Tsuzuki Hitomi, Maekawa Masao, Konno Ryuichi, Hori Yuuichi
Department of Physiology and Biological Information, Dokkyo Medical University School of Medicine, Mibu, Japan.
Neuroreport. 2012 Nov 14;23(16):937-41. doi: 10.1097/WNR.0b013e3283595726.
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.
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。