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不同物种中血压和心脏组织对前列环素(PGI2)的反应。

Blood pressure and cardiac tissue responses to prostacyclin (PGI2) in various species.

作者信息

Collins G A, MacLeod B A, Walker M J

出版信息

Can J Physiol Pharmacol. 1982 Feb;60(2):134-9. doi: 10.1139/y82-022.

Abstract

The effect of prostacyclin (PGI2) on blood pressure and heart rate (in vivo) and on isolated heart tissue has been investigated in different species. Isolated cardiac tissue had limited responses to PGI2 tested at 10(-13) to 10(-5) M. Cultured neonatal rat heart cells did not respond to PGI2, neither did intact rat hearts or rabbit cardiac tissue. Guinea pig and rat atria showed limited dose-dependent responses to PGI2 at concentrations greater than 10(7) M. In rat atria, 10(-5) M PGI2 produced a limited elevation of tissue cAMP content. When given by intravenous injection or infusion, PGI2 produced hypotension in anaesthetized primates (three species), rat, rabbit, pig, and dog. As a vasodepressor in all species, PGI2 (on a weight basis) was more active than prostaglandins of the B or E type and, in most species tested, it was approximately five times more active than PGE2. Heart responses in intact animals were often paradoxical in that decreases in heart rate often accompanied blood pressure falls.

摘要

已在不同物种中研究了前列环素(PGI2)对血压和心率(体内)以及对离体心脏组织的影响。在10^(-13)至10^(-5)M浓度下测试时,离体心脏组织对PGI2的反应有限。培养的新生大鼠心脏细胞对PGI2无反应,完整的大鼠心脏或兔心脏组织也无反应。豚鼠和大鼠心房在浓度大于10^(-7)M时对PGI2表现出有限的剂量依赖性反应。在大鼠心房中,10^(-5)M PGI2使组织cAMP含量略有升高。经静脉注射或输注时,PGI2可使麻醉的灵长类动物(三种)、大鼠、兔、猪和狗出现低血压。作为所有物种的血管降压药,PGI2(按重量计)比B型或E型前列腺素更具活性,并且在大多数测试物种中,其活性约为PGE2的五倍。完整动物的心脏反应常常自相矛盾,即心率下降常常伴随血压下降。

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