首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >The contribution of the rostral ventromedial medulla to the antinociceptive effects of systemic morphine in restrained and unrestrained rats.
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The contribution of the rostral ventromedial medulla to the antinociceptive effects of systemic morphine in restrained and unrestrained rats.

机译:在受约束和不受约束的大鼠中,延髓腹侧延髓对全身性吗啡的抗伤害感受作用的贡献。

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摘要

Although there are numerous opioid-sensitive structures in the central nervous system, the contribution of each to the analgesic effect of systemically administered morphine is controversial. One such structure is the rostral ventromedial medulla. In the present study, we tested the hypothesis that the rostral ventromedial medulla is necessary for the full expression of systemic morphine-induced antinociception. Additionally, we examined whether the modulatory effect of the rostral ventromedial medulla on tail-flick latency is dependent on the behavioral state of the animal. In unrestrained rats, inactivation of the rostral ventromedial medulla with either lidocaine (0.5 microl of 4%) or muscimol (50 ng) had no effect on tail-flick latency. In contrast, in restrained rats, inactivation of the rostral ventromedial medulla with either lidocaine (0.5 microl of 4%) or muscimol (50 ng) significantly decreased tail-flick latency. In both conditions, microinjection of morphine (5 microg) into this region significantly increased tail-flick latency. Additionally, in unrestrained rats, muscimol (50 ng) and cholecystokinin tetrapeptide (0.5 ng) infusion into the rostral ventromedial medulla completely reversed systemic morphine-induced analgesia, while lidocaine (0.5 microl of 4%) and cholecystokinin octapeptide (0.25 ng) infusion partially reversed systemic morphine-induced analgesia. These findings demonstrate that the rostral ventromedial medulla does not tonically modulate tail-flick latency in unrestrained rats, but does modulate tail-flick latency when animals are stressed via restraint. These findings also strongly support the hypothesis that the rostral ventromedial medulla is necessary for the full analgesic effects of systemically administered morphine.
机译:尽管中枢神经系统中存在许多阿片类药物敏感结构,但是每种药物对全身性吗啡镇痛作用的贡献是有争议的。一种这样的结构是延髓腹侧延髓。在本研究中,我们测试了以下假设:鼻侧腹膜延髓对于系统性吗啡诱导的抗伤害感受的完整表达是必需的。此外,我们检查了延髓腹侧延髓潜伏潜伏期的调节作用是否取决于动物的行为状态。在不受约束的大鼠中,利多卡因(0.5微升,浓度为4%)或麝香酚(50纳克)使延髓腹侧延髓失活对甩尾潜伏期没有影响。相反,在受限制的大鼠中,利多卡因(0.5微升,浓度为4%)或麝香酚(50纳克)使延髓腹侧延髓失活,可显着降低甩尾潜伏期。在两种情况下,向该区域微量注射吗啡(5微克)都会显着增加甩尾潜伏期。此外,在不受约束的大鼠中,将麝香酚(50 ng)和胆囊收缩素四肽(0.5 ng)输注到延髓腹侧延髓完全逆转了系统性吗啡诱导的镇痛作用,而利多卡因(0.5微升,占4%)和胆囊收缩素八肽(0.25 ng)输注逆转全身吗啡引起的镇痛作用。这些发现表明,在不受约束的大鼠中,延髓腹侧延髓不会在声调上调节甩尾潜伏期,但在通过约束使动物受到压力时,它会调节甩尾潜伏期。这些发现也强有力地支持了以下假设:对于全身给药吗啡的全面镇痛作用而言,延髓腹侧延髓是必需的。

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