Gutman Y, Boonyaviroj P
J Neural Transm. 1977;40(4):245-52. doi: 10.1007/BF01257018.
In rat adrenal gland incubated in vitro, phenylephrine and naphazoline inhibited the release of catecholamines (CA) induced in a medium containing K+ (5.6mM). In K+-free medium or in the presence of ouabain (10(-3) M) phenylephrine and naphazoline had no effect on CA release. The alpha-adrenergic blockers, phentolamine and phenoxybenzamine, increased CA release in a K+-medium but had no effect on CA release from adrenal medulla in a K+-free or ouabain (10(-3) M) containing medium. PGE2 inhibited the release of CA both in the presence and in the absence of K+, as well as in the presence of ouabain (10(-3) M). Activation of alpha-adrenergic receptors in the adrenal medulla by phenylephrine and naphazoline resulted in increased Na, K-ATPase activity but no effect on Mg-ATPase. PGE2 acts through a different mechanism.
在体外培养的大鼠肾上腺中,去氧肾上腺素和萘甲唑啉抑制在含5.6mM钾离子的培养基中诱导的儿茶酚胺(CA)释放。在无钾离子培养基中或存在哇巴因(10⁻³M)时,去氧肾上腺素和萘甲唑啉对CA释放无影响。α-肾上腺素能阻滞剂酚妥拉明和酚苄明在含钾离子培养基中增加CA释放,但在无钾离子或含哇巴因(10⁻³M)的培养基中对肾上腺髓质CA释放无影响。前列腺素E2在有钾离子和无钾离子存在时以及在有哇巴因(10⁻³M)存在时均抑制CA释放。去氧肾上腺素和萘甲唑啉激活肾上腺髓质中的α-肾上腺素能受体导致钠钾ATP酶活性增加,但对镁ATP酶无影响。前列腺素E2通过不同机制起作用。