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5-HT1A 受体在光生物调节诱导的神经病理性疼痛动物模型中的镇痛作用中的中枢作用。

Central involvement of 5-HT1A receptors in antinociception induced by photobiomodulation in animal model of neuropathic pain.

机构信息

Physiotherapy Department, Federal University of Alfenas (UNIFAL), Alfenas, Brazil.

State University of Midwest Paraná - Unicentro, Guarapuava, PR, Brazil.

出版信息

Lasers Med Sci. 2022 Mar;37(2):821-829. doi: 10.1007/s10103-021-03318-w. Epub 2021 Apr 22.

DOI:10.1007/s10103-021-03318-w
PMID:33890191
Abstract

This study aimed to investigate the central involvement of 5-HT1A receptors in the nociceptive behavior of mice submitted to the chronic constriction injury (CCI) of sciatic nerve and the subsequent application of photobiomodulation (PBM). Male mice (Swiss-albino) were submitted to CCI and subsequently received an infusion of WAY100635 (5-HT1A receptor antagonist) or intracerebroventricular saline (ICV), followed by infrared laser irradiation (808 nm), in continuous mode, with the power of 100 mW and a dose of 0 J/cm (control group) or 50 J/cm. The thermal hyperalgesia was evaluated by hot plate test, while mechanical allodynia was evaluated by von Frey filaments. After CCI, animals showed a reduction in the nociceptive threshold (p<0.001) when compared to the sham group. In von Frey test, the CCI + saline + PBM 50 J/cm group showed an increase in nociceptive threshold (p<0.001) in all measurement moments in comparison with groups CCI + SALINE + PBM 0 J/cm, CCI + WAY100635 + PBM 50 J/cm, and CCI + WAY100635 + PBM 0 J/cm. Similarly, in hot plate test, CCI + SALINE + PBM 50 J/cm group showed an increase in nociceptive threshold after application of PBM at 120 and 180 min. Because of the results found, it can be suggested the involvement of 5-HT1A receptors in the central nervous system, since WAY100635 was able to reverse the antinociceptive effect provided by PBM in animals submitted to CCI.

摘要

本研究旨在探讨 5-HT1A 受体在慢性坐骨神经缩窄损伤(CCI)后小鼠痛觉行为中的中枢作用,以及随后的光生物调节(PBM)应用。雄性小鼠(瑞士白化病)接受 CCI 后,随后接受 WAY100635(5-HT1A 受体拮抗剂)或脑室生理盐水(ICV)输注,随后进行红外激光照射(808nm),连续模式,功率为 100mW,剂量为 0J/cm(对照组)或 50J/cm。热痛觉过敏通过热板试验评估,机械性痛觉过敏通过 von Frey 纤维评估。CCI 后,与假手术组相比,动物的痛觉阈值降低(p<0.001)。在 von Frey 试验中,与 CCI + SALINE + PBM 0J/cm 组、CCI + WAY100635 + PBM 50J/cm 组和 CCI + WAY100635 + PBM 0J/cm 组相比,CCI + SALINE + PBM 50J/cm 组在所有测量时刻的痛觉阈值均增加(p<0.001)。同样,在热板试验中,CCI + SALINE + PBM 50J/cm 组在应用 PBM 后 120 和 180 分钟时痛觉阈值增加。由于发现的结果,可以认为 5-HT1A 受体参与了中枢神经系统,因为 WAY100635 能够逆转 CCI 后动物的 PBM 提供的抗伤害作用。

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