Filkins J P, Buchanan B J
Circ Shock. 1977;4(3):253-8.
ATP-Mg++ (10 mumoles/100 g, iv) increased the LD50 for Salmonella enteritidis lipopolysaccharide (endotoxin) in male Holtzman rats (300 +/- 10 g) from 1.3 to 6.0 mg/rat. While endotoxin at 3 mg/rat iv 5 hr previously induced hypoglycemia to 12 +/- 4 mg/dl, ATP cotreatment blunted the hypoglycemia; i.e., plasma glucose values were 78 +/- 6 mg/dl. ATP treatment prevented the depression in gluconeogenesis induced by endotoxin as evaluated in vivo by the conversion of 14C-alanine to 14C-glucose. ATP treatment also reduced the hypercatabolism of U-14 C-glucose to 14CO2 in vivo and by epididymal fat pads in vitro. A role for ATP in preventing disruption of glucose homeostasis and development of endotoxin shock via counteracting insulin is suggested.
ATP - Mg++(10微摩尔/100克,静脉注射)使雄性霍尔兹曼大鼠(300±10克)对肠炎沙门氏菌脂多糖(内毒素)的半数致死量从1.3毫克/只提高到6.0毫克/只。虽然之前5小时静脉注射3毫克/只内毒素会使血糖降至12±4毫克/分升,但ATP联合治疗可减轻低血糖;即血浆葡萄糖值为78±6毫克/分升。通过14C - 丙氨酸向14C - 葡萄糖的转化在体内评估发现,ATP治疗可防止内毒素诱导的糖异生抑制。ATP治疗还减少了体内以及附睾脂肪垫体外U - 14C - 葡萄糖向14CO2的高分解代谢。提示ATP通过对抗胰岛素在预防葡萄糖稳态破坏和内毒素休克发展中发挥作用。