Tuross N, Patrick R L
J Pharmacol Exp Ther. 1986 Jun;237(3):739-45.
These studies were undertaken to determine the effects of propranolol on catecholamine synthesis and uptake in the rat central nervous system. The effects of propranolol on catecholamine synthesis were studied in vitro in striatal and hypothalamic synaptosomes, and also in vivo. In addition, the effects of propranolol on catecholamine uptake in striatal and hypothalamic synaptosomes were evaluated. Propranolol inhibited synaptosomal catecholamine synthesis and uptake in both tissues. Norepinephrine uptake in the hypothalamus was most sensitive to propranolol inhibition (IC50 = 5 microM). Dopamine synthesis in striatal synaptosomes was also inhibited markedly, with an IC50 = 8 microM. After in vivo administration, propranolol decreased the accumulation of dopa in the striatum, confirming propranolol's synthesis inhibiting effect in dopaminergic terminals. Studies of soluble striatal tyrosine hydroxylase revealed that propranolol has a direct inhibitory effect on the enzyme. These results indicate that propranolol administration may cause a potentiation of norepinephrine activity specifically at alpha receptors, due to concurrent beta receptor blockade and inhibition of norepinephrine reuptake and a decrease in dopamine activity at dopaminergic receptor sites due to an inhibition of dopamine formation.
开展这些研究以确定普萘洛尔对大鼠中枢神经系统中儿茶酚胺合成及摄取的影响。在体外对纹状体和下丘脑突触体以及在体内研究了普萘洛尔对儿茶酚胺合成的影响。此外,还评估了普萘洛尔对纹状体和下丘脑突触体中儿茶酚胺摄取的影响。普萘洛尔抑制了这两种组织中突触体的儿茶酚胺合成及摄取。下丘脑中去甲肾上腺素的摄取对普萘洛尔抑制最为敏感(半数抑制浓度[IC50]=5微摩尔)。纹状体突触体中的多巴胺合成也受到显著抑制,IC50=8微摩尔。体内给药后,普萘洛尔降低了纹状体中多巴的蓄积,证实了普萘洛尔在多巴胺能终末的合成抑制作用。对可溶性纹状体酪氨酸羟化酶的研究表明,普萘洛尔对该酶有直接抑制作用。这些结果表明,由于同时存在β受体阻断以及去甲肾上腺素再摄取抑制,普萘洛尔给药可能会导致去甲肾上腺素活性在α受体处特异性增强,并且由于多巴胺生成受到抑制,多巴胺能受体部位的多巴胺活性降低。