摘要:
A method of modulating cytokine mediated hepatic injury by administering compound-D SEQ ID NO:1 to a mammal. A concentration of the compound in the range of about 0.5 mg/kg to about 20 mg/kg in a physiologically acceptable formulation blocks a cytokine cascade. A therapeutic method of modulating cytokine mediated acute inflammatory, trauma induced and toxin induced hepatic injury, particularly via tumor necrosis factor modulation, is thus disclosed.
摘要翻译:通过向哺乳动物施用化合物D SEQ ID NO:1来调节细胞因子介导的肝损伤的方法。 在生理上可接受的制剂中,化合物浓度在约0.5mg / kg至约20mg / kg的范围内阻断细胞因子级联。 因此公开了调节细胞因子介导的急性炎症,创伤诱导和毒素诱导的肝损伤的治疗方法,特别是通过肿瘤坏死因子调节。
摘要:
A method of modulating cytokine mediated hepatic injury by administering deltorphins to a mammal. Deltorphin I SEQ ID NO:1, deltorphin II SEQ ID NO:2 or combinations of deltorphins I SEQ ID NO:1 and II SEQ ID NO:2 may be administered. A deltorphin concentration in the range of about 0.5 mg/kg to about 20 mg/kg in a physiologically acceptable formulation blocks a cytokine cascade in a murine model of septic shock. A therapeutic method of modulating cytokine mediated acute inflammatory, trauma induced and toxin induced hepatic injury, particularly via tumor necrosis factor modulation, is thus disclosed.
摘要翻译:通过向哺乳动物施用deltorphins来调节细胞因子介导的肝损伤的方法。 Deltorphin I SEQ ID NO:1,deltorphin II SEQ ID NO:2或deltorphins I SEQ ID NO:1和II SEQ ID NO:2的组合可以施用。 在生理上可接受的制剂中,约0.5mg / kg至约20mg / kg范围内的delphphin浓度阻断脓毒性休克鼠模型中的细胞因子级联。 因此公开了调节细胞因子介导的急性炎症,创伤诱导和毒素诱导的肝损伤的治疗方法,特别是通过肿瘤坏死因子调节。
摘要:
A method of modulating cytokine mediated hepatic injury by administering compound-D SEQ ID NO:1 to a mammal. A concentration of the compound in the range of about 0.5 mg/kg to about 20 mg/kg in a physiologically acceptable formulation blocks a cytokine cascade. A therapeutic method of modulating cytokine mediated acute inflammatory, trauma induced and toxin induced hepatic injury, particularly via tumor necrosis factor modulation, is thus disclosed.
摘要翻译:通过向哺乳动物施用化合物D SEQ ID NO:1来调节细胞因子介导的肝损伤的方法。 在生理上可接受的制剂中,化合物浓度在约0.5mg / kg至约20mg / kg的范围内阻断细胞因子级联。 因此公开了调节细胞因子介导的急性炎症,创伤诱导和毒素诱导的肝损伤的治疗方法,特别是通过肿瘤坏死因子调节。