Gardner D G, Brown E M, Aurbach G D
Endocrinology. 1979 Aug;105(2):360-6. doi: 10.1210/endo-105-2-360.
Sodium nitroprusside effected a significant reduction in intracellular cAMP accumulation and parathyroid hormone release in dispersed bovine parathyroid cells. The inhibition was apparent at 3 x 10-4 M and maximal at 10-2 M nitroprusside. The effect was rapid and reversible and could be demonstrated in both the presence and absence of stimulating agonists [i.e. (-)isoproterenol, dopamine, and cholera toxin]. The inhibition was additive with that previously described for alpha-adrenergic agonists and prostaglandin F2 alpha and was not affected by phentolamine, suggesting that nitroprusside does not act through the inhibitory receptors previously described in this system. The nitroprusside effect on cAMP accumulation and parathyroid hormone release was present at virtually all concentrations of extracellular calcium tested; 2mM EGTA failed to prevent the inhibition. While extracellular calcium may play some role in this inhibition, it is not required for demonstration of the effect.
硝普钠可使分散的牛甲状旁腺细胞内的环磷酸腺苷(cAMP)积累和甲状旁腺激素释放显著减少。在硝普钠浓度为3×10⁻⁴M时抑制作用明显,在10⁻²M时达到最大抑制效果。该作用迅速且可逆,在有或没有刺激激动剂[即(-)异丙肾上腺素、多巴胺和霍乱毒素]的情况下均可表现出来。这种抑制作用与先前描述的α-肾上腺素能激动剂和前列腺素F2α的抑制作用具有相加性,且不受酚妥拉明影响,这表明硝普钠并非通过该系统中先前描述的抑制性受体起作用。在几乎所有测试的细胞外钙浓度下,硝普钠对cAMP积累和甲状旁腺激素释放均有作用;2mM的乙二醇双(2-氨基乙醚)四乙酸(EGTA)未能阻止这种抑制作用。虽然细胞外钙可能在这种抑制中起一定作用,但该作用的表现并不依赖于细胞外钙。