首页> 外文期刊>Cerebral cortex >The cannabinoid receptor agonist WIN 55,212-2 regulates glutamate transmission in rat cerebral cortex: an in vivo and in vitro study.
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The cannabinoid receptor agonist WIN 55,212-2 regulates glutamate transmission in rat cerebral cortex: an in vivo and in vitro study.

机译:大麻素受体激动剂WIN 55,212-2调节大鼠大脑皮质中谷氨酸的传递:一项体内和体外研究。

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摘要

The effects of the cannabinoid receptor agonist WIN 55,212-2 on endogenous extracellular glutamate levels in the prefrontal cortex of the awake rat and in primary cultures of rat cerebral cortex neurons were investigated. In the prefrontal cortex WIN 55,212-2 (0.1 and 1 mg/kg i.p.) increased dialysate glutamate levels from of the awake rat, while the lower (0.01 mg/kg) and the higher (2 mg/kg) doses were ineffective. Furthermore, the WIN 55,212-2 (0.1 mg/kg)- induced increase of dialysate glutamate levels was counteracted by pretreatment with the selective CB(1) receptor antagonist SR141716A (0.1 mg/kg i.p.) and by the local perfusion with a low-calcium Ringer solution (Ca(2+) 0.2 mM). In primary cultures of rat cerebral cortex neurons, WIN 55,212-2 (0.01--100 nM) increased extracellular glutamate levels, displaying a bell-shaped concentration-response curve. The facilitatory effect of WIN 55,212-2 (1 nM) was fully counteracted by SR141716A (10 nM), by the replacement of the normal Krebs Ringer-bicarbonate buffer with a low Ca(2+) medium (0.2 mM) and by the IP(3) receptor antagonist xestospongin C (1 microM). These in vivo and in vitro findings suggest an increase in cortical glutamatergic transmission by CB(1) receptors, an effect that may underlie some of the psychoactive and behavioural actions of acute exposure to marijuana.
机译:研究了大麻素受体激动剂WIN 55,212-2对清醒大鼠前额叶皮层和大鼠大脑皮层神经元原代培养物中内源性细胞外谷氨酸水平的影响。在前额叶皮质WIN 55,212-2(0.1和1 mg / kg i.p.)使清醒大鼠的谷氨酸透析液水平增加,而较低(0.01 mg / kg)和较高(2 mg / kg)的剂量无效。此外,用选择性CB(1)受体拮抗剂SR141716A(0.1 mg / kg ip)预处理和低剂量局部灌注可抵消WIN 55,212-2(0.1 mg / kg)诱导的谷氨酸透析液水平的升高。钙林格溶液(Ca(2+)0.2 mM)。在大鼠大脑皮层神经元的原代培养中,WIN 55,212-2(0.01--100 nM)增加了细胞外谷氨酸水平,显示出钟形的浓度-反应曲线。 SR141716A(10 nM)完全抵消了WIN 55,212-2(1 nM)的促进作用,方法是用低Ca(2+)培养基(0.2 mM)代替普通的Krebs Ringer-碳酸氢盐缓冲液(IP) (3)受体拮抗剂xestospongin C(1 microM)。这些体内和体外研究结果表明,CB(1)受体可增加皮质谷氨酸能传递,这种作用可能是急性暴露于大麻的某些心理和行为行为的基础。

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