作为非糖尿病阴性对照组。在整个实验过程中,每周记录空腹血糖(FBS)、热量摄入和体重。在治疗的第28天,对大鼠实施安乐死以获取血样和胰腺。结果表明,与阿卡波糖相比,卡西酮对α-淀粉酶和α-葡萄糖苷酶的抑制作用明显较弱。与糖尿病对照组相比,卡西酮显著提高了糖尿病大鼠的FBS,而糖尿病大鼠的胰岛素水平显著降低。总之,卡西酮对α-淀粉酶和α-葡萄糖苷酶无法产生实质性抑制作用,同时它加剧了糖尿病诱导大鼠的高血糖症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/635d/8325054/f87fa64c4930/gr1.jpg

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