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C-6胶质瘤在体内对异丙肾上腺素和罂粟碱的反应取决于β-肾上腺素能受体密度。

Response of C-6 glioma to isoproterenol and papaverine in vivo depends on beta-adrenergic receptor density.

作者信息

Chelmicka-Schorr E, Sportiello M G, Atweh S F, Arnason B G

出版信息

Ann Neurol. 1984 Jan;15(1):96-9. doi: 10.1002/ana.410150117.

DOI:10.1002/ana.410150117
PMID:6324652
Abstract

Rat C-6 glioma serves as an experimental model for human glioma. C-6 glioma cells carried to high culture passages in medium containing 10% fetal bovine serum when injected in vivo are unresponsive to treatment with the beta-adrenergic agonist isoproterenol and the phosphodiesterase inhibitor papaverine. When C-6 glioma cells are kept in culture in serum-containing medium, beta-adrenergic receptor density falls and, concomitantly, ability to accumulate cyclic adenosine monophosphate in response to stimulation with catecholamines declines. Responsiveness to treatment in vivo with a beta-adrenergic agonist was restored when C-6 glioma cells were cultured in serum-free defined medium prior to systemic injection into rats. Culturing of C-6 glioma cells in serum-free medium significantly increases the number of beta-adrenergic receptors when compared with C-6 glioma cells grown in serum-containing medium.

摘要

大鼠C-6胶质瘤可作为人类胶质瘤的实验模型。当在含有10%胎牛血清的培养基中传代培养至高代数后,将C-6胶质瘤细胞注射到体内时,它们对β-肾上腺素能激动剂异丙肾上腺素和磷酸二酯酶抑制剂罂粟碱的治疗无反应。当C-6胶质瘤细胞在含血清的培养基中培养时,β-肾上腺素能受体密度下降,同时,对儿茶酚胺刺激产生反应而积累环磷酸腺苷的能力也下降。当C-6胶质瘤细胞在全身注射到大鼠体内之前,先在无血清限定培养基中培养时,其对β-肾上腺素能激动剂体内治疗的反应性得以恢复。与在含血清培养基中生长的C-6胶质瘤细胞相比,在无血清培养基中培养C-6胶质瘤细胞可显著增加β-肾上腺素能受体的数量。

相似文献

1
Response of C-6 glioma to isoproterenol and papaverine in vivo depends on beta-adrenergic receptor density.C-6胶质瘤在体内对异丙肾上腺素和罂粟碱的反应取决于β-肾上腺素能受体密度。
Ann Neurol. 1984 Jan;15(1):96-9. doi: 10.1002/ana.410150117.
2
[Treatment of rat glioma with a beta-adrenergic agonist and a phosphodiesterase inhibitor in vivo].[体内使用β-肾上腺素能激动剂和磷酸二酯酶抑制剂治疗大鼠神经胶质瘤]
No To Shinkei. 1987 Aug;39(8):719-23.
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C-6 glioma growth in rats: suppression with a beta-adrenergic agonist and a phosphodiesterase inhibitor.大鼠C-6胶质瘤生长:用β-肾上腺素能激动剂和磷酸二酯酶抑制剂抑制
Ann Neurol. 1980 Oct;8(4):447-9. doi: 10.1002/ana.410080421.
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Growth of C6 glioma cells in serum-containing medium decreases beta-adrenergic receptor number.C6胶质瘤细胞在含血清培养基中的生长会减少β-肾上腺素能受体的数量。
J Cell Physiol. 1981 Nov;109(2):309-15. doi: 10.1002/jcp.1041090214.
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Modulation of beta-adrenergic response in rat brain astrocytes by serum and hormones.血清和激素对大鼠脑星形胶质细胞β-肾上腺素能反应的调节
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Ca2+ inhibition of beta-adrenergic receptor- and forskolin-stimulated cAMP accumulation in C6-2B rat glioma cells is independent of protein kinase C.钙离子对C6-2B大鼠胶质瘤细胞中β-肾上腺素能受体和福斯高林刺激的环磷酸腺苷积累的抑制作用与蛋白激酶C无关。
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Neuroblastoma membranes inhibit isoproterenol-stimulated rise of cAMP in glioma cells.神经母细胞瘤细胞膜可抑制异丙肾上腺素刺激的胶质瘤细胞中cAMP水平升高。
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Does diethylstilbestrol (DES) change the stress fiber organization in C6 rat glioma cells?己烯雌酚(DES)会改变C6大鼠胶质瘤细胞中的应力纤维组织吗?
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Close reciprocal regulation of beta 1- and beta 2-adrenergic receptors by dexamethasone in C6 glioma cells: effects on catecholamine responsiveness.地塞米松对C6胶质瘤细胞中β1 -和β2 -肾上腺素能受体的相互紧密调节:对儿茶酚胺反应性的影响
Mol Pharmacol. 1993 Dec;44(6):1085-93.

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Reduced beta adrenoceptor density in vivo in human lung tumours: a preliminary study with positron emission tomography.人肺肿瘤体内β肾上腺素能受体密度降低:正电子发射断层扫描的初步研究
Thorax. 1996 Jul;51(7):727-32. doi: 10.1136/thx.51.7.727.