Fosphenytoin alleviates subacute herpetic neuralgia and postherpetic neuralgia in mice

Ichiro Takasaki, Arata Inoue, Aoi Yoshida, Kimiyasu Shiraki, Y. Kitada, Saori Arai
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Abstract

This study aimed to explore the analgesic effects of fosphenytoin (fPHT) on pain-related behaviors in mouse models of subacute herpetic neuralgia (subAHN) and postherpetic neuralgia (PHN). SubAHN refers to pain experienced immediately after the disappearance of a skin rash, while PHN is characterized by persistent pain long after skin rash resolution. Our experimental approach involved the induction of acute herpes zoster-like skin lesions and pain-related responses (mechanical allodynia and hyperalgesia) in the hind paws of mice through cutaneous inoculation with herpes simplex virus type 1 (HSV-1). Subsequently, subAHN and PHN developed in the mice. Intravenous administration of fPHT (30 mg/kg) effectively mitigated HSV-1-induced subAHN and PHN. The suppressive effect of fPHT on subAHN was comparable to that of pregabalin (3 mg/kg, oral), a commonly used positive control. However, fPHT exhibited a slightly more potent effect than pregabalin in alleviating PHN. These findings suggest that intravenous fPHT could serve as a promising alternative for pain relief in both subAHN and PHN.
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Fosphenytoin减轻小鼠亚急性疱疹性神经痛和带状疱疹后神经痛
本研究旨在探讨磷妥英(fHT)对亚急性疱疹性神经痛(subAHN)和带状疱疹后神经痛(PHN)小鼠模型疼痛相关行为的镇痛作用。亚AHN指的是皮疹消失后立即出现的疼痛,而PHN的特征是皮疹消退后很长一段时间内持续疼痛。我们的实验方法涉及通过皮肤接种1型单纯疱疹病毒(HSV-1)在小鼠后爪诱导急性带状疱疹样皮肤损伤和疼痛相关反应(机械性异常疼痛和痛觉过敏)。随后,亚AHN和PHN在小鼠中发育。静脉给药fPHT(30mg/kg)有效减轻了HSV-1诱导的亚AHN和PHN。fPHT对亚AHN的抑制作用与普瑞巴林(3 mg/kg,口服)(一种常用的阳性对照)相当。然而,在减轻PHN方面,fPHT表现出比普瑞巴林略强的效果。这些发现表明,静脉注射fHT可以作为缓解亚AHN和PHN疼痛的一种有前途的替代方案。
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