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前列腺素E2在犬胃窦胆碱能介导的糖蛋白合成中的作用。

Role of prostaglandin E2 in cholinergic-mediated glycoprotein synthesis in canine antrum.

作者信息

Yoshimura K, Kraus E R, Shimakura S, Scheiman J M, Boland C R

机构信息

Department of Internal Medicine, VA Medical Center, Ann Arbor, Michigan.

出版信息

Dig Dis Sci. 1992 Jul;37(7):1045-50. doi: 10.1007/BF01300285.

Abstract

We studied the mechanism of cholinergic stimulation of mucin synthesis in canine antral explants, including the role of PGE2 as an intermediate messenger. Isolated antral mucosa was incubated with 10(-5) M carbachol (Cb), 10(-5) M indomethacin (IND), 10(-5) M pirenzepine (PZ), 10(-5) M Cb + 10(-5) M PZ, 10(-5) M Cb + 10(-5) M IND, and 10(-5) M IND + PGE2 (10(-8), 10(-7) and 10(-6) M) in the presence or absence of [3H]glucosamine. After 24 hr, total glycoprotein synthesis was quantitated by Sepharose-4B chromatography and by 10% TCA/1% PTA precipitation with lipid extraction. PGE2 released into the media was measured by radioimmunoassay (RIA). Cb significantly increased total glycoprotein synthesis and produced a significant increase in PGE2 release. The increase in glycoprotein synthesis and the release of PGE2 was blocked by the addition of muscarinic antagonist PZ. The addition of IND significantly inhibited glycoprotein synthesis and almost entirely suppressed PGE2 secretion. IND also inhibited the effect of Cb on glycoprotein synthesis and PGE2 release. Moreover, PGE2 (10(-6) and 10(-7) M) significantly increased the glycoprotein synthesis in the canine stomach. This suggests the coordinate participation of PGE2-releasing cell population in modulation of glycoprotein synthesis in gastric mucosa.

摘要

我们研究了胆碱能刺激犬胃窦外植体中粘蛋白合成的机制,包括前列腺素E2(PGE2)作为中间信使的作用。将分离的胃窦黏膜与10(-5)M卡巴胆碱(Cb)、10(-5)M吲哚美辛(IND)、10(-5)M哌仑西平(PZ)、10(-5)M Cb + 10(-5)M PZ、10(-5)M Cb + 10(-5)M IND以及10(-5)M IND + PGE2(10(-8)、10(-7)和10(-6)M)一起孵育,孵育时存在或不存在[3H]葡糖胺。24小时后,通过琼脂糖-4B色谱法以及用脂质提取的10%三氯乙酸/1%磷钨酸沉淀法对总糖蛋白合成进行定量。通过放射免疫测定法(RIA)测量释放到培养基中的PGE2。Cb显著增加了总糖蛋白合成,并使PGE2释放显著增加。添加毒蕈碱拮抗剂PZ可阻断糖蛋白合成的增加和PGE2的释放。添加IND显著抑制了糖蛋白合成,并几乎完全抑制了PGE2的分泌。IND还抑制了Cb对糖蛋白合成和PGE2释放的作用。此外,PGE2(10(-6)和10(-7)M)显著增加了犬胃中的糖蛋白合成。这表明释放PGE2的细胞群体协同参与胃黏膜中糖蛋白合成的调节。

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