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μ 1- and 5-HT 1-dependent mechanisms in the anterior pretectal nucleus mediate the antinociceptive effects of retrosplenial cortex stimulation in rats

机译:鹰嘴前前核中的μ1-和5-HT 1依赖性机制介导大鼠脊髓后皮质刺激的镇痛作用

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Aim: This study examines if injection of cobalt chloride (CoCl 2) or antagonists of muscarinic cholinergic (atropine), μ 1-opioid (naloxonazine) or 5-HT 1 serotonergic (methiothepin) receptors into the dorsal or ventral portions of the anterior pretectal nucleus (APtN) alters the antinociceptive effects of stimulating the retrosplenial cortex (RSC) in rats. Main method: Changes in the nociceptive threshold were evaluated using the tail flick or incision pain tests in rats that were electrically stimulated at the RSC after the injection of saline, CoCl 2 (1 mM, 0.10 μL) or antagonists into the dorsal or ventral APtN. Key findings: The injection of CoCl 2, naloxonazine (5 μg/0.10 μL) or methiothepin (3 μg/0.10 μL) into the dorsal APtN reduced the stimulation-produced antinociception from the RSC in the rat tail flick test. Reduction of incision pain was observed following stimulation of the RSC after the injection of the same substances into the ventral APtN. The injection of atropine (10 ng/0.10 μL) or ketanserine (5 μg/0.10 μL) into the dorsal or ventral APtN was ineffective against the antinociception resulting from RSC stimulation. Significance: μ 1-opioid- and 5-HT 1-expressing neurons and cell processes in dorsal and ventral APtN are both implicated in the mediation of stimulation-produced antinociception from the RSC in the rat tail flick and incision pain tests, respectively.
机译:目的:这项研究检查了是否将氯化钴(CoCl 2)或毒蕈碱胆碱能(阿托品),μ1-阿片类药物(纳洛酮嗪)或5-HT 1血清能(甲氧西平)的拮抗剂注射到前直肠前部的背侧或腹侧核(APtN)改变了刺激大鼠后脾皮质(RSC)的抗伤害感受作用。主要方法:在向背侧或腹侧APtN注射生理盐水,CoCl 2(1 mM,0.10μL)或拮抗剂后,在RSC进行电刺激的大鼠中,通过甩尾或切口疼痛试验评估伤害感受性阈值的变化。主要发现:在大鼠甩尾试验中,向背侧APtN中注射CoCl 2,纳洛酮嗪(5μg/ 0.10μL)或美托西平(3μg/ 0.10μL)减少了RSC刺激产生的镇痛作用。在腹侧APtN中注射相同物质后,在刺激RSC后观察到切口疼痛的减轻。向背侧或腹侧APtN中注射阿托品(10 ng / 0.10μL)或酮色林(5μg/ 0.10μL)对于RSC刺激引起的抗伤害感受无效。意义:分别在大鼠尾部甩动和切口疼痛试验中,在背侧和腹侧APtN中表达μ1阿片样物质和5-HT 1的神经元以及细胞过程均与RSC刺激产生的镇痛作用有关。

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