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组胺及环磷酸腺苷系统激活剂对分离的胃非壁细胞中蛋白质合成及高分子量糖蛋白释放的影响。

Effects of histamine and activators of the cyclic AMP system on protein synthesis in and release of high molecular weight glycoproteins from isolated gastric non-parietal cells.

作者信息

Heim H K, Oestmann A, Sewing K F

机构信息

Institut für Allgemeine Pharmakologie, Medizinische Hochschule Hannover, Germany.

出版信息

Br J Pharmacol. 1991 Oct;104(2):526-30. doi: 10.1111/j.1476-5381.1991.tb12462.x.

Abstract
  1. Glycoprotein and protein synthesis in and release from pig isolated, enriched gastric mucous cells were measured by the incorporation of N-acetyl-[14C]-D-glucosamine and [3H]-L-leucine, respectively, into cellular and released acid precipitable material. 2. Histamine and activators of the adenosine 3':5'-cyclic monophosphate (cyclic AMP) system maximally stimulated total protein and glycoprotein synthesis in and release from the cells at concentrations of histamine (10 microM), forskolin (10-100 microM), 3-isobutyl-1-methylxanthine (100 microM), and dibutyryl cyclic AMP (1-3 mM), respectively. In the presence of 3-isobutyl-1-methylxanthine (30 microM) histamine stimulation was enhanced. 3. As shown by gel chromatography, stimulation by histamine (100 microM), forskolin (10 microM), 3-isobutyl-1-methylxanthine (100 microM) and dibutyryl cyclic AMP (1 mM) resulted in a release of high molecular weight (approximately 2 x 10(6) daltons) glycoproteins from the cells. The histamine H2-receptor antagonist, ranitidine (100 microM), blocked the effect of histamine. 4. We conclude that cyclic AMP-dependent processes are involved in the regulation of protein and glycoprotein synthesis in and the release of high molecular weight (mucous) glycoproteins from pig gastric non-parietal cells and that histamine may be a physiological activator of this system.
摘要
  1. 通过分别将N-乙酰-[14C]-D-葡萄糖胺和[3H]-L-亮氨酸掺入细胞内及释放的酸沉淀物质中,测定猪分离的富集胃黏液细胞中的糖蛋白和蛋白质合成以及从这些细胞中的释放情况。2. 组胺和腺苷3':5'-环磷酸腺苷(环磷酸腺苷)系统的激活剂分别在组胺浓度为10微摩尔、福斯可林浓度为10 - 100微摩尔、3-异丁基-1-甲基黄嘌呤浓度为100微摩尔以及二丁酰环磷酸腺苷浓度为1 - 3毫摩尔时,最大程度地刺激了细胞内的总蛋白质和糖蛋白合成以及从细胞中的释放。在存在3-异丁基-1-甲基黄嘌呤(30微摩尔)的情况下,组胺刺激增强。3. 如凝胶色谱所示,组胺(100微摩尔)、福斯可林(10微摩尔)、3-异丁基-1-甲基黄嘌呤(100微摩尔)和二丁酰环磷酸腺苷(1毫摩尔)的刺激导致细胞释放出高分子量(约2×10(6)道尔顿)的糖蛋白。组胺H2受体拮抗剂雷尼替丁(100微摩尔)阻断了组胺的作用。4. 我们得出结论,环磷酸腺苷依赖性过程参与了猪胃非壁细胞中蛋白质和糖蛋白合成的调节以及高分子量(黏液)糖蛋白的释放,并且组胺可能是该系统的生理激活剂。

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Pepsinogen release from isolated gastric glands.从分离的胃腺中释放胃蛋白酶原。
Am J Physiol. 1982 Sep;243(3):G218-25. doi: 10.1152/ajpgi.1982.243.3.G218.

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