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预处理是激效的一部分 I:文献记录、剂量反应特征和机制基础。

Preconditioning is hormesis part I: Documentation, dose-response features and mechanistic foundations.

机构信息

Department of Environmental Health Sciences, Morrill I, N344, University of Massachusetts, Amherst MA 01003, United States.

出版信息

Pharmacol Res. 2016 Aug;110:242-264. doi: 10.1016/j.phrs.2015.12.021. Epub 2016 Jan 3.

Abstract

This article provides the first extensive documentation of the dose response features of pre- and postconditioning. Pre- and postconditioning studies with rigorous study designs, using multiple doses/concentrations along with refined dose/concentration spacing strategies, often display hormetic dose/concentration response relationships with considerable generality across biological model, inducing (i.e., conditioning) agent, challenging dose treatment, endpoint, and mechanism. Pre- and postconditioning hormesis dose/concentration-response relationships are reported for 154 diverse conditioning agents, affecting more than 550 dose/concentration responses, across a broad range of biological models and endpoints. The quantitative features of the pre- and postconditioning-induced protective responses are modest, typically being 30-60% greater than control values at maximum, findings that are consistent with a large body (>10,000) of hormetic dose/concentration responses not related to pre- and postconditioning. Regardless of the biological model, inducing agent, endpoint or mechanism, the quantitative features of hormetic dose/concentration responses are similar, suggesting that the magnitude of response is a measure of biological plasticity. This paper also provides the first documentation that hormetic effects account for preconditioning induced early (1-3h) and delayed (12-72h) windows of protection. These findings indicate that pre- and postconditioning are specific types of hormesis.

摘要

本文首次全面记录了预处理和后处理的剂量反应特征。采用严格的研究设计、使用多种剂量/浓度以及精细的剂量/浓度间隔策略进行的预处理和后处理研究,通常显示出具有相当普遍性的激素剂量/浓度反应关系,涉及多种生物学模型、诱导(即调节)剂、挑战性剂量处理、终点和机制。本文报道了 154 种不同的调节剂的预处理和后处理的激素剂量/浓度反应关系,涉及 550 多个剂量/浓度反应,涵盖了广泛的生物学模型和终点。预处理和后处理诱导的保护反应的定量特征适中,通常在最大值时比对照值高 30-60%,这些发现与大量 (>10,000) 与预处理和后处理无关的激素剂量/浓度反应一致。无论生物学模型、诱导剂、终点或机制如何,激素剂量/浓度反应的定量特征都相似,这表明反应的幅度是生物可塑性的衡量标准。本文还首次证明了激素作用解释了预处理诱导的早期(1-3 小时)和延迟(12-72 小时)保护窗口。这些发现表明预处理和后处理是特定类型的激素作用。

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