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在人体前臂离体静脉中,抑制前列腺素合成并不影响对去甲肾上腺素、5-羟色胺、血管紧张素II和内皮素-1的收缩反应。

Inhibition of prostaglandin synthesis does not affect contractile responses to noradrenaline, serotonin, angiotensin II nor endothelin-1 in human forearm isolated veins.

作者信息

Chin J P, Hurlston R M, Dart A M

机构信息

Alfred and Baker Medical Unit, Baker Medical Research Institute, Commercial Road, Prahran, Victoria 3181, Australia.

出版信息

Br J Clin Pharmacol. 1993 Oct;36(4):303-7. doi: 10.1111/j.1365-2125.1993.tb00368.x.

Abstract
  1. The functional role of endogenous cyclo-oxygenase products was examined in the human forearm isolated vein. 2. Six healthy normal adult males (age > 18 years old) were recruited. Forearm veins were biopsied and ring segments mounted in standard organ baths for recording of isometric force. 3. Noradrenaline (-log molar EC50: 7.75 +/- 0.19; -log molar threshold concentration: 8.80 +/- 0.20), 5-hydroxytryptamine (-log molar EC50: 7.52 +/- 0.17; -log molar threshold concentration: 9.50 +/- 0.64), angiotensin II (-log molar threshold concentration: 9.00 +/- 0.28) and endothelin-1 (-log molar threshold concentration: 9.13 +/- 0.47) were equipotent in this preparation. Indomethacin (10 microM) had no effect on either the threshold concentration or EC50 of noradrenaline, 5-hydroxytryptamine nor the threshold concentration of angiotensin II nor endothelin-1. 4. Sodium nitroprusside (1 nM-10 microM) relaxed noradrenaline-precontracted preparations. Evidence of minimal endothelial influence was confirmed by the lack of relaxant response to acetylcholine (1 nM-10 microM). Histology using silver staining confirmed that endothelial cells were absent over greater than 90% of the lumen surface. 5. We conclude that endogenous prostanoids derived from smooth muscle cells, either released basally or agonist-stimulated, do not play a role in the regulation of vascular tone in the human forearm isolated vein.
摘要
  1. 在内源环氧化酶产物的功能作用在人前臂离体静脉中进行了研究。2. 招募了6名健康的正常成年男性(年龄>18岁)。取前臂静脉进行活检,并将环形节段安装在标准器官浴槽中以记录等长力。3. 去甲肾上腺素(-log摩尔EC50:7.75±0.19;-log摩尔阈浓度:8.80±0.20)、5-羟色胺(-log摩尔EC50:7.52±0.17;-log摩尔阈浓度:9.50±0.64)、血管紧张素II(-log摩尔阈浓度:9.00±0.28)和内皮素-1(-log摩尔阈浓度:9.13±0.47)在该制剂中效力相当。吲哚美辛(10μM)对去甲肾上腺素、5-羟色胺的阈浓度或EC50以及血管紧张素II和内皮素-1的阈浓度均无影响。4. 硝普钠(1 nM - 10μM)使去甲肾上腺素预收缩的制剂舒张。对乙酰胆碱(1 nM - 10μM)缺乏舒张反应证实了最小内皮影响的证据。银染色组织学证实超过90%的管腔表面没有内皮细胞。5. 我们得出结论,源自平滑肌细胞的内源性前列腺素,无论是基础释放还是激动剂刺激释放,在人前臂离体静脉的血管张力调节中不起作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19b3/1364682/2dc54c86dfe4/brjclinpharm00028-0036-a.jpg

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