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度洛西汀的疗效取决于神经性疼痛模型大鼠的脊髓胆碱能可塑性。

The efficacy of duloxetine depends on spinal cholinergic plasticity in neuropathic pain model rats.

作者信息

Kato Daiki, Suto Takashi, Obata Hideaki, Saito Shigeru

机构信息

Department of Anesthesiology, Gunma University Graduate School of Medicine, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan.

Department of Anesthesiology, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama 350-8550, Japan.

出版信息

IBRO Neurosci Rep. 2022 Feb 12;12:188-196. doi: 10.1016/j.ibneur.2022.02.004. eCollection 2022 Jun.

Abstract

Antidepressants, such as duloxetine, are widely used to treat chronic pain, including neuropathic pain; however, their efficacy is unsatisfactory. In our previous studies, we showed that in a spinal nerve ligation (SNL) rat model, the descending noradrenergic inhibitory system, which involves in the anti-hypersensitivity mechanism of antidepressants, decrease its activity over time following peripheral nerve injury. In this study, we hypothesized that the analgesic effects of duloxetine may diminish following the attenuation of the descending noradrenergic inhibitory system. The analgesic effects of duloxetine in SNL model rats at the early (SNL2W) and chronic (SNL6W) phases following spinal nerve ligation were compared. Male Sprague-Dawley rats were randomly assigned to the SNL2W or SNL6W groups and used to evaluate the anti-allodynic effects of duloxetine using the von Frey filament test. The anti-allodynic effects of duloxetine at a dose of 10 mg/kg were lower in SNL6W rats than in SNL2W rats. Basal noradrenaline concentrations in rat spinal dorsal horns were higher in the SNL6W group than in the SNL2W group, and there was no difference in the increase in spinal noradrenaline concentrations between the 2 groups following duloxetine administration. In addition, we found that duloxetine-induced acetylcholine (ACh) release and choline acetyltransferase (ChAT) expression in the spinal dorsal horn decreased in SNL6W rats. At a dose of 30 mg/kg, duloxetine showed anti-allodynic effects even in SNL6W rats and induced ACh release in the spinal cord. Furthermore, these anti-allodynic effects were completely inhibited by intrathecal atropine (muscarinic antagonist) administration. Moreover, 5 daily intraperitoneal injections of the TrkB agonist, 7,8-dihydroxyflavone (5 mg/kg), not only restored ChAT expression, but also decreased the anti-allodynic effects of duloxetine. These findings suggest that the attenuation of the anti-allodynic effects of duloxetine at the chronic phase of SNL may be due to impaired spinal acetylcholine-mediated analgesia. In addition, the activation of BDNF-TrkB signaling may be beneficial in reversing this impairment.

摘要

抗抑郁药,如度洛西汀,被广泛用于治疗慢性疼痛,包括神经性疼痛;然而,其疗效并不理想。在我们之前的研究中,我们表明,在脊髓神经结扎(SNL)大鼠模型中,参与抗抑郁药抗超敏反应机制的下行去甲肾上腺素能抑制系统,在周围神经损伤后会随着时间的推移而降低其活性。在本研究中,我们假设度洛西汀的镇痛作用可能会随着下行去甲肾上腺素能抑制系统的减弱而减弱。比较了度洛西汀在脊髓神经结扎后的早期(SNL2W)和慢性期(SNL6W)对SNL模型大鼠的镇痛作用。将雄性Sprague-Dawley大鼠随机分为SNL2W或SNL6W组,并使用von Frey细丝试验来评估度洛西汀的抗痛觉过敏作用。在SNL6W大鼠中,10mg/kg剂量的度洛西汀的抗痛觉过敏作用低于SNL2W大鼠。SNL6W组大鼠脊髓背角中的基础去甲肾上腺素浓度高于SNL2W组,且两组在给予度洛西汀后脊髓去甲肾上腺素浓度的增加没有差异。此外,我们发现度洛西汀诱导的脊髓背角乙酰胆碱(ACh)释放和胆碱乙酰转移酶(ChAT)表达在SNL6W大鼠中降低。在30mg/kg剂量下,度洛西汀即使在SNL6W大鼠中也显示出抗痛觉过敏作用,并诱导脊髓中ACh释放。此外,鞘内注射阿托品(毒蕈碱拮抗剂)可完全抑制这些抗痛觉过敏作用。此外,每天腹腔注射5次TrkB激动剂7,8-二羟基黄酮(5mg/kg),不仅恢复了ChAT表达,还降低了度洛西汀的抗痛觉过敏作用。这些发现表明,度洛西汀在SNL慢性期抗痛觉过敏作用的减弱可能是由于脊髓乙酰胆碱介导的镇痛作用受损。此外,BDNF-TrkB信号的激活可能有助于逆转这种损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3198/8881419/5a464fced8b1/gr1.jpg

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