胆碱能、肾上腺素能和PGE1对环核苷酸和培养角膜上皮生长的影响。

H D Cavanagh, A M Colley
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摘要

观察肾上腺素能、胆碱能药物和前列腺素E1对角膜上皮细胞环核苷酸积累、生长参数和基底膜合成的影响。8-溴-cGMP显著(p < 0.05)促进了标记胸苷和亮氨酸的掺入,乙酰胆碱和氨甲酰胆碱也显著(p < 0.05)提高了cGMP,降低了cAMP/cGMP比值。对乙酰胆碱的反应被阿托品和-班加罗毒素所消除。二丁基cAMP和5′-单磷酸腺苷以及去甲肾上腺素、肾上腺素、前列腺素E1和茶碱均能抑制前体掺入,显著升高cAMP水平和cAMP/cGMP比值。心得安,而非苯氧苄胺,能阻断对有效浓度去甲肾上腺素的反应。去甲肾上腺素、PGE1和二丁基cAMP也显著提高了标记葡萄糖胺的摄取和标记脯氨酸进入胶原酶敏感蛋白或蛋白水解物的羟脯氨酸部分,而乙酰胆碱对基底膜合成的参数没有影响。心得安阻断对去甲肾上腺素的反应。结果与cgmp介导的胆碱能递质在角膜上皮生长调节中的刺激作用一致,camp介导的β -肾上腺素能抑制角膜上皮初始损伤后的再生和基底膜生成的增加,以及前列腺素增强肾上腺素能的作用。
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Cholinergic, adrenergic, and PGE1 effects on cyclic nucleotides and growth in cultured corneal epithelium.

Effects of adrenergic and cholinergic drugs and prostaglandin E1 on cyclic nucleotide accumulation and parameters of growth and basement membrane synthesis were examined in corneal epithelial cell cultures. 8-bromo-cGMP significantly (p less than 0.05) enhanced incorporation of labeled thymidine and leucine, as did acetylcholine and carbamylcholine, which elevated cGMP and decreased cAMP/cGMP ratio. Responses to acetylcholine were abolished by atropine and alpha-bungarotoxin. Precursor incorporation was inhibited by dibutyryl cAMP and adenosine 5'-monophosphate and by norepinephrine, epinephrine, prostaglandin E1, and theophylline, which significantly elevated cAMP levels and cAMP/cGMP ratio. Propranolol, but not phenoxybenzamine, blocked responses to effective concentrations of norepinephrine. Norepinephrine, PGE1, and dibutyryl cAMP also significantly elevated uptake of labeled glucosamine and incorporation of labeled proline into collagenase-sensitive protein or the hydroxyproline fraction of protein hydrolysates, while acetylcholine had no effect on parameters of basement membrane synthesis. Propranolol blocked responses to norepinephrine. Results were consistent with a cGMP-mediated stimulatory role of the cholinergic transmitter in corneal epithelial growth regulation, cAMP-mediated beta-adrenergic suppression of regrowth and increased basement membrane production after initial injury to the corneal epithelium, and potentiation of the adrenergic effect by prostaglandins.

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