Yamada S, Takauchi K, Itami T, Miyamoto T, Tsukatani H
J Pharmacobiodyn. 1980 Aug;3(8):367-73. doi: 10.1248/bpb1978.3.367.
Cardiovascular action of "peritoneal dialysate-depressor-I" (PD.D-I), a short-acting hypotensive phospholipid occurring in dog peritoneal dialysate, was investigated. With an intravenous injection of PD.D-I into an anaesthetized rat, a sharp fall of arterial blood pressure was observed and the effects were dose dependent. The maximum hypotensive effect was about 60 mmHg and the minimum effective dose was approximately 35 micrograms/kg. Neither tachyphylaxis nor sensitization was observed. Even in conscious rats PD.D-I elicited hypotensive responses, though the effect was much weaker than that produced in anaesthetized rats. In spinal rats the hypotensive effects were also observed. In the tests on rats reserpinized or pretreated with antimuscarinic, antihistaminic, beta-adrenergic-blocking and ganglionic-blocking agents, the depressor effect of PD.D-I was not affected. PD.D-I elicited also hypotensive responses in anaesthetized cats, rabbits and guinea pigs in the same degree as those in anaesthetized rats. The relaxation of the peripheral blood vessels was observed in the test on perfused rabbit ear. The depressor factor showed no smooth muscle stimulating activity in isolated guinea pig ileum preparations. Judging from these findings, the hypotensive effect of PD.D-I is not ascribable to the central, sympathetic or parasympathetic nervous system but possibly to direct action on the peripheral vascular system.
对存在于犬腹膜透析液中的一种短效降压磷脂“腹膜透析液降压因子-I”(PD.D-I)的心血管作用进行了研究。给麻醉大鼠静脉注射PD.D-I后,观察到动脉血压急剧下降,且作用呈剂量依赖性。最大降压作用约为60 mmHg,最小有效剂量约为35微克/千克。未观察到快速耐受性或致敏现象。即使在清醒大鼠中,PD.D-I也能引起降压反应,尽管其作用比在麻醉大鼠中产生的作用弱得多。在脊髓大鼠中也观察到了降压作用。在用利血平处理或用抗毒蕈碱、抗组胺、β-肾上腺素能阻断和神经节阻断剂预处理的大鼠试验中,PD.D-I的降压作用不受影响。PD.D-I在麻醉猫、兔和豚鼠中也引起了与麻醉大鼠相同程度的降压反应。在灌注兔耳试验中观察到外周血管舒张。在离体豚鼠回肠制备物中,该降压因子未显示平滑肌刺激活性。从这些发现判断,PD.D-I的降压作用不归因于中枢、交感或副交感神经系统,而可能是对外周血管系统的直接作用。