Hosni Ahmed A, Abdel-Moneim A Adel, Abdel-Reheim Eman S, Mohamed Samah M, Helmy Hamdi
Molecular Physiology Division, Zoology Department, Faculty of Science, Beni-Suef University, 62511 Beni-Suef, Egypt.
Molecular Physiology Division, Zoology Department, Faculty of Science, Beni-Suef University, 62511 Beni-Suef, Egypt.
Biomed Pharmacother. 2017 Apr;88:52-60. doi: 10.1016/j.biopha.2017.01.054. Epub 2017 Jan 13.
Cinnamon has a history of use for medicinal purposes and its major benefits have been linked to cinnamaldehyde. The present study aimed to investigate the hypoglycemic action of cinnamaldehyde against fatty-sucrosed diet/streptozotocin (FSD/STZ)-rat model of gestational diabetes. Female albino rats were divided into three groups. Group I fed with normal diet (ND) while group II and III were fed with FSD for eight weeks (five weeks pre-gestational and three weeks gestational). Rats of group III were administered with a daily oral dose of 20mg/kg cinnamaldehyde one week before mating onward. At the 7th day of gestation, FSD-fed rats were injected intraperitoneally with STZ (25mg/kg b.wt.) to induce gestational diabetes. Pre-mating treatment of cinnamaldehyde controls hyperphagia and glucose intolerance during the gestational period than in diabetic rats. It also reduced levels of fructosamine, total cholesterols, triglycerides, leptin, tumor necrosis factor-alpha (TNF-α), malondialdehyde (MDA) and nitric oxide (NO), while it significantly increased levels of high-density lipoprotein (HDL)-cholesterol, adiponectin, liver glycogen, reduced glutathione (GSH) and catalase activity at term pregnancy. In addition, cinnamaldehyde administration up-regulated the mRNA expression of peroxisome proliferated activated receptor-gamma (PPARγ) and also ameliorated the number of viable fetuses, implantation loss sites, fetal glucose and insulin levels. In conclusion, cinnamaldehyde has safe hypoglycemic action on gestational diabetes by potentiating insulin secretion and sensitivity through activating the antioxidant defense system, suppressing pro-inflammatory cytokines production, upregulating PPARγ gene expression and alleviating the reproductive performance.
肉桂有着药用历史,其主要益处与肉桂醛有关。本研究旨在探讨肉桂醛对高脂蔗糖饮食/链脲佐菌素(FSD/STZ)诱导的妊娠糖尿病大鼠模型的降血糖作用。将雌性白化大鼠分为三组。第一组喂以正常饮食(ND),而第二组和第三组喂以高脂蔗糖饮食八周(妊娠前五周和妊娠三周)。第三组大鼠在交配前一周开始每日口服20mg/kg肉桂醛。在妊娠第7天,给喂高脂蔗糖饮食的大鼠腹腔注射链脲佐菌素(25mg/kg体重)以诱导妊娠糖尿病。与糖尿病大鼠相比,肉桂醛在交配前的治疗可控制妊娠期的食欲亢进和葡萄糖不耐受。它还降低了果糖胺、总胆固醇、甘油三酯、瘦素、肿瘤坏死因子-α(TNF-α)、丙二醛(MDA)和一氧化氮(NO)的水平,而在足月妊娠时显著提高了高密度脂蛋白(HDL)胆固醇、脂联素、肝糖原、还原型谷胱甘肽(GSH)和过氧化氢酶活性。此外,给予肉桂醛上调了过氧化物酶体增殖物激活受体-γ(PPARγ)的mRNA表达,还改善了活胎数量、着床丢失部位、胎儿葡萄糖和胰岛素水平。总之,肉桂醛通过激活抗氧化防御系统、抑制促炎细胞因子产生、上调PPARγ基因表达和改善生殖性能来增强胰岛素分泌和敏感性,从而对妊娠糖尿病具有安全的降血糖作用。