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自发性高血压大鼠的血压变化与主动脉前列环素的生成相关。

Blood pressure changes in spontaneously hypertensive rats correlate with aortic prostacyclin formation.

作者信息

Fahr A, Förster W, Taube C

出版信息

Br J Pharmacol. 1983 May;79(1):19-21. doi: 10.1111/j.1476-5381.1983.tb10490.x.

DOI:10.1111/j.1476-5381.1983.tb10490.x
PMID:6347301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2044827/
Abstract

1 The relationship between the blood pressure fall, induced by antihypertensive drugs or bleeding, and the formation of prostacyclin (PGI2)-like activity in the thoracic aorta of spontaneously hypertensive rats has been investigated. Inhibition of ADP-induced platelet aggregation was used to assess PGI2-like activity. 2 The decreases in blood pressure produced by clonidine, dihydralazine and prazosin were associated with increases of PGI2-like activity of 50-80%. The increase in PGI2-like activity correlated well with the blood pressure decrease, independently of the mechanism of the fall in blood pressure.

摘要
  1. 已经研究了抗高血压药物或放血诱导的血压下降与自发性高血压大鼠胸主动脉中前列环素(PGI2)样活性形成之间的关系。使用抑制ADP诱导的血小板聚集来评估PGI2样活性。2. 可乐定、双肼屈嗪和哌唑嗪引起的血压下降与PGI2样活性增加50 - 80%相关。PGI2样活性的增加与血压下降密切相关,与血压下降的机制无关。

相似文献

1
Blood pressure changes in spontaneously hypertensive rats correlate with aortic prostacyclin formation.自发性高血压大鼠的血压变化与主动脉前列环素的生成相关。
Br J Pharmacol. 1983 May;79(1):19-21. doi: 10.1111/j.1476-5381.1983.tb10490.x.
2
The role of TXA2 in hypertension.
Biomed Biochim Acta. 1984;43(8-9):S208-11.
3
Ontogeny of aortic PGI2 formation in the developing spontaneously hypertensive rat--correlation with elevations in blood pressure.自发性高血压大鼠发育过程中主动脉前列环素生成的个体发生——与血压升高的相关性
Adv Prostaglandin Thromboxane Res. 1980;7:797-801.
4
Influence of acetylsalicylic acid and BM 13177 on blood pressure and efficacy of antihypertensive drugs in spontaneously hypertensive rats.乙酰水杨酸和BM 13177对自发性高血压大鼠血压及抗高血压药物疗效的影响。
Biomed Biochim Acta. 1988;47(10-11):S94-9.
5
Antihypertensive effect of prostacyclin (PGI2) in experimental hypertension and its influence on plasma renin activity in rats.前列环素(PGI2)在实验性高血压中的降压作用及其对大鼠血浆肾素活性的影响。
Prostaglandins Med. 1978 Nov;1(5):359-72. doi: 10.1016/0161-4630(78)90123-4.
6
Prostaglandin I2 has more potent hypotensive properties than prostaglandin E2 in the normal and spontaneously hypertensive rat.在正常大鼠和自发性高血压大鼠中,前列腺素I2比前列腺素E2具有更强的降压特性。
Prostaglandins. 1978 Jun;15(6):999-1003. doi: 10.1016/0090-6980(78)90042-4.
7
Effect of trapidil on prostacyclin generation of arterial wall.曲匹地尔对动脉壁前列环素生成的影响。
Prostaglandins Med. 1980 Aug;5(2):113-21. doi: 10.1016/0161-4630(80)90098-1.
8
Changes of prostaglandin synthesis in aorta, brain and kidney medulla of normal rats treated with antihypertensive drugs.
Acta Biol Med Ger. 1978;37(5-6):889-90.
9
Vascular smooth muscle reactivity to rabbit aorta contracting substance (RCS) and production of prostacyclin-like substance in normotensive and hypertensive rats.正常血压和高血压大鼠血管平滑肌对兔主动脉收缩物质(RCS)的反应及前列环素样物质的产生。
Jpn Circ J. 1981 Jun;45(6):680-6. doi: 10.1253/jcj.45.680.
10
Enhanced formation of PGI2, a potent hypotensive substance, by aortic rings and homogenates of the spontaneously hypertensive rat.自发性高血压大鼠的主动脉环和匀浆中强效降压物质前列环素(PGI2)的生成增强。
Prostaglandins. 1978 Jun;15(6):1005-12. doi: 10.1016/0090-6980(78)90043-6.

本文引用的文献

1
PGI2-specific antibodies administered in vivo suggest against a role for endogenous PGI2 as a circulating vasodepressor hormone in the normotensive and spontaneously hypertensive rat.体内注射前列环素(PGI2)特异性抗体表明,内源性PGI2在正常血压和自发性高血压大鼠中并非作为循环血管舒张激素发挥作用。
Prostaglandins. 1980 Dec;20(6):1053-60. doi: 10.1016/0090-6980(80)90059-3.
2
Prostacyclin reversal of aspirin and indomethacin effects on blood pressure responses to norepinephrine.前列环素对阿司匹林和吲哚美辛影响去甲肾上腺素所致血压反应的逆转作用。
Pharmacol Res Commun. 1980 Apr;12(4):319-28. doi: 10.1016/s0031-6989(80)80088-9.
3
Effects of prostaglandins E2, I2 and F2 alpha, arachidonic acid and indomethacin on pressor responses to norepinephrine in conscious rats.前列腺素E2、I2和F2α、花生四烯酸及吲哚美辛对清醒大鼠去甲肾上腺素升压反应的影响
Prostaglandins. 1980 Jun;19(6):855-64. doi: 10.1016/0090-6980(80)90119-7.
4
PGI2 inhibits ischemia-induced platelet activation and prevents myocardial damage by inhibition of catecholamine release from adrenergic nerve terminals. Evidence for cAMP as common denominator.前列环素(PGI2)可抑制缺血诱导的血小板活化,并通过抑制肾上腺素能神经末梢释放儿茶酚胺来预防心肌损伤。以环磷酸腺苷(cAMP)作为共同特征的证据。
Thromb Res. 1981;21(1-2):175-80. doi: 10.1016/0049-3848(84)90046-x.
5
Prostaglandin I2 has more potent hypotensive properties than prostaglandin E2 in the normal and spontaneously hypertensive rat.在正常大鼠和自发性高血压大鼠中,前列腺素I2比前列腺素E2具有更强的降压特性。
Prostaglandins. 1978 Jun;15(6):999-1003. doi: 10.1016/0090-6980(78)90042-4.
6
Enhanced formation of PGI2, a potent hypotensive substance, by aortic rings and homogenates of the spontaneously hypertensive rat.自发性高血压大鼠的主动脉环和匀浆中强效降压物质前列环素(PGI2)的生成增强。
Prostaglandins. 1978 Jun;15(6):1005-12. doi: 10.1016/0090-6980(78)90043-6.
7
Sympathetic nerve activity: role in regulation of blood pressure in the spontaenously hypertensive rat.交感神经活动:在自发性高血压大鼠血压调节中的作用
Circ Res. 1976 Jun;38(6 Suppl 2):21-9. doi: 10.1161/01.res.38.6.21.