期刊
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
卷 43, 期 10, 页码 1039-1051出版社
WILEY
DOI: 10.1111/eci.12141
关键词
5HT(3) receptor; beta-amyloid; calcineurin; neuroinflammation; tropisetron
BackgroundAlzheimer's disease (AD) is a neurodegenerative disorder featured by deposition of beta-amyloid (A) plaques in the hippocampus and associated cortices and progressive cognitive decline. Tropisetron, a selective 5-HT3 receptor antagonist, is conventionally used to counteract chemotherapy-induced emesis. Recent investigations describe antiphlogistic properties for tropisetron. It has been shown that tropisetron protects against rat embolic stroke. We investigated protective properties of tropisetron in a beta-amyloid (A) rat model of AD and possible involvement of 5-HT3 receptors. Material and methodsA (1-42) was injected into the hippocampus of male rats. Animals were treated intracerebroventricularly with tropisetron, mCPBG (selective 5-HT3 receptor agonist) or mCPBG plus tropisetron on days 1, 3, 5 and 7. Seven days following A administration, inflammatory markers (TNF-, COX-2, iNOS and NF-B), apoptotic markers (caspase 3 cytochrome c release) and calcineurin phosphatase activity were assessed in hippocampus. ResultsSeven days following A inoculation, control animals displayed dramatic increase in TNF-, COX-2, iNOS, NF-B, active caspase 3, cytochrome c release and calcineurin phosphatase activity in the hippocampus. Tropisetron significantly diminished the elevated levels of these markers and reversed the cognitive deficit. Interestingly, tropisetron was also found to be a potent inhibitor of calcineurin phosphatase activity. The selective 5-HT3 receptor agonist mCPBG, when co-administered with tropisetron, completely reversed the procognitive and anti-apoptotic properties of tropisetron while it could only partially counteract the anti-inflammatory effects. mCPBG alone significantly aggravated A-induced injury. ConclusionOur findings indicate that tropisetron protects against A-induced neurotoxicity in vivo through both 5-HT3 receptor-dependent and independent pathways.
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