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链脲佐菌素诱导的糖尿病大鼠中血小板活化因子和乙酰胆碱所致降压反应的减弱

Attenuation of depressor response induced by platelet activating factor and acetylcholine in streptozotocin-induced diabetic rats.

作者信息

Abiru T, Kamata K, Kasuya Y

机构信息

Biology Laboratory, Yamasa Shoyu Co., Ltd., Choshi, Japan.

出版信息

J Pharmacobiodyn. 1991 Jun;14(6):293-300. doi: 10.1248/bpb1978.14.293.

Abstract

The in vivo and in vitro effects of platelet-activating factor (PAF, 1-O-hexadecyl-2-acetyl-sn-glycero-3-phosphorylcholine) and acetylcholine (ACh) on vascular relaxation responses were examined in streptozotocin-induced diabetic rats. Intravenous injection of PAF and ACh (0.03 to 10 micrograms/kg) decreased the mean blood pressure in both control and diabetic rats in a dose-dependent fashion. Initial blood pressure in diabetic rats did not significantly differ from that in control rats. However, depressor responses induced by PAF and ACh in diabetic rats were attenuated more than those in control rats. In perfused mesenteric arterial bed preconstricted with methoxamine (10(-5) - 10(-4) M), PAF (10(-11) -3 x 10(-10) M) produced a concentration-dependent relaxation. However, this relaxation was significantly attenuated in the diabetic preparation compared with the control preparation. ACh also produced a concentration-dependent vasodilation in perfused mesenteric arterial bed. The concentration-response curve for the relaxation of the mesenteric arterial bed to ACh in diabetic preparation was shifted to the right compared with that in control preparation. A pretreatment with oxyhaemoglobin (10(-6) M) also shifted the concentration-response curves for relaxation to ACh in both control and diabetic preparation to the right. There was no difference in relaxation induced by sodium nitroprusside between the diabetic and the control preparation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在链脲佐菌素诱导的糖尿病大鼠中,研究了血小板活化因子(PAF,1-十六烷基-2-乙酰基-sn-甘油-3-磷酸胆碱)和乙酰胆碱(ACh)对血管舒张反应的体内和体外作用。静脉注射PAF和ACh(0.03至10微克/千克)可使对照大鼠和糖尿病大鼠的平均血压呈剂量依赖性下降。糖尿病大鼠的初始血压与对照大鼠相比无显著差异。然而,PAF和ACh在糖尿病大鼠中诱导的降压反应比对照大鼠更减弱。在预先用甲氧明(10⁻⁵ - 10⁻⁴ M)预收缩的灌注肠系膜动脉床中,PAF(10⁻¹¹ - 3×10⁻¹⁰ M)产生浓度依赖性舒张。然而,与对照制剂相比,糖尿病制剂中的这种舒张明显减弱。ACh在灌注肠系膜动脉床中也产生浓度依赖性血管舒张。糖尿病制剂中肠系膜动脉床对ACh舒张的浓度-反应曲线与对照制剂相比向右移动。用氧合血红蛋白(10⁻⁶ M)预处理也使对照和糖尿病制剂中对ACh舒张的浓度-反应曲线向右移动。糖尿病制剂和对照制剂之间硝普钠诱导的舒张没有差异。(摘要截断于250字)

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