Kanig K, Tencheva Z S, Nitschki J, Dingler W H
Arzneimittelforschung. 1976;26(12):2155-8.
Beta-Dimethylaminoethyl-p-chlorophenoxyacetate hydrochloride (meclofenoxate, Helfergin) was adminstered orally in dosages of 300 mg/kg 3 times during an 18-h period. The incorporation rate of the total and cytoplasmic RNA as well as of ATP, ADP and AMP decreased. Contradictory results were obtained after a 16-day treatment with orally 300 mg/kg per day: while the 32P-incorporation rate of the cytoplasmic RNA and the 3 adenosine phosphates increased, the nuclear RNA showed a correspondent diminishing. No changes of the ATP content could be observed in any group. The differences between the acute and chronic experiments could be explained by a different excitation of the animals and by the very different dosages. The increased 32P-incorporation into the cytoplasmic and into the adenosine phosphates in the chronic experiments are explained by a stimulation of the pentose phosphate shunt which yields mainly the phosphate group for the synthesis of AMP.
盐酸β - 二甲基氨基乙基 - 对氯苯氧基乙酸酯(氯酯醒,海弗金)在18小时内分3次口服给药,剂量为300毫克/千克。总RNA、细胞质RNA以及ATP、ADP和AMP的掺入率均下降。每天口服300毫克/千克,治疗16天后得到了相互矛盾的结果:虽然细胞质RNA和3种腺苷磷酸的32P掺入率增加,但核RNA却相应减少。任何组均未观察到ATP含量的变化。急性和慢性实验之间的差异可以通过动物的不同兴奋状态和非常不同的剂量来解释。慢性实验中细胞质和腺苷磷酸中32P掺入增加是由于磷酸戊糖途径的刺激,该途径主要产生用于合成AMP的磷酸基团。