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肾上腺素能刺激和阻断后大鼠胃黏膜中的环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)

Rat gastric mucosal cAMP and cGMP after adrenergic stimulation and blockade.

作者信息

Ruoff H J

出版信息

Eur J Pharmacol. 1977 Aug 15;44(4):349-54. doi: 10.1016/0014-2999(77)90309-0.

Abstract

The effect of adrenergic stimulation and blockade on the concentration of cAMP and cGMP was studied in the rat gastric mucosa. Adrenaline (0.5-2.0 mg/kg) elevated the gastric mucosal cAMP and cGMP levels up to 100% in a dose-dependent manner. Blockade of the beta-adrenoceptors with 4 mg/kg propranolol suppressed the adrenaline effect on the cAMP level and increased the effect on the cGMP concentration up to 500%. The opposite effect was found under alpha-adrenoceptor blockade. Phenoxybenzamine, 4 mg/kg, prevented the adrenaline effect on the cGMP level and increased the effect on the cAMP concentration up to 300%. Predominant stimulation of the beta-adrenoceptors by isoproterenol or of the alpha-adrenoceptors by phenylephrine caused smaller changes in the cyclic nucleotide concentration than did adrenaline. Their effect was more pronounced when the non-stimulated receptor was blocked. The data indicate that the rat gastric mucosa contains alpha- and beta-adrenoceptors. The effect of adrenaline on the gastric mucosal cAMP level is mediated by beta-adrenoceptors and that on the cGMP level by alpha-adrenoceptors.

摘要

在大鼠胃黏膜中研究了肾上腺素能刺激和阻断对环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)浓度的影响。肾上腺素(0.5 - 2.0毫克/千克)以剂量依赖的方式使胃黏膜cAMP和cGMP水平升高达100%。用4毫克/千克普萘洛尔阻断β - 肾上腺素能受体可抑制肾上腺素对cAMP水平的作用,并使对cGMP浓度的作用增加达500%。在α - 肾上腺素能受体阻断时发现了相反的效果。4毫克/千克的酚苄明可阻止肾上腺素对cGMP水平的作用,并使对cAMP浓度的作用增加达300%。异丙肾上腺素对β - 肾上腺素能受体的主要刺激或去氧肾上腺素对α - 肾上腺素能受体的刺激所引起的环核苷酸浓度变化比肾上腺素小。当未受刺激的受体被阻断时,它们的作用更明显。数据表明大鼠胃黏膜含有α和β肾上腺素能受体。肾上腺素对胃黏膜cAMP水平的作用由β - 肾上腺素能受体介导,而对cGMP水平的作用由α - 肾上腺素能受体介导。

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