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内源性D-丝氨酸在疼痛诱导的超声波发声中的功能作用。

Functional roles of endogenous D-serine in pain-induced ultrasonic vocalization.

作者信息

Tsuzuki Hitomi, Maekawa Masao, Konno Ryuichi, Hori Yuuichi

机构信息

Department of Physiology and Biological Information, Dokkyo Medical University School of Medicine, Mibu, Japan.

出版信息

Neuroreport. 2012 Nov 14;23(16):937-41. doi: 10.1097/WNR.0b013e3283595726.

Abstract

The N-methyl-D-aspartate receptor (NMDAR) is crucial for pain-related behaviors. D-Serine is synthesized from L-serine by serine racemase (SR) and modulates NMDAR functions by acting as an agonist at the glycine-binding site. We analyzed noxious stimulus-induced ultrasonic vocalization and locomotor activity in the open-field test using SR knockout (SR-KO) mice to examine the role of endogenous D-serine in mammalian behaviors. SR-KO mice emitted less ultrasonic vocalization after noxious stimulation (VAS) than wild-type (WT) mice. The locomotor activity of WT mice decreased with repeated daily exposures to the open field, whereas that of SR-KO mice remained unchanged. VAS was significantly enhanced during arthritis in WT mice, whereas it was not enhanced during arthritis in SR-KO mice. These results indicate that mice lacking the ability to produce D-serine endogenously in the brain differ from normal mice with respect to the chronic pain-induced behavioral changes.

摘要

N-甲基-D-天冬氨酸受体(NMDAR)对疼痛相关行为至关重要。D-丝氨酸由丝氨酸消旋酶(SR)从L-丝氨酸合成,并通过在甘氨酸结合位点充当激动剂来调节NMDAR功能。我们使用SR基因敲除(SR-KO)小鼠在旷场试验中分析了有害刺激诱导的超声发声和运动活动,以研究内源性D-丝氨酸在哺乳动物行为中的作用。与野生型(WT)小鼠相比,SR-KO小鼠在有害刺激(VAS)后发出的超声发声较少。WT小鼠的运动活动随着每天重复暴露于旷场而降低,而SR-KO小鼠的运动活动保持不变。WT小鼠在关节炎期间VAS显著增强,而SR-KO小鼠在关节炎期间VAS未增强。这些结果表明,大脑中缺乏内源性产生D-丝氨酸能力的小鼠在慢性疼痛诱导的行为变化方面与正常小鼠不同。

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