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首页> 外文期刊>Diabetes/metabolism research and reviews >C-fos expression at the spinal dorsal horn of streptozotocin-induced diabetic rats.
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C-fos expression at the spinal dorsal horn of streptozotocin-induced diabetic rats.

机译:C-fos在链脲佐菌素诱导的糖尿病大鼠的脊髓背角表达。

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摘要

BACKGROUND: Pain during diabetic neuropathy is associated with peripheral nerve damage but recent evidences suggest the occurrence of central effects. We used the activation of the c-fos protooncogene to study the activity of spinal dorsal horn neurons in streptozotocin (STZ)-induced diabetic rats in the absence of stimulation or in response to innocuous or noxious stimuli. METHODS: Four weeks after saline or STZ (50 mg/kg) injection, rats were anaesthetized and either not further manipulated or submitted to innocuous (gentle touch), noxious mechanical (pinching) or noxious thermal (radiant heat) stimulation of the hindlimb skin. In each experimental situation, the numbers of Fos-immunoreactive (Fos-IR) neurons occurring in the superficial (laminae I-II) or deep (laminae III-V) dorsal horn were compared. RESULTS: In the absence of stimulation, STZ-injected rats presented significantly higher numbers of Fos-IR neurons than controls, both in the superficial and deep dorsal horn (DDH). In comparison with the respective baseline levels, innocuous stimulation did not induce a significant increase in the numbers of Fos-IR neurons in controls or STZ-rats. Noxious mechanical and noxious thermal stimuli increased the numbers of Fos-IR neurons, both in control and STZ-rats, but in a more pronounced manner when diabetic rats were subjected to noxious mechanical stimulation. CONCLUSIONS: The present study demonstrates that the responses of spinal cord neurons are strongly affected during diabetes. The higher baseline neuronal activity probably underlies the spontaneous pain detected during diabetes since the spinal dorsal horn is the major relay station in the ascending transmission of nociceptive input to the brain.
机译:背景:糖尿病性神经病患者的疼痛与周围神经损伤有关,但最近的证据表明发生了中枢效应。我们使用c-fos原癌基因的激活来研究在无刺激或无害或有害刺激下链脲佐菌素(STZ)诱导的糖尿病大鼠中脊髓背角神经元的活性。方法:注射生理盐水或STZ(50 mg / kg)后四周,麻醉大鼠,不对其进行进一步处理,也不对后肢皮肤进行无害(温和触摸),有毒机械(捏)或有毒热(辐射热)刺激。 。在每种实验情况下,都比较了浅(背板I-II)或深背板(III-V)背角中Fos免疫反应(Fos-IR)神经元的数量。结果:在没有刺激的情况下,注射STZ的大鼠在浅背角和深背角(DDH)中的Fos-IR神经元数量明显高于对照组。与各自的基线水平相比,无害刺激在对照组或STZ大鼠中并未引起Fos-IR神经元数量的显着增加。有毒的机械刺激和有毒的热刺激均增加了对照组和STZ大鼠的Fos-IR神经元数量,但当糖尿病大鼠受到有毒的机械刺激时,这种作用更为明显。结论:本研究表明糖尿病期间脊髓神经元的反应受到强烈影响。较高的基线神经元活动可能是糖尿病期间检测到的自发性疼痛的基础,因为脊髓背角是伤害性输入向大脑上升传递的主要中继站。

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