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血小板活化因子对离体豚鼠回肠的双相作用。

Biphasic action of platelet-activating factor on isolated guinea-pig ileum.

作者信息

Tokumura A, Harada K, Fukuzawa K, Tsukatani H

出版信息

Lipids. 1983 Nov;18(11):848-50. doi: 10.1007/BF02534647.

Abstract

1-0-Hexadecyl-2-0-acetyl-sn-glycero-3-phosphocholine (platelet-activating factor) at 10(-10)-10(-9) M induced slow contraction of isolated guinea-pig ileal muscles and the contraction persisted for a long time. At a higher concentration of 10(-7) M, this phospholipid induced more rapid, but not greater, contraction. At higher concentrations (10(-6)-10(-5) M), this phospholipid induced a biphasic response: rapid contraction followed by relaxation. At high concentrations, this compound inhibited acetyl-choline-induced contractions. The stimulatory effect of this phospholipid was ca. 300 times that of 1-palmitoyl-2-0-acetyl-sn-glycero-3-phosphocholine, while its inhibitory potency on induced contraction was similar to those of 1-palmitoyl-2-0-acetyl-sn-glycero-3-phosphocholine and its lyso derivative. It was suggested that the differences in effects on contraction of different concentrations of 1-0-hexadecyl- and 1-palmitoyl-2-0-acetyl-sn-glycero-3-phosphocholine were due to the effects of these compounds on the ileum: a strong stimulatory effect and a moderate inhibitory effect on contraction.

摘要

1-0-十六烷基-2-0-乙酰基-sn-甘油-3-磷酸胆碱(血小板活化因子)在10⁻¹⁰ - 10⁻⁹ M浓度时可诱导豚鼠离体回肠肌肉缓慢收缩,且该收缩持续较长时间。在10⁻⁷ M的较高浓度下,这种磷脂诱导的收缩更快,但幅度并未增大。在更高浓度(10⁻⁶ - 10⁻⁵ M)时,这种磷脂诱导双相反应:快速收缩后接着松弛。在高浓度时,该化合物抑制乙酰胆碱诱导的收缩。这种磷脂的刺激作用约为1-棕榈酰-2-0-乙酰基-sn-甘油-3-磷酸胆碱的300倍,而其对诱导收缩的抑制效力与1-棕榈酰-2-0-乙酰基-sn-甘油-3-磷酸胆碱及其溶血衍生物相似。有人认为,不同浓度的1-0-十六烷基-和1-棕榈酰-2-0-乙酰基-sn-甘油-3-磷酸胆碱对收缩作用的差异是由于这些化合物对回肠的作用:对收缩有强烈的刺激作用和适度的抑制作用。

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