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体外培养的大鼠垂体前叶中强啡肽样免疫反应性的释放

Release of dynorphin-like immunoreactivity from rat anterior pituitary gland in vitro.

作者信息

Knepel W, Schwaninger M

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 Mar;329(1):94-6. doi: 10.1007/BF00695198.

DOI:10.1007/BF00695198
PMID:2860571
Abstract

Rat anterior pituitary quarters were incubated in vitro and the release of dynorphin A1-13-like immunoreactivity (Dyn A1-13-IR) into the incubation medium was studied. An elevation of the potassium concentration of the incubation medium to 40 mmol/l increased the release of Dyn A1-13-IR in a calcium-dependent manner. Addition of luteinizing hormone-releasing hormone (LHRH) stimulated the release of Dyn A1-13-IR in a dose-dependent manner. The LHRH-induced release of Dyn A1-13-IR was almost completely prevented by omission of calcium ions from the incubation medium or by addition of the LHRH-antagonist D-pGlu1,D-Phe2,D-Trp3,6-LHRH. This is the first demonstration that dynorphin-like immunoreactivity can be released from the rat adenohypophysis through calcium-dependent mechanisms by both high potassium concentration and receptor-mediated stimulation.

摘要

将大鼠垂体前叶切成小块进行体外培养,研究强啡肽A1 - 13样免疫反应性物质(Dyn A1 - 13 - IR)释放到培养液中的情况。将培养液中钾离子浓度提高到40 mmol/L,以钙依赖的方式增加了Dyn A1 - 13 - IR的释放。添加促黄体生成素释放激素(LHRH)以剂量依赖的方式刺激了Dyn A1 - 13 - IR的释放。培养液中钙离子缺失或添加LHRH拮抗剂D - pGlu1,D - Phe2,D - Trp3,6 - LHRH几乎完全抑制了LHRH诱导的Dyn A1 - 13 - IR释放。这首次证明了强啡肽样免疫反应性物质可通过高钾浓度和受体介导的刺激,经钙依赖机制从大鼠腺垂体释放。

相似文献

1
Release of dynorphin-like immunoreactivity from rat anterior pituitary gland in vitro.体外培养的大鼠垂体前叶中强啡肽样免疫反应性的释放
Naunyn Schmiedebergs Arch Pharmacol. 1985 Mar;329(1):94-6. doi: 10.1007/BF00695198.
2
Corelease of dynorphin-like immunoreactivity, luteinizing hormone, and follicle-stimulating hormone from rat adenohypophysis in vitro.体外大鼠腺垂体中强啡肽样免疫反应性物质、促黄体生成素和促卵泡激素的共同释放
Endocrinology. 1985 Aug;117(2):481-7. doi: 10.1210/endo-117-2-481.
3
Effect of human growth hormone-releasing hormone on the release of dynorphin-like immunoreactivity, luteinizing hormone, and follicle-stimulating hormone from rat adenohypophysis in vitro.人生长激素释放激素对体外培养的大鼠腺垂体中强啡肽样免疫反应物质、促黄体生成素和促卵泡激素释放的影响。
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4
Release of dynorphin-like immunoreactivity from rat adenohypophysis in vitro during inhibition of anterior pituitary hormone secretion from individual cell types.在体外抑制大鼠腺垂体单个细胞类型的前叶垂体激素分泌过程中,大鼠腺垂体中强啡肽样免疫反应性的释放。
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Angiotensin II is retained in gonadotrophs of pituitary cell aggregates cultured in serum-free medium but does not mimic the effects of exogenous angiotensins and luteinizing-hormone-releasing hormone on growth hormone release.血管紧张素II保留在无血清培养基中培养的垂体细胞聚集体的促性腺激素细胞中,但不能模拟外源性血管紧张素和促黄体生成激素释放激素对生长激素释放的影响。
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Neuropeptide-Y enhances luteinizing hormone (LH)-releasing hormone-induced LH release and elevations in cytosolic Ca2+ in rat anterior pituitary cells: evidence for involvement of extracellular Ca2+ influx through voltage-sensitive channels.神经肽Y增强促黄体生成素(LH)释放激素诱导的大鼠垂体前叶细胞LH释放及胞质Ca2+升高:通过电压敏感性通道的细胞外Ca2+内流参与的证据。
Endocrinology. 1990 Sep;127(3):1487-94. doi: 10.1210/endo-127-3-1487.
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Immunoreactive dynorphin-A in ovine anterior pituitary and effects of estradiol-17 beta administration.绵羊垂体前叶中的免疫反应性强啡肽 -A 及 17β-雌二醇给药的影响
Peptides. 1987 Mar-Apr;8(2):367-9. doi: 10.1016/0196-9781(87)90113-6.

本文引用的文献

1
Gonadotropin-releasing hormone: molecular and cell biology, physiology, and clinical applications.促性腺激素释放激素:分子与细胞生物学、生理学及临床应用
Fed Proc. 1984 Jun;43(9):2351-61.
2
In vitro adrenocorticotropin/beta-endorphin-releasing activity of vasopressin analogs is related neither to pressor nor to antidiuretic activity.血管加压素类似物的体外促肾上腺皮质激素/β-内啡肽释放活性既与升压活性无关,也与抗利尿活性无关。
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3
Relative contents and concomitant release of prodynorphin/neoendorphin-derived peptides in rat hippocampus.
大鼠海马中前强啡肽/新内啡肽衍生肽的相对含量及伴随释放
Proc Natl Acad Sci U S A. 1983 Dec;80(24):7669-73. doi: 10.1073/pnas.80.24.7669.
4
Regional distribution of dynorphin and neo-endorphin peptides in rat brain, spinal cord, and pituitary.强啡肽和新内啡肽肽在大鼠脑、脊髓和垂体中的区域分布。
J Neurosci. 1983 Nov;3(11):2146-52. doi: 10.1523/JNEUROSCI.03-11-02146.1983.
5
Concomitant neonatal development and in vitro release of dynorphin and alpha-neo-endorphin.强啡肽和α-新内啡肽的伴随性新生儿发育及体外释放
Life Sci. 1982;31(16-17):1757-60. doi: 10.1016/0024-3205(82)90203-x.
6
Release of dynorphin-like immunoreactivity of rat neurohypophysis in comparison to vasopressin after various stimuli in vitro and in vivo.与抗利尿激素相比,大鼠神经垂体中强啡肽样免疫反应性在体内外各种刺激后的释放情况。
Neurosci Lett. 1982 Aug 16;31(2):159-64. doi: 10.1016/0304-3940(82)90109-4.
7
Dynorphin and dynorphin are ligands for the kappa-subtype of opiate receptor.
Nature. 1982 Sep 2;299(5878):79-81. doi: 10.1038/299079a0.
8
Dynorphin is a specific endogenous ligand of the kappa opioid receptor.强啡肽是κ阿片受体的特异性内源性配体。
Science. 1982 Jan 22;215(4531):413-5. doi: 10.1126/science.6120570.
9
Immunoreactive dynorphin in the rat adenohypophysis consists exclusively of 6000 dalton species.大鼠腺垂体中的免疫反应性强啡肽仅由6000道尔顿的成分组成。
Biochem Biophys Res Commun. 1981 Nov 16;103(1):256-63. doi: 10.1016/0006-291x(81)91687-9.
10
Dynorphin immunocytochemical localization in brain and peripheral nervous system: preliminary studies.强啡肽在脑和外周神经系统中的免疫细胞化学定位:初步研究。
Proc Natl Acad Sci U S A. 1981 Feb;78(2):1260-3. doi: 10.1073/pnas.78.2.1260.