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将AMPA或一种代谢型谷氨酸受体激动剂反复注射到大鼠腹侧被盖区,会增强随后由可卡因诱导的行为多动。

Repeated administration of AMPA or a metabotropic glutamate receptor agonist into the rat ventral tegmental area augments the subsequent behavioral hyperactivity induced by cocaine.

作者信息

Dunn Justin M, Inderwies Brian R, Licata Stephanie C, Pierce R Christopher

机构信息

Laboratory of Neuropsychopharmacology, Department of Pharmacology, Boston University School of Medicine, 715 Albany Street, Boston, MA, 02118, USA.

出版信息

Psychopharmacology (Berl). 2005 Apr;179(1):172-80. doi: 10.1007/s00213-004-2054-9. Epub 2004 Dec 4.

Abstract

RATIONALE

Glutamate receptors and their related second messengers in the ventral tegmental area (VTA) are known to play critical roles in the initiation of behavioral sensitization to cocaine.

OBJECTIVES

To evaluate the hypothesis that repeated intra-VTA microinjections of the ionotropic glutamate agonist, AMPA, or the metabotropic glutamate agonist, t-ACPD, augment the behavioral hyperactivity induced by a subsequent challenge injection of cocaine. In addition, the dependency of the t-ACPD effect on activation of the calcium/calmodulin-dependent kinases (CaM-Ks) was assessed.

METHODS

Male Sprague-Dawley rats received four once-daily microinjections of saline, AMPA, t-ACPD, or t-ACPD plus the CaM-KII inhibitor KN-93 directly into the VTA; locomotor activity was measured for 120 min after each of the daily treatments. One week after the 4 treatment days, all animals received a challenge injection of cocaine (15 mg/kg, IP) and behavioral activity was monitored for 120 min.

RESULTS

Intra-VTA administration of t-ACPD increased behavioral activity only on the first 2 treatment days, an effect that was blocked by pre-treatment with KN-93. Administration of AMPA into the VTA, in contrast, produced behavioral hyperactivity that sensitized over the 4 treatment days. Following the cocaine challenge injection, there was an augmentation of cocaine-induced behavioral hyperactivity in the groups pretreated with AMPA or t-ACPD but not in the animals administered t-ACPD plus KN-93.

CONCLUSIONS

These results indicate that repeated stimulation of AMPA or metabotropic glutamate receptors in the VTA mimics the initiation of behavioral sensitization to cocaine. The present findings also suggest that glutamate agonist-induced activation of CaM-KII in the VTA plays a critical role in the behavioral and neuronal plasticity induced by repeated cocaine injections.

摘要

理论依据

已知腹侧被盖区(VTA)中的谷氨酸受体及其相关的第二信使在对可卡因行为敏化的起始过程中起关键作用。

目的

评估以下假设,即向VTA内反复微量注射离子型谷氨酸受体激动剂AMPA或代谢型谷氨酸受体激动剂t-ACPD,会增强随后一次注射可卡因所诱发的行为多动。此外,还评估了t-ACPD效应对钙/钙调蛋白依赖性激酶(CaM-Ks)激活的依赖性。

方法

雄性Sprague-Dawley大鼠每天一次接受向VTA内直接微量注射生理盐水、AMPA、t-ACPD或t-ACPD加CaM-KII抑制剂KN-93,共4次;每次每日处理后测量120分钟的运动活性。在4个处理日之后的一周,所有动物接受一次可卡因(15mg/kg,腹腔注射)激发注射,并监测120分钟的行为活性。

结果

向VTA内注射t-ACPD仅在最初2个处理日增加行为活性,该效应被KN-93预处理所阻断。相比之下,向VTA内注射AMPA产生的行为多动在4个处理日内出现敏化。在可卡因激发注射后,预先用AMPA或t-ACPD处理的组中可卡因诱发的行为多动增强,但在给予t-ACPD加KN-93的动物中未增强。

结论

这些结果表明,VTA中AMPA或代谢型谷氨酸受体的反复刺激模拟了对可卡因行为敏化的起始。目前的研究结果还表明,谷氨酸受体激动剂诱导的VTA中CaM-KII的激活在反复注射可卡因所诱导的行为和神经元可塑性中起关键作用。

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