Bhagwandeen B S, Apte M, Manwarring L, Dickeson J
J Pathol. 1987 May;152(1):47-53. doi: 10.1002/path.1711520107.
The role of endotoxin in the pathogenesis of progressive liver disease is receiving increasing attention, but remains controversial. Similarly, although alcoholic hepatitis is now recognized as the transitional link between alcoholic fatty liver and advanced alcoholic liver disease, the aetiology of liver cell necrosis in alcoholic hepatitis is not known. Rats fed a nutritionally adequate liquid alcohol diet according to the formula of Lieber and DeCarli developed fatty livers. Littermates fed an identical diet and challenged with small IV doses (1 microgram/g body weight) of E. coli lipopolysaccharide endotoxin (LPS) developed focal necrotizing hepatitis. Control littermates fed an identical calorie balanced but alcohol free diet and challenged with identical doses of LPS did not develop any liver lesions. The hepatocyte necrosis with associated inflammatory changes induced by LPS in fatty livers has some features of early human alcoholic hepatitis and suggests that progressive alcohol induced damage may be multifactorial in origin.
内毒素在进行性肝病发病机制中的作用日益受到关注,但仍存在争议。同样,尽管酒精性肝炎目前被认为是酒精性脂肪肝和晚期酒精性肝病之间的过渡环节,但酒精性肝炎中肝细胞坏死的病因尚不清楚。按照Lieber和DeCarli的配方给予营养充足的液体酒精饮食的大鼠会发展为脂肪肝。给予相同饮食并静脉注射小剂量(1微克/克体重)大肠杆菌脂多糖内毒素(LPS)的同窝幼崽会发展为局灶性坏死性肝炎。给予相同热量平衡但不含酒精饮食并注射相同剂量LPS的对照同窝幼崽未出现任何肝脏病变。LPS在脂肪肝中诱导的伴有炎症变化的肝细胞坏死具有早期人类酒精性肝炎的一些特征,这表明酒精诱导的进行性损伤可能是多因素起源的。