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P物质对去甲肾上腺素诱导的大鼠肠系膜血管收缩反应的调节作用。

Modulatory effects of substance P on norepinephrine induced vasoconstrictor responses in the rat mesentery.

作者信息

Gulati N, Huggel H, Gulati O P

出版信息

Gen Pharmacol. 1983;14(1):157-60. doi: 10.1016/0306-3623(83)90090-3.

Abstract
  1. The role of substance P (SP) in adrenergic transmission has been studied in the isolated perfused rat mesentery. 2. Intra-arterial perfusion of SP (4 x 10(-9) to 4 x 10(-7)M) produced a dose dependent potentiation of norepinephrine (NE) induced vasoconstrictor responses and a shift of the log dose--response curve to the left. 3. Saralasin, a specific antagonist of angiotensin II (ang. II) when perfused at a concentration of 3 x 10(-9)M did not change the NE responses as such. However, the potentiating effect of SP could not be demonstrated in the presence of saralasin. 4. Indomethacin, a prostaglandin (PG) synthetase inhibitor, when perfused at a concentration of 2.8 x 10(-6)M, markedly attenuated the vascular responses to NE, which could not be normalized by the addition of SP. 5. It appears that SP's potentiating effect on NE responses in the perfused rat mesentery simulates ang. II and not prostaglandins. A direct non-specific post synaptic sensitizing effect of SP on vascular smooth muscle cell, for its potentiating property, cannot be ruled out.
摘要
  1. 已在离体灌注大鼠肠系膜中研究了P物质(SP)在肾上腺素能传递中的作用。2. 动脉内灌注SP(4×10⁻⁹至4×10⁻⁷M)产生去甲肾上腺素(NE)诱导的血管收缩反应的剂量依赖性增强,并使对数剂量-反应曲线向左移动。3. 血管紧张素II(ang. II)的特异性拮抗剂沙拉新,当以3×10⁻⁹M的浓度灌注时,本身并不改变NE反应。然而,在沙拉新存在的情况下,SP的增强作用无法得到证实。4. 前列腺素(PG)合成酶抑制剂吲哚美辛,当以2.8×10⁻⁶M的浓度灌注时,显著减弱了对NE的血管反应,添加SP也无法使其恢复正常。5. 似乎SP对灌注大鼠肠系膜中NE反应的增强作用模拟了ang. II而非前列腺素。不能排除SP因其增强特性对血管平滑肌细胞产生直接的非特异性突触后致敏作用。

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