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不可逆修饰后大鼠D2多巴胺受体作为衰老和慢性利血平治疗函数的差异恢复率:受体调节机制的关键

Differential recovery rates of rat D2 dopamine receptors as a function of aging and chronic reserpine treatment following irreversible modification: a key to receptor regulatory mechanisms.

作者信息

Norman A B, Battaglia G, Creese I

出版信息

J Neurosci. 1987 May;7(5):1484-91. doi: 10.1523/JNEUROSCI.07-05-01484.1987.

Abstract

The density of D2 dopamine receptors identified by 3H-spiperone binding was significantly lower in the striatum of senescent (28-month-old) than in mature (4-month-old) Fischer 344 rats. The time course of recovery of 3H-spiperone binding to D2 dopamine receptors following irreversible receptor modification by a single injection of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) was significantly slower in senescent than in mature rats. The kinetics of D2 dopamine receptor repopulation could be adequately described by a model assuming a constant rate of receptor production and a rate of degradation that was dependent on receptor concentration. Both the production rate and degradation rate constant of D2 dopamine receptors were lower in the senescent rats compared to mature rats. The changes in receptor density that occur as a function of development and aging are the result of changes in both the receptor production rate and receptor degradation rate constant, which, while both are reduced, tend to maintain receptor density. That is, receptor density decreased by 26% from 4 to 28 months of age, although the receptor production rate and degradation rate constant decreased by 40-50%. Chronic treatment of rats with reserpine produced a 21% increase in the density of striatal D2 dopamine receptors of mature, but not senescent, rats, accompanied by an increase in the initial recovery rate of 3H-spiperone binding sites following EEDQ treatment. It might have been expected that the reduced formation of agonist-bound receptors would have lead to a decrease in the receptor degradation rate constant.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过3H-螺哌隆结合鉴定的D2多巴胺受体密度,在衰老的(28月龄)Fischer 344大鼠纹状体中显著低于成熟的(4月龄)大鼠。单次注射N-乙氧羰基-2-乙氧基-1,2-二氢喹啉(EEDQ)对受体进行不可逆修饰后,衰老大鼠中3H-螺哌隆与D2多巴胺受体结合的恢复时间进程显著慢于成熟大鼠。D2多巴胺受体再填充的动力学可以用一个模型充分描述,该模型假设受体产生速率恒定,降解速率取决于受体浓度。与成熟大鼠相比,衰老大鼠中D2多巴胺受体的产生速率和降解速率常数均较低。作为发育和衰老函数的受体密度变化是受体产生速率和受体降解速率常数变化的结果,虽然两者都降低,但倾向于维持受体密度。也就是说,从4月龄到28月龄,受体密度下降了26%,尽管受体产生速率和降解速率常数下降了40 - 50%。用利血平对大鼠进行慢性治疗,可使成熟大鼠而非衰老大鼠纹状体D2多巴胺受体密度增加21%,同时EEDQ治疗后3H-螺哌隆结合位点的初始恢复速率增加。可能有人预期,激动剂结合受体形成减少会导致受体降解速率常数降低。(摘要截断于250字)

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