首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Dizocilpine infusion has a different effect in the development of morphine and cocaine sensitization: behavioral and neurochemical aspects.
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Dizocilpine infusion has a different effect in the development of morphine and cocaine sensitization: behavioral and neurochemical aspects.

机译:地佐西平输注在吗啡和可卡因敏化的发展中具有不同的作用:行为和神经化学方面。

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摘要

The stimulation of glutamate receptors plays a relevant role in the development of behavioral sensitization to psychostimulants, while less clear results have been obtained on their role in morphine sensitization. We addressed this issue by comparing the development of cocaine and morphine sensitization under a continuous s.c. infusion of the N-methyl-D-aspartate (NMDA) antagonist dizocilpine (0.1 mg/kg/24 h). Moreover, we studied the expression of NMDA and alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate (AMPA) receptor subunits in discrete limbic areas of rats sensitized to morphine or cocaine with or without the concomitant dizocilpine infusion. It was observed that dizocilpine infusion did not prevent the development of morphine sensitization, while it prevented the development of tolerance to morphine-induced analgesia. Finally, morphine-sensitized animals did not present any modification in the subunit expression of glutamate receptors in the brain areas examined. In agreement with previous results, we found that dizocilpine infusion prevented the development of cocaine sensitization. Moreover, we observed that rats sensitized to cocaine presented a significant increase in the levels of GLUR1, NR1 and NR2B, in the nucleus accumbens, and of NR2B in the hippocampus compared to control animals. Such modifications were absent in rats administered cocaine under dizocilpine infusion.We conclude that: (i) morphine sensitization is a neuroadaptive phenomenon which does not appear to require NMDA receptor activity in order to develop; (ii) cocaine sensitization is clearly dependent on NMDA receptor activity, as dizocilpine infusion prevented the occurrence of glutamate receptors modifications as well as the development of sensitization.
机译:谷氨酸受体的刺激在对精神兴奋剂的行为敏化的发展中起着相关的作用,而关于吗啡敏化的作用还不清楚。我们通过在连续s.c.下比较可卡因和吗啡敏化的发展来解决这个问题。输注N-甲基-D-天冬氨酸(NMDA)拮抗剂地佐西平(0.1 mg / kg / 24 h)。此外,我们研究了对吗啡或可卡因敏感的大鼠离散边缘区域中NMDA和α-氨基-3-羟基-5-甲基异恶唑-4-丙酸酯(AMPA)受体亚单位的表达,无论是否伴有地佐西平输注。观察到地佐西平输注并不能阻止吗啡致敏作用的发展,而阻止了对吗啡引起的镇痛耐受性的发展。最后,吗啡致敏动物在所检查的大脑区域中谷氨酸受体的亚基表达没有任何改变。与以前的结果一致,我们发现双佐西平输注阻止了可卡因致敏的发展。此外,我们观察到,对可卡因敏感的大鼠与对照组相比,伏隔核中的GLUR1,NR1和NR2B和海马中的NR2B的含量均显着增加。结论:(i)吗啡致敏是一种神经适应性现象,似乎不需要NMDA受体活性才能发育;(i)吗啡致敏是一种神经适应性现象。 (ii)可卡因的致敏作用显然取决于NMDA受体的活性,因为双佐西平的输注阻止了谷氨酸受体修饰的发生以及致敏作用的发展。

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