Abstract:This report discusses a unique drug-induced hepatotoxicity in cynomolgus monkeys treated orally with a novel potassium sparing experimental diuretic, [2,6-bis(4-chlorophenyl
“…In humans, granulomatous response in liver has been associated with several drugs (14). Microgranulomas were described in monkeys treated with an experimental diuretic (16), in dogs treated with a protease inhibitor (17), and in rats given a sterol compound (13). The microgranulomas in livers of dogs in this study consisted mainly of mononuclear phagocytes, many of which were pigmented, a result of incomplete degradation of senescent, lipofuscin-filled hepatocytes.…”
Section: Discussionmentioning
confidence: 99%
“…In humans, granulomatous response in liver has been associated with several drugs (14). Microgranulomas were described in monkeys treated with an experimental diuretic (16), in dogs treated with a protease inhibitor (17), and in rats given a sterol compound (13). The (27) and was present at all sacrifice time points in this study, but severity was less at 104 wk than at 52 wk.…”
The chronic toxicity of atorvastatin (AT), an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, was evaluated in beagle dogs. Dogs were treated with 0, 10, 40, or 120 mg/kg of AT daily. Treatment
“…In humans, granulomatous response in liver has been associated with several drugs (14). Microgranulomas were described in monkeys treated with an experimental diuretic (16), in dogs treated with a protease inhibitor (17), and in rats given a sterol compound (13). The microgranulomas in livers of dogs in this study consisted mainly of mononuclear phagocytes, many of which were pigmented, a result of incomplete degradation of senescent, lipofuscin-filled hepatocytes.…”
Section: Discussionmentioning
confidence: 99%
“…In humans, granulomatous response in liver has been associated with several drugs (14). Microgranulomas were described in monkeys treated with an experimental diuretic (16), in dogs treated with a protease inhibitor (17), and in rats given a sterol compound (13). The (27) and was present at all sacrifice time points in this study, but severity was less at 104 wk than at 52 wk.…”
The chronic toxicity of atorvastatin (AT), an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, was evaluated in beagle dogs. Dogs were treated with 0, 10, 40, or 120 mg/kg of AT daily. Treatment
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