Loredo J S, Gonzalez R R, Hessinger D A
J Pharmacol Exp Ther. 1985 Feb;232(2):301-4.
The purpose of this study was to characterize the mode of action of the venom from Portuguese man-of-war (Physalia physalis) on the skeletal muscle vascular bed of dogs anesthetized with sodium pentobarbital (35 mg/kg). Venous outflow and the blood pressure difference across the hind-limb vascular bed were used to calculate changes in resistance due to close arterial injections of the venom (0.001-1 microgram/kg). The venom consistently produced dilations that were blocked by sodium meclofenamate (5 mg/kg). Atropine (1 mg/kg), propranolol, phentolamine, cimetidine (each 2 mg/kg) or tripelennamine (2.5 mg/kg) had no significant blocking effect. The venom also produced transient dilations on vascular beds predilated with histamine or prostaglandin E1, or preconstricted with norepinephrine (each 0.01 microgram/kg) or by sympathetic stimulation (12 V, 20 Hz). These data suggest that Physalia venom dilates skeletal muscle vasculature primarily by stimulation of endogenous prostaglandin synthesis.
本研究的目的是表征葡萄牙僧帽水母(僧帽水母)毒液对用戊巴比妥钠(35毫克/千克)麻醉的犬骨骼肌血管床的作用方式。通过静脉流出量以及后肢血管床两端的血压差,来计算因近距离动脉注射毒液(0.001 - 1微克/千克)而导致的阻力变化。该毒液始终会引起血管舒张,且这种舒张会被甲氯芬那酸钠(5毫克/千克)阻断。阿托品(1毫克/千克)、普萘洛尔、酚妥拉明、西咪替丁(各2毫克/千克)或曲普利啶(2.5毫克/千克)均无显著阻断作用。该毒液还会对预先用组胺或前列腺素E1舒张,或预先用去甲肾上腺素(各0.01微克/千克)或交感神经刺激(12伏,20赫兹)收缩的血管床产生短暂的舒张作用。这些数据表明,僧帽水母毒液主要通过刺激内源性前列腺素合成来舒张骨骼肌血管系统。