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A streptozotocin-induced diabetic neuropathic pain model for static or dynamic mechanical allodynia and vulvodynia: validation using topical and systemic gabapentin

机译:链脲佐菌素诱导的糖尿病性神经痛模型,用于静态或动态机械性异常性疼痛和外阴痛:使用局部和全身加巴喷丁进行验证

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摘要

Neuropathic vulvodynia is a state of vulval discomfort characterized by a burning sensation, diffuse pain, pruritus or rawness with an acute or chronic onset. Diabetes mellitus may cause this type of vulvar pain in several ways, so this study was conducted to evaluate streptozotocin-induced diabetes as a neuropathic pain model for vulvodynia in female rats. The presence of streptozotocin (50 mg/kg i.p.)-induced diabetes was initially verified by disclosure of pancreatic tissue degeneration, blood glucose elevation and body weight loss 5-29 days after a single treatment. Dynamic (shortened paw withdrawal latency to light brushing) and static (diminished von Frey filament threshold pressure) mechanical allodynia was then confirmed on the plantar foot surface. Subsequently, both static and dynamic vulvodynia was detected by application of the paradigm to the vulval region. Systemic gabapentin (75 mg/kg, i.p.) and topical gabapentin (10 % gel) were finally tested against allodynia and vulvodynia. Topical gabapentin and the control gel vehicle significantly increased paw withdrawal threshold in the case of the static allodynia model and also paw withdrawal latency in the model for dynamic allodynia when compared with the streptozotocin-pretreated group. Likewise, in the case of static and dynamic vulvodynia, there was a significant antivulvodynia effect of systemic and topical gabapentin treatment. These outcomes substantiate the value of this model not only for allodynia but also for vulvodynia, and this was corroborated by the findings not only with systemic but also with topical gabapentin.
机译:神经性外阴痛是一种外阴不适状态,其特征是灼热感,弥漫性疼痛,瘙痒或生皮,伴有急性或慢性发作。糖尿病可能以多种方式引起这种外阴痛,因此本研究旨在评估链脲佐菌素诱导的糖尿病,作为雌性大鼠外阴痛的神经性疼痛模型。链脲佐菌素(50 mg / kg i.p.)诱导的糖尿病的存在首先通过在一次治疗后5-29天揭示胰腺组织变性,血糖升高和体重减轻来证实。然后在足底足表面确认动态(缩短了到刷牙的爪缩回潜伏期)和静态(减少的冯·弗雷丝阈值压力)机械性异常性疼痛。随后,通过将范式应用于外阴区域来检测静态和动态外阴痛。最后测试了全身性加巴喷丁(75 mg / kg,腹膜内)和局部加巴喷丁(10%凝胶)的抗痛觉异常和外阴痛。与链脲佐菌素预处理组相比,在静态异常性疼痛模型的情况下,局部加巴喷丁和对照凝胶媒介物显着提高了爪退出阈值,在动态异常性疼痛模型中,爪退出潜伏期也显着增加。同样,在静态和动态外阴痛的情况下,全身和局部加巴喷丁治疗均具有显着的抗外阴痛作用。这些结果不仅证实了该模型对于异常性疼痛的价值,而且还证实了对于外阴痛的价值,这一发现不仅通过全身性研究,而且通过局部加巴喷丁研究得到证实。

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