Δ9-tetrahydrocannabinol治疗可改善链脲佐菌素/烟酰胺诱导的糖尿病大鼠主动脉内皮依赖性松弛。

A Altınok, Z M Coşkun, K Karaoğlu, S Bolkent, A G Akkan, Sibel Özyazgan
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引用次数: 4

摘要

目的:本研究探讨过氧化物酶体增殖物激活受体γ (PPARγ)激动剂Δ(9)-四氢大麻酚(THC)对链脲佐剂/烟酰胺(STZ/NIC)诱导的2型糖尿病代谢控制和血管并发症的可能影响。材料与方法:先给药65 mg/kg STZ诱导2型糖尿病,15 min后腹腔注射85 mg/kg NIC。糖尿病诱导后3 d,给予四氢大麻酚(3 mg/kg/d, ig),连续7 d。测定各组大鼠在糖尿病诱导前及诱导后3周末的体重和血糖水平。计算乙酰胆碱(Ach)和硝普钠(SNP)对去甲肾上腺素(NA)预收缩主动脉环的效价和最大舒张效应。结果:3周结束时,糖尿病组血糖水平较对照组明显升高。四氢大麻酚治疗显著降低了升高的血糖水平。在离体糖尿病大鼠主动脉上,乙酰胆碱诱导的舒张功能受损,而内皮不依赖于SNP的舒张功能不受影响。四氢大麻酚可增强乙酰胆碱诱导的糖尿病大鼠主动脉松弛。讨论:这些结果表明,四氢大麻酚改善了STZ/NIC诱导的糖尿病大鼠主动脉内皮依赖性松弛,这些作用至少部分是通过控制高血糖和提高内皮一氧化氮的生物利用度来介导的。
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Δ9-tetrahydrocannabinol treatment improved endothelium-dependent relaxation on streptozotocin/nicotinamide-induced diabetic rat aorta.

Objective: In this study, we investigated the possible effect of Δ(9)-tetrahydrocannabinol (THC), a peroxisome proliferator-activated receptor gamma (PPARγ) agonist, on metabolic control and vascular complications of diabetes in streptozotocin/nicotinamide (STZ/NIC) induced type 2 diabetes mellitus.

Material and methods: Type 2 diabetes was induced with 65 mg/kg STZ, 15 minute later 85 mg/kg NIC was given intraperitoneally (i.p.) to rats. Three days after diabetes induction, THC (3 mg/kg/day, i.p.) was given for 7 days to diabetic rats. Body weight and plasma glucose levels of rats were measured in all groups before and at the end of 3 weeks after diabetes induction. Acetylcholine (Ach) and sodium nitroprusside (SNP) potency and maximum relaxant effects were calculated on aortic rings pre-contracted with noradrenaline (NA).

Results: At the end of 3 weeks, blood glucose levels of diabetic group significantly increased in comparison with the control group. Increased plasma glucose levels were significantly decreased by the treatment of THC. Ach induced relaxation was impaired whereas endothelium-independent relaxation to SNP was unaffected on isolated diabetic rat aorta. THC treatment enhanced Ach induced relaxation on diabetic rat aortas.

Discussion: These results suggested that THC improved endothelium-dependent relaxation in STZ/NIC induced diabetic rat aorta and that these effects were mediated at least in part, by control of hyperglycemia and enhanced endothelial nitric oxide bioavailability.

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来源期刊
Acta physiologica Hungarica
Acta physiologica Hungarica 医学-生理学
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