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2型糖尿病小鼠模型(TSOD小鼠)糖尿病前期状态下的周围神经病变涉及背根神经节中TRPV1的表达。

Peripheral neuropathy in the pre-diabetic state of the type 2 diabetes mouse model (TSOD mice) involves TRPV1 expression in dorsal root ganglions.

作者信息

Shida Kyoko, Ohsawa Masahiro, Takahashi Satoru, Ota Haruko, Tamura Tetsuya, Kusama Nobuyoshi, Nakasone Mina, Yamazaki Hisaaki, Sobue Kazuya

机构信息

Department of Anesthesiology and Intensive Care Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Laboratory of CNS Pharmacology, Nagoya City University Graduate School of Pharmaceutical Sciences, Nagoya, Japan.

出版信息

IBRO Neurosci Rep. 2022 Feb 8;12:163-169. doi: 10.1016/j.ibneur.2022.02.001. eCollection 2022 Jun.

Abstract

Peripheral neuropathy, which is a complication of diabetes mellitus (DM), is thought to occur in the pre-DM state, being known as impaired glucose tolerance (IGT) neuropathy, although its pathogenesis is unknown. Since it is reversible, an effective treatment at the pre-DM stage could stop the progression of peripheral neuropathy and improve patients' quality of life and reduce medical costs. We investigated the hypersensitivity to mechanical and thermal stimuli during the pre-DM state in Tsumura Suzuki Obese Diabetes (TSOD) mice, a type 2 DM mouse model. The expression pattern of the Transient Receptor Potential Vanilloid 1 (TRPV1)-positive cells in the dorsal root ganglia (DRG) was examined in TSOD mice, which showed a pre-DM state at 5-12 weeks of age and decreased mechanical and thermal nociceptive thresholds. Additionally, the size of TRPV1-positive cells in TSOD mice increased compared with that in non-diabetic controls (Tsumura Suzuki Non-Obesity; TSNO). Furthermore, the expression of TRPV1 on myelinated nerve fibers (neurofilament heavy-positive cells) had significantly increased. Thus, TSOD mice in the pre-DM state at 5-12 weeks of age could be a useful animal model of IGT neuropathy. We also hypothesized that the development of IGT neuropathy may involve a switch in TRPV1 expression from small, unmyelinated neurons to large, myelinated neurons in the DRG.

摘要

周围神经病变是糖尿病(DM)的一种并发症,尽管其发病机制尚不清楚,但人们认为它在糖尿病前期状态即糖耐量受损(IGT)神经病变时就已发生。由于它是可逆的,在糖尿病前期阶段进行有效治疗可以阻止周围神经病变的进展,提高患者生活质量并降低医疗成本。我们在2型糖尿病小鼠模型津村铃木肥胖糖尿病(TSOD)小鼠的糖尿病前期状态下,研究了其对机械和热刺激的超敏反应。在5至12周龄呈现糖尿病前期状态且机械和热痛觉阈值降低的TSOD小鼠中,检测了背根神经节(DRG)中瞬时受体电位香草酸受体1(TRPV1)阳性细胞的表达模式。此外,与非糖尿病对照(津村铃木非肥胖;TSNO)相比,TSOD小鼠中TRPV1阳性细胞的大小增加。而且,有髓神经纤维(神经丝重链阳性细胞)上TRPV1的表达显著增加。因此,5至12周龄处于糖尿病前期状态的TSOD小鼠可能是IGT神经病变的有用动物模型。我们还推测,IGT神经病变的发生可能涉及DRG中TRPV1表达从小的无髓神经元向大的有髓神经元的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3237/8850332/febb85b64796/gr1.jpg

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