Bade P, Rommelspacher H, Strauss S
Naunyn Schmiedebergs Arch Pharmacol. 1977 Mar;297(2):143-7. doi: 10.1007/BF00499923.
After injection of 20 mg/kg of the monoamine oxidase inhibitor pargyline every other day up to 9 days, the activity of N-acetyltransferase (NAT) in the pineal gland of rats remained unchanged during the light-period. At the darkness, however, an increase above controls was observed. The latter effect was not affected by subchronic administration. The monoamine oxidase inhibitor activated not only the NAT but a second enzyme with different kinetic parameters. The drug levelled the circadian changes in the content of serotonin whereas noradrenaline and 5-hydroxyindole acetic acid were hardly influenced. These findings may be explained in such a way that pargyline activates the enzyme not via beta-receptors as supposed by Deguchi and Axelrod (1972a) but by an intracellular mechanism. The increased serotonin concentration might be responsible for the additional activation of the enzyme.
每隔一天注射20毫克/千克的单胺氧化酶抑制剂优降宁,持续9天,大鼠松果体中N - 乙酰转移酶(NAT)的活性在光照期保持不变。然而,在黑暗期,观察到该酶活性高于对照组。后一种效应不受亚慢性给药的影响。单胺氧化酶抑制剂不仅激活了NAT,还激活了另一种具有不同动力学参数的酶。药物使血清素含量的昼夜变化趋于平稳,而去甲肾上腺素和5 - 羟吲哚乙酸几乎未受影响。这些发现可以这样解释:优降宁不是像出木口和阿克塞尔罗德(1972a)所推测那样通过β受体激活该酶,而是通过细胞内机制。血清素浓度的升高可能是该酶额外激活的原因。