α-lactorphin lowers blood pressure measured by radiotelemetry in normotensive and spontaneously hypertensive rats

被引:132
作者
Nurminen, ML
Sipola, M
Kaarto, H
Pihlanto-Leppälä, A
Piilola, K
Korpela, R
Tossavainen, O
Korhonen, H
Vapaatalo, H
机构
[1] Univ Helsinki, Inst Biomed, Dept Pharmacol & Toxicol, FIN-00014 Helsinki, Finland
[2] Agr Res Ctr Finland, FIN-31600 Jokioinen, Finland
[3] Valio Ltd, Res & Dev, FIN-00039 Helsinki, Finland
关键词
alpha-lactorphin; blood pressure; radiotelemetry; SHR; opioid receptors; naloxone; HOE; 140;
D O I
10.1016/S0024-3205(00)00471-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cardiovascular effects of subcutaneous administration of synthetic alpha-lactorphin, a tetrapeptide (Tyr-Gly-Leu-Phe) originally derived from milk alpha-lactalbumin, were studied in conscious spontaneously hypertensive rats (SHR) and in normotensive Wistar Kyoto rats (WKY) with continuous radiotelemetric monitoring. alpha-Lactorphin dose-dependently lowered blood pressure (BP) without affecting heart rate in SHR and WKY. The lowest dose which reduced BP was 10 mu g/kg, and the maximal reductions in systolic and diastolic BP (by 23+/-4 and 17+/-4 mm Hg, respectively) were observed at 100 mu g/kg dose in SHR. No further reductions were obtained at a higher dose of 1 mg/kg. There were no significant differences in the BP responses to alpha-lactorphin between SHR and WKY. Naloxone (1 and 3 mg/kg s.c.), a specific opioid receptor antagonist, abolished the alpha-lactorphin-induced reduction in BP and reversed it into a presser response, which provides evidence for an involvement of opioid receptors in the depressor action of the tetrapeptide.
引用
收藏
页码:1535 / 1543
页数:9
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