吗啡可拮抗神经母细胞瘤细胞中前列腺素的作用，但对胶质瘤细胞以及胶质瘤与成纤维细胞杂交细胞中的前列腺素和去甲肾上腺素则无此作用。 - Suppr

Suppr

超能文献

Morphine antagonizes the action of prostaglandin in neuroblastoma cells but not of prostaglandin and noradrenaline in glioma and glioma times fibroblast hybrid cells.

作者信息

Traber J, Fischer K, Latzin S, Hamprecht B

出版信息

FEBS Lett. 1974 Dec 15;49(2):260-3. doi: 10.1016/0014-5793(74)80525-9.

DOI:10.1016/0014-5793(74)80525-9

PMID:4374398

Abstract

摘要

相似文献

Morphine antagonizes the action of prostaglandin in neuroblastoma cells but not of prostaglandin and noradrenaline in glioma and glioma times fibroblast hybrid cells.吗啡可拮抗神经母细胞瘤细胞中前列腺素的作用，但对胶质瘤细胞以及胶质瘤与成纤维细胞杂交细胞中的前列腺素和去甲肾上腺素则无此作用。

FEBS Lett. 1974 Dec 15;49(2):260-3. doi: 10.1016/0014-5793(74)80525-9.

Measurements of adenosine 3':5'-cyclic monophosphate and membrane potential in neuroblastoma times glioma hybrid cells: opiates and adrenergic agonists cause effects opposite to those of prostaglandin E1.神经母细胞瘤×胶质瘤杂交细胞中环磷酸腺苷及膜电位的测量：阿片类药物和肾上腺素能激动剂产生与前列腺素E1相反的效应。

FEBS Lett. 1975 Apr 1;52(2):327-32. doi: 10.1016/0014-5793(75)80836-2.

Morphine antagonises action of prostaglandin in neuroblastoma and neuroblastoma times glioma hybrid cells.吗啡可拮抗神经母细胞瘤及神经母细胞瘤与胶质瘤杂交细胞中前列腺素的作用。

Nature. 1975 Jan 10;253(5487):120-2. doi: 10.1038/253120a0.

Influence of noradrenalin, prostaglandin E1 and inhibitors of phosphodiesterase activity on levels of the cyclic adenosine 3':5'-monophosphate in somatic cell hybrids.去甲肾上腺素、前列腺素E1和磷酸二酯酶活性抑制剂对体细胞杂种中环磷酸腺苷3':5'-单磷酸水平的影响。

Hoppe Seylers Z Physiol Chem. 1973 Dec;354(12):1633-41. doi: 10.1515/bchm2.1973.354.2.1633.

Relationship between the actions of calcium ions, opiods, and prostaglandin E1 on the level of cyclic AMP in neuroblastoma x glioma hybrid cells.

J Neurochem. 1980 Mar;34(3):643-51. doi: 10.1111/j.1471-4159.1980.tb11192.x.

Cycloheximide potentiation of prostaglandin E1- and cholera toxin-stimulated cyclic AMP accumulation in NG108-CC15 neuroblastoma-glioma hybrid cells.放线菌酮对前列腺素E1和霍乱毒素刺激NG108-CC15神经母细胞瘤-胶质瘤杂交细胞中环磷酸腺苷积累的增强作用。

J Biol Chem. 1981 Jul 10;256(13):6573-6.

Polyamines and cellular adenosine 3' :5'-cyclic monophosphate.多胺与细胞3',5'-环磷酸腺苷

Biochem J. 1979 Sep 15;182(3):641-9. doi: 10.1042/bj1820641a.

Enkephalin dimers: regulation of cyclic AMP levels in NG108-15 cells.

Life Sci. 1983 Jan 31;32(5):511-6. doi: 10.1016/0024-3205(83)90145-5.

Irreversible inactivation of the opiate receptors in the neuroblastoma x glioma hybrid NG108-15 by chlornaltrexamine.

Mol Pharmacol. 1981 Jul;20(1):8-15.

Regulation by neurohormones of cyclic AMP concentration in cells derived from the nervous system.神经激素对源自神经系统的细胞中环磷酸腺苷浓度的调节。

Adv Cyclic Nucleotide Res. 1981;14:637-45.

引用本文的文献

The opiate receptors.

Neurochem Res. 1976 Feb;1(1):3-28. doi: 10.1007/BF00965627.

Inhibition by morphine of prostaglandin E1-stimulated secretion and cyclic adenosine 3',5'-monophosphate formation in the rat jejunum in vivo.吗啡对大鼠空肠中前列腺素E1刺激的分泌及环磷酸腺苷生成的体内抑制作用。

Br J Pharmacol. 1980 Mar;68(3):513-8. doi: 10.1111/j.1476-5381.1980.tb14566.x.

Cluster formation of opiate (enkephalin) receptors in neuroblastoma cells: differences between agonists and antagonists and possible relationships to biological functions.神经母细胞瘤细胞中阿片样物质（脑啡肽）受体的簇集形成：激动剂与拮抗剂之间的差异以及与生物学功能的可能关系。

Proc Natl Acad Sci U S A. 1980 May;77(5):3038-41. doi: 10.1073/pnas.77.5.3038.

Inhibition of stimulated fluid secretion in the rat small and large intestine by opiate agonists.阿片类激动剂对大鼠小肠和大肠中刺激引起的液体分泌的抑制作用。

Naunyn Schmiedebergs Arch Pharmacol. 1979 Mar;306(2):113-8. doi: 10.1007/BF00498980.

Regulation of acetylcholine release from neuroblastoma x glioma hybrid cells.神经母细胞瘤与胶质瘤杂交细胞中乙酰胆碱释放的调节

Proc Natl Acad Sci U S A. 1978 Mar;75(3):1314-8. doi: 10.1073/pnas.75.3.1314.

Interactions of opiates and prostaglandins E with regard to cyclic AMP in striatal tissue of rats in vitro.阿片类药物与前列腺素E在体外大鼠纹状体组织中对环磷酸腺苷的相互作用。

Naunyn Schmiedebergs Arch Pharmacol. 1978 Mar;302(1):103-6. doi: 10.1007/BF00586604.

Urinary cyclic AMP excretion by methadone subjects during gradual and acute withdrawal.美沙酮治疗患者在逐渐脱毒和急性脱毒期间尿中环磷酸腺苷的排泄情况。

Psychopharmacology (Berl). 1977 Aug 31;54(1):17-20. doi: 10.1007/BF00426534.

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