Abstract
Activation of the unfolded protein response (UPR) has been suggested to attenuate renal ischemia-reperfusion (I/R) injury. We recently found a compound, namely BIX, that activated the UPR selectively through the activating transcription factor 6 pathway. This study examined the effect of BIX on renal I/R injury in mice. BIX selectively up-regulated renal BiP mRNA and protein. Pretreatment with BIX significantly ameliorated renal I/R injury. Co- administration of BIX and tunicamycin, a non-selective UPR inducer, provided no additional protection. Our results suggest that the UPR activation by BIX leads to a novel drug therapy against renal I/R injury. © 2009 The Japanese Pharmacological Society.
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Prachasilchai, W., Sonoda, H., Yokota-Ikeda, N., Ito, K., Kudo, T., Imaizumi, K., & Ikeda, M. (2009). The protective effect of a newly developed molecular chaperone- inducer against mouse ischemic acute kidney injury. Journal of Pharmacological Sciences, 109(2), 311–314. https://doi.org/10.1254/jphs.08272SC
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