自发性糖尿病小鼠的收缩反应

Noriyasu Kanie, Katsuo Kamata
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引用次数: 39

摘要

本研究探讨超氧阴离子对自发性糖尿病小鼠去甲肾上腺素(NE)诱导的收缩反应的影响。在内皮完整的主动脉环中,NE仅引起非糖尿病小鼠的张力轻微增加(db/+M),但在自发性糖尿病小鼠中引起更大的剂量依赖性收缩(db/db小鼠)。SOD (180 U/ml)预处理可显著降低ne诱导的糖尿病小鼠的收缩反应,而对照组小鼠则无此作用。用Cu/Zn SOD抑制剂二乙基二硫代氨基甲酸(DETCA, 10−3 M)预处理后,ne诱导的收缩在对照组小鼠中显著增强,但在糖尿病小鼠中无明显作用。在糖尿病小鼠中,乙酰胆碱诱导的松弛的剂量-反应曲线略有减弱,但明显减弱。对照小鼠主动脉环与次黄嘌呤(10 ~ 5 M)、黄嘌呤氧化酶(0.1 U/ml)和过氧化氢酶(1000 U/ml)的混合物孵育后逐渐收缩。SOD (180 U/ml)或吲哚美辛(10 - 5 M)预处理或去除内皮细胞可消除这种收缩。吲哚美辛可明显减弱ne诱导的糖尿病小鼠的剂量依赖性收缩。这些结果表明,在db/db糖尿病小鼠中,超氧阴离子可能通过血管收缩剂前列腺素增强NE诱导的收缩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contractile responses in spontaneously diabetic mice

This study investigated the influence of superoxide anion on the norepinephrine (NE)-induced contractile response in spontaneously diabetic mice. In aortic rings with intact endothelium, NE elicited only a slight increase in tension in nondiabetic mice (db/+M), but a much greater dose-dependent contraction in spontaneously diabetic mice (db/db mice). The NE-induced contractile response was significantly reduced by pretreatment with SOD (180 U/ml) in diabetic mice, but not in control mice. The NE-induced contraction was significantly enhanced by pretreatment with diethyldithiocarbamic acid (DETCA, 10−3 M), a Cu/Zn SOD inhibitor, in control mice, but not in diabetic mice. The dose–response curve for the acetylcholine-induced relaxation was slightly, but significantly attenuated in diabetic mice. When aortic rings from control mice were incubated with a mixture of hypoxanthine (10−5 M), xanthine oxidase (0.1 U/ml) and catalase (1000 U/ml) in control mice, they gradually contracted. This contraction was abolished by pretreatment with SOD (180 U/ml) or indomethacin (10−5 M) or by removal of the endothelium. The enhanced NE-induced dose-dependent contraction seen in diabetic mice was markedly attenuated by indomethacin. These results suggest that in db/db diabetic mice, superoxide anion, perhaps via vasoconstrictor prostanoids, may enhance the contraction induced by NE.

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