Raval Keval Y, Tirgar Pravin R
School of Pharmacy, R K University, Rajkot, Gujarat India.
J Diabetes Metab Disord. 2022 Dec 31;22(1):571-580. doi: 10.1007/s40200-022-01177-y. eCollection 2023 Jun.
The study was undertaken to evaluate the anti-diabetic potential of propoxybenzoic acid (PBA).
36 Sprague-Dawley rats of either sex were utilized for the study. Animals were injected with nicotinamide (230 mg/kg) followed by streptozotocin (65 mg/kg) to induce Type-2 Diabetes (T2DM). Animals with blood glucose levels (BGL) over 200 mg/kg were allocated in six groups. Three groups were treated with -PBA dose of 100 mg/kg, 200 mg/kg and 300 mg/kg respectively; standard control group was treated with 5 mg/kg glibenclamide, while the other two groups were considered as normal control and disease control group. Body weight (BW) and BGL were recorded on Day 0, Day 7, Day 14, and Day 28. Glycosylated hemoglobin (HbA1c), serum insulin levels and lipid profile were recorded on Day 28. Animals were euthanized on Day 28 and the pancreas was isolated for histopathological examination.
Diabetic animals treated with PBA showed significant improvements in BW ( < 0.05) and BGL ( < 0.001) over 28 days. Levels of HbA1c ( < 0.05) and serum insulin ( < 0.001) were significantly regulated in animals treated with PBA. A significant decrease ( < 0.001) was observed in elevated levels of TC, TG, LDL cholesterol and VLDL cholesterol in animals treated with PBA. -PBA significantly regulated the levels of HDL cholesterol ( < 0.001). A notable protective effect of PBA was observed through the histopathological examination of pancreas.
PBA can be characterized as a multi-target inhibiting anti-diabetic agent which can be evaluated against diabetic complications.
The online version contains supplementary material available at 10.1007/s40200-022-01177-y.
本研究旨在评估丙氧基苯甲酸(PBA)的抗糖尿病潜力。
选用36只成年Sprague-Dawley大鼠(雌雄不限)进行本研究。动物先注射烟酰胺(230mg/kg),随后注射链脲佐菌素(65mg/kg)以诱导2型糖尿病(T2DM)。血糖水平(BGL)超过200mg/kg的动物被分为六组。三组分别接受100mg/kg、200mg/kg和300mg/kg剂量的PBA治疗;标准对照组接受5mg/kg格列本脲治疗,另外两组分别作为正常对照组和疾病对照组。在第0天、第7天、第14天和第28天记录体重(BW)和BGL。在第28天记录糖化血红蛋白(HbA1c)、血清胰岛素水平和血脂谱。在第28天对动物实施安乐死,并分离胰腺进行组织病理学检查。
用PBA治疗的糖尿病动物在28天内体重(P<0.05)和BGL(P<0.001)有显著改善。用PBA治疗的动物中,HbA1c水平(P<0.05)和血清胰岛素水平(P<0.001)得到显著调节。用PBA治疗的动物中,升高的总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL胆固醇)和极低密度脂蛋白胆固醇水平显著降低(P<0.001)。PBA显著调节高密度脂蛋白胆固醇水平(P<0.001)。通过胰腺组织病理学检查观察到PBA有显著的保护作用。
PBA可被表征为一种多靶点抑制抗糖尿病药物,可用于评估糖尿病并发症。
在线版本包含可在10.1007/s40200-022-01177-y获取的补充材料。