Hormetic mechanisms

被引:322
作者
Calabrese, Edward J. [1 ]
机构
[1] Univ Massachusetts, Dept Publ Hlth, Amherst, MA 01003 USA
关键词
Biphasic; cell signaling; dose-response; hormesis; hormetic; receptor-mediated mechanism; U-shaped; GONADOTROPIN-RELEASING-HORMONE; ALPHA-LACTALBUMIN PRODUCTION; ACTIVATED PROTEIN-KINASE; NEURAL PROGENITOR CELLS; SHAPED DOSE RESPONSES; GROWTH-FACTOR; NITRIC-OXIDE; BIPHASIC REGULATION; DNA-SYNTHESIS; IN-VIVO;
D O I
10.3109/10408444.2013.808172
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
This article provides the first extensive documentation of mechanisms of hormetic dose/concentration responses. The mechanisms selected were principally those mediated via receptor and/or cell signaling pathways. Mechanisms are reported for greater than 100 agents affecting nearly 400 dose/concentration responses from a wide range of chemical classes, affecting a broad range of cell types and endpoints. Regardless of the model (i.e. in vitro or in vivo), inducing agent, endpoint, or receptor/cell signaling pathway mediated mechanism, the quantitative features of the hormetic dose/concentration responses are similar, suggesting that the magnitude of the response is a measure of biological plasticity, within a broad range of biological contexts. These findings represent an important advance in the understanding of the hormetic dose/concentration response, its generalizability and potential biomedical applications, including drug discovery/efficacy assessment and the risk assessment process.
引用
收藏
页码:580 / 606
页数:27
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