Bhatt Parloop, Makwana Dharmesh, Santani Devdas, Goyal Ramesh
Department of Pharmacology, L.M. College of Pharmacy, Navarangpura, Ahmedabad-380009, Gujarat, India.
Can J Physiol Pharmacol. 2007 May;85(5):514-20. doi: 10.1139/y07-031.
The present study was undertaken to investigate the effectiveness of adrenergic antagonists carvedilol and propranolol on L-thyroxin-induced cardiovascular and metabolic disturbances in rats. Treatment with L-thyroxin sodium (75 mg/kg body mass, s.c., every alternate day for 3 weeks), produced a significant increase in food and water intake, body temperature, heart rate, systolic blood pressure, along with an increase in serum T3, T4, and triglyceride levels. Besides a significant reduction in body mass, serum levels of TSH and cholesterol were also reduced following L-thyroxin treatment. Carvedilol (10 mg/kg body mass, orally) and propranolol (10 mg/kg body mass, i.p.) administered daily in the third week to 2 separate groups of L-thyroxin-treated animals reversed thyroxin-induced loss in body mass and rise in body temperature, blood pressure, and heart rate. Propranolol treatment increased TSH levels and decreased T3 and T4 levels in hyperthyroid animals, whereas carvedilol did not produce any effect on thyroid hormones. Carvedilol treatment reversed thyroxin induced hypertriglyceridemia, whereas propranolol treatment had no effect. Both carvedilol and propranolol prevented decrease in cholesterol levels induced by thyroxine. Compared with normal animals, L-thyroxin-treated animals showed a state of hyperglycemia, hyperinsulinaemia, impaired glucose tolerance, and insulin resistance, as inferred from elevated fasting serum glucose and insulin levels, higher area under the curve over 120 min for glucose, and decreased insulin sensitivity index (KITT). Propranolol and carvedilol treatment significantly decreased fasting serum glucose levels. Treatment with propranolol did not alter serum insulin levels, area-under-the-curve glucose, or KITT values. However, treatment with carvedilol significantly reduced area-under-the-curve glucose, decreased fasting serum insulin levels and significantly increased KITT values. In conclusion, carvedilol appears to produce favorable effects on insulin sensitivity and glycemic control and can therefore be considered as more efficacious adjunctive treatment than propranolol in hyperthyroidism.
本研究旨在探讨肾上腺素能拮抗剂卡维地洛和普萘洛尔对L-甲状腺素诱导的大鼠心血管和代谢紊乱的有效性。用L-甲状腺素钠(75mg/kg体重,皮下注射,隔天一次,共3周)治疗后,大鼠的食物和水摄入量、体温、心率、收缩压显著增加,同时血清T3、T4和甘油三酯水平升高。除体重显著降低外,L-甲状腺素治疗后血清TSH水平和胆固醇水平也降低。在第三周,分别对两组L-甲状腺素治疗的动物每日口服卡维地洛(10mg/kg体重)和腹腔注射普萘洛尔(10mg/kg体重),可逆转甲状腺素引起的体重减轻以及体温、血压和心率升高。普萘洛尔治疗可使甲状腺功能亢进动物的TSH水平升高,T3和T4水平降低,而卡维地洛对甲状腺激素无任何影响。卡维地洛治疗可逆转甲状腺素诱导的高甘油三酯血症,而普萘洛尔治疗无效。卡维地洛和普萘洛尔均可防止甲状腺素引起的胆固醇水平降低。与正常动物相比,L-甲状腺素治疗的动物表现出高血糖、高胰岛素血症、葡萄糖耐量受损和胰岛素抵抗状态, 这可通过空腹血清葡萄糖和胰岛素水平升高、葡萄糖120分钟曲线下面积增加以及胰岛素敏感性指数(KITT)降低来推断。普萘洛尔和卡维地洛治疗可显著降低空腹血清葡萄糖水平。普萘洛尔治疗未改变血清胰岛素水平、葡萄糖曲线下面积或KITT值。然而,卡维地洛治疗可显著降低葡萄糖曲线下面积,降低空腹血清胰岛素水平,并显著提高KITT值。总之,卡维地洛似乎对胰岛素敏感性和血糖控制产生有益影响,因此在甲状腺功能亢进症中可被认为是比普萘洛尔更有效的辅助治疗药物。