Homocysteine, ER Stress and Alcoholic Liver Injury.

描述（由申请人提供）：我们已经证明，胃内酒精喂养的小鼠会出现高同型半胱氨酸血症、ER应激和脂肪性肝炎。喂食甜菜碱可以防止酒精的所有这些影响。基于我们以前的研究，我们已经开发了五个具体的目标，测试的假设，即同型半胱氨酸诱导的内质网应激在酒精性肝病的发病机制中起着关键作用：目的1。确定肝脏特异性缺失Grp 78对酒精或高甲硫氨酸低叶酸（HMLF）喂养引起的肝损伤的易感性的影响：这项工作包括繁殖和表型条件敲除小鼠，以及Grp 78缺失影响的体外和体内研究;目的2.确定分子伴侣在抑制酒精和同型半胱氨酸诱导的ER应激和脂肪性肝炎中的有效性：这项工作包括作为原理证明的体外研究和保护作用的体内研究。目标3：检查JNK在内质网应激诱导的肝损伤中的作用：这些研究将评估JNK 1、2或两者的反义核酸在体外原理验证研究和酒精和HMLF模型中的体内研究中的作用。前三个目的是检验这一假设，即ER应激是胃内小鼠模型中酒精性肝病严重程度的主要决定因素。目标4。通过检验酒精性脂肪肝是由ER应激诱导的Insig-1失调导致SREBP激活引起的假设，确定ER应激在肝脏脂质蓄积中的机制和作用。目标5。通过检验以下假设确定BHMT在酒精诱导的肝损伤中的作用：BHMT的反应是高同型半胱氨酸血症发展和随后ER应激下游激活导致脂肪变性和损伤的关键因素;这项工作将包括物种差异的研究（小鼠与大鼠）在BHMT转录调节中的作用，NF-κ B在BHMT抑制中的作用，同型半胱氨酸和甜菜碱诱导BHMT的机制，以及通过在大鼠模型中用酒精喂养CBHcy来抑制BHMT的效果，以测试是否可以克服对酒精性肝病的抵抗。这项工作将导致预防或治疗酒精性肝病的新方法，并将扩大我们对肝脏ER应激的原因和影响的了解。

DESCRIPTION (provided by applicant): We have demonstrated that the intragastric alcohol fed mouse develops hyperhomocysteinemia, ER stress and steatohepatitis. Feeding betaine prevents all of these effects of alcohol. Based upon our previous studies we have developed five specific aims which test the hypothesis that ER stress induced by homocysteine plays a key role in the pathogenesis of alcoholic liver disease: Aim 1. Determine the effect of liver specific deletion of Grp78 on the susceptibility to liver injury from alcohol or high methionine low folate (HMLF) feeding: this work includes breeding and phenotyping conditional knockout mice, and in vitro and in vivo studies of the effect of deletion of Grp78; Aim 2. Determine the effectiveness of molecular chaperones in inhibiting alcohol and homocysteine-induced ER stress and steatohepatitis: this work includes in vitro studies as proof of principle and in vivo studies of the protective effect. Aim 3. Examine the contribution of JNK in ER stress-induced liver injury: these studies will assess the effects of antisense to JNK1, 2, or both in vitro in proof of principle studies and in vivo studies in the alcohol and HMLF models. The first three aims test the hypothesis that ER stress is a major determinant of the severity of alcohol liver disease in the intragastric mouse model. Aim 4. Determine the mechanism and role of ER stress in hepatic lipid accumulation by testing the hypothesis that alcoholic fatty liver is caused by ER stress induced dysregulation of Insig-1 leading to SREBP activation. Aim 5. Determine the role of BHMT in alcohol-induced liver injury by testing the hypothesis that the response of BHMT is a critical factor in the development of hyperhomocysteinemia and subsequent downstream activation of ER stress resulting in steatosis and injury; this work will include studies of the species differences (mouse versus rat) in the transcriptional regulation of BHMT, the role of NF-kB in repression of BHMT, the mechanism of induction of BHMT by homocysteine and betaine, and the effect of inhibiting BHMT by feeding CBHcy with alcohol in the rat model to test if the resistance to alcoholic liver disease can be overcome. This work will lead to new approaches to prevent or treat alcoholic liver disease and will expand our knowledge of the causes and effects of ER stress in the liver.