Acetaminophen reduces lipopolysaccharide-induced fever by inhibiting cyclooxygenase-2

详细信息    查看全文

• 作者：Linda Engstr&ouml ; m Ruud^a ; Daniel Bj&ouml ; rk Wilhelms^a ; Anna Eskilsson^a ; Ana Maria Vasilache^a ; ^b ; Louise Elander^a ; David Engblom^a ; ¹ ; Anders Blomqvist^a ; ¹ ; ^{anders.blomqvist@liu.se}
• 关键词：Fever ; Cyclooxygenase-2 ; Cyclooxygenase-1 ; Microsomal prostaglandin E synthase-1 ; Gene dosage ; Hypothalamus
• 刊名：Neuropharmacology
• 出版年：2013
• 出版时间：August, 2013
• 年：2013
• 卷：71
• 期：Complete
• 页码：124-129
• 全文大小：925 K

文摘

Acetaminophen is one of the world's most commonly used drugs to treat fever and pain, yet its mechanism of action has remained unclear. Here we tested the hypothesis that acetaminophen blocks fever through inhibition of cyclooxygenase-2 (Cox-2), by monitoring lipopolysaccharide induced fever in mice with genetic manipulations of enzymes in the prostaglandin cascade. We exploited the fact that lowered levels of a specific enzyme make the system more sensitive to any further inhibition of the same enzyme. Mice were immune challenged by an intraperitoneal injection of bacterial wall lipopolysaccharide and their body temperature recorded by telemetry. We found that mice heterozygous for Cox-2, but not for microsomal prostaglandin E synthase-1 (mPGES-1), displayed attenuated fever, indicating a rate limiting role of Cox-2. We then titrated a dose of acetaminophen that did not inhibit the lipopolysaccharide-induced fever in wild-type mice. However, when the same dose of acetaminophen was given to Cox-2 heterozygous mice, the febrile response to lipopolysaccharide was strongly attenuated, resulting in an almost normalized temperature curve, whereas no difference was seen between wild-type and heterozygous mPGES-1 mice. Furthermore, the fever to intracerebrally injected prostaglandin E₂ was unaffected by acetaminophen treatment. These findings reveal that acetaminophen, similar to aspirin and other non-steroidal anti-inflammatory drugs, is antipyretic by inhibiting cyclooxygenase-2, and not by inhibiting mPGES-1 or signaling cascades downstream of prostaglandin E₂.