Jang Yujin, Lee Min Hee, Park Jong-Hwan, Han Seung-Yun, Kim Dong Kwan
Departments of aPhysiology bAnatomy cMyunggok Medical Research Institute, Konyang University College of Medicine, Daejeon dLaboratory Animal Medicine, College of Veterinary Medicine, Chonnam National University, Gwangju, Republic of Korea.
Neuroreport. 2016 Mar 23;27(5):356-60. doi: 10.1097/WNR.0000000000000549.
Toll-like receptors (TLRs) are innate immunity-related receptors. Many studies have indicated the involvement of TLRs in neurophysiology and neuropathology. One study showed that TLR3 regulates hippocampal memory and is highly expressed in the mesolimbic dopamine system, suggesting that TLR3 signaling may regulate alcohol consumption. The present study assessed the potential role of TLR3 in alcohol intake pattern. We used adult BalbC wild-type mice and TLR3 knockout mice and tested two-bottle alcohol preference over 15 days and one-bottle 2 or 4 h drinking in the dark over 4 consecutive days. The 10% alcohol consumption rate of TLR3 knockout mice increased on the 24 h free-choice test. Our findings support a potential regulatory role of TLR3 in alcohol consumption.
Toll样受体(TLRs)是与先天免疫相关的受体。许多研究表明TLRs参与神经生理学和神经病理学过程。一项研究显示,TLR3调节海马体记忆,并且在中脑边缘多巴胺系统中高度表达,这表明TLR3信号传导可能调节酒精摄入。本研究评估了TLR3在酒精摄入模式中的潜在作用。我们使用成年BalbC野生型小鼠和TLR3基因敲除小鼠,进行了为期15天的两瓶酒精偏好测试,以及连续4天在黑暗中进行的一瓶2或4小时饮酒测试。在24小时自由选择测试中,TLR3基因敲除小鼠的10%酒精消耗率有所增加。我们的研究结果支持TLR3在酒精消耗中具有潜在调节作用。