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吗啡诱导大鼠尾状核胆碱乙酰转移酶的动力学改变。

Morphine-induced kinetic alterations of choline acetyltransferase of the rat caudate nucleus.

作者信息

Datta K, Wajda I J

出版信息

Br J Pharmacol. 1972 Apr;44(4):732-41. doi: 10.1111/j.1476-5381.1972.tb07311.x.

Abstract
  1. In order to explain the decrease of choline acetyltransferase (2.3.1.6.) activity observed in the caudate nucleus of morphine-treated rats, partially purified preparations of the enzyme were used in kinetic studies, with choline as substrate.2. The apparent Michaelis constant for the enzyme obtained from normal rats was found to be 0.9 mM choline; this value doubled when the animals were killed one hour after a single injection of morphine (30 mg/kg). When the rats were injected daily for 4 or 15 days, and killed one hour after the last injection, the apparent Km value was 2.1 mM in each case. Prolonged daily treatment with morphine, followed by 48 h withdrawal, or by administration of 4 mg/kg of naloxone (given half an hour after the last injection of morphine) resulted in apparent Km values of 1.3-1.5 mM of choline, suggesting a gradual return to the lower, normal substrate requirement. Vmax changes were insignificant.3. The effect of morphine added in vitro to different enzyme preparations was also studied. The Km values of 0.9 mM, in the enzyme isolated from normal rats, increased to 2.0 after incubation in vitro with 12.5 mM morphine. Similar increases were found in enzymes obtained from rats 48 h after the withdrawal of morphine or from rats injected with naloxone after prolonged morphine treatment. The high apparent Km values, found in enzyme obtained from animals killed one hour after the last dose of morphine, did not change upon incubation with 12.5 mM morphine. A similar pattern of Km changes was noticed after incubation with 25 mM acetylcholine.4. An increase of 32% in acetylcholine (ACh) level was found in the caudate nucleus one hour after subcutaneous injection of 30 mg/kg of morphine. Return to normal values was observed when morphine was administered daily. After two to three weeks of daily treatment and subsequent withdrawal from morphine for 48 h, the levels of ACh were normal. If the daily treated rats were given naloxone within half an hour of the last injection of morphine, and killed 30 min later, the levels of ACh remained normal.5. Fifty per cent inhibition of enzyme activity was observed upon in vitro incubation with 75 mM acetylcholine, or with 25 mM morphine. The same degree of inhibition was noticed when the enzyme was obtained from normal or from morphine-treated rats.
摘要
  1. 为了解释在吗啡处理的大鼠尾状核中观察到的胆碱乙酰转移酶(2.3.1.6.)活性降低的现象,在动力学研究中使用了部分纯化的该酶制剂,以胆碱作为底物。

  2. 从正常大鼠获得的该酶的表观米氏常数被发现为0.9 mM胆碱;当动物在单次注射吗啡(30 mg/kg)后1小时处死时,该值翻倍。当大鼠每日注射4天或15天,并在最后一次注射后1小时处死时,每种情况下的表观Km值均为2.1 mM。长期每日用吗啡治疗,随后停药48小时,或在最后一次注射吗啡后半小时给予4 mg/kg纳洛酮,导致胆碱的表观Km值为1.3 - 1.5 mM,表明逐渐恢复到较低的正常底物需求。Vmax变化不显著。

  3. 还研究了体外向不同酶制剂中添加吗啡的效果。从正常大鼠分离的酶的Km值为0.9 mM,在体外与12.5 mM吗啡孵育后增加到2.0。在吗啡撤药48小时后的大鼠或长期吗啡治疗后注射纳洛酮的大鼠获得的酶中也发现了类似的增加。在最后一剂吗啡后1小时处死的动物获得的酶中发现的高表观Km值,在与12.5 mM吗啡孵育后没有变化。与25 mM乙酰胆碱孵育后也观察到类似的Km变化模式。

  4. 皮下注射30 mg/kg吗啡后1小时,尾状核中的乙酰胆碱(ACh)水平增加了32%。每日给予吗啡时观察到恢复到正常值。在每日治疗两到三周并随后停用吗啡48小时后,ACh水平正常。如果在最后一次注射吗啡后半小时内给每日治疗的大鼠注射纳洛酮,并在30分钟后处死,ACh水平保持正常。

  5. 在体外与75 mM乙酰胆碱或25 mM吗啡孵育时观察到酶活性有50%的抑制。当酶从正常大鼠或吗啡处理的大鼠获得时,观察到相同程度的抑制。

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本文引用的文献

4
Drug-induced changes in brain acetylcholine.药物引起的大脑乙酰胆碱变化。
Br J Pharmacol Chemother. 1962 Oct;19(2):226-34. doi: 10.1111/j.1476-5381.1962.tb01184.x.

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