HSP-Dependent Protection Against Gastrointestinal Diseases

Author(s): Tohru Mizushima

Journal Name: Current Pharmaceutical Design

Volume 16 , Issue 10 , 2010

Become EABM
Become Reviewer
Call for Editor


It is well known that heat shock proteins (HSPs) are induced by various stressors in order to confer protection against such stressors. Since stressor-induced tissue damage is involved in various diseases, especially gastrointestinal diseases, such as gastric ulcer, it has been thought that HSPs are protective against these diseases. Indirect lines of evidence, such as identification of geranylgeranylacetone (GGA, a leading anti-ulcer drug in Japanese market) as non-toxic HSP-inducer, suggest that HSPs provide a major protective mechanism against irritant-induced gastric lesions. However, no direct evidences that support this notion exits. Furthermore, because GGA has other gastroprotective effects, it was not clear whether HSP-induction by GGA is the main mechanism for its anti-ulcer effect. In this article, I review our recent work on protective roles of HSPs against gastrointestinal diseases, using transgenic mice. We obtained genetic evidence showing not only that HSPs are protective against irritant-induced gastric lesions but also that GGA achieves its anti-ulcer effect through induction of HSPs. We also obtained genetic evidence that HSPs are protective against inflammatory bowel disease (IBD)-related colitis and lesions of small intestine. Furthermore, we found that GGA is effective against these diseases. Based on these observations, we propose that non-toxic HSP-inducers, such as GGA are therapeutically beneficial for these diseases.

Keywords: HSP70, HSF1, gastric ulcer, IBD, lesions of the small intestine, GGA

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2010
Page: [1190 - 1196]
Pages: 7
DOI: 10.2174/138161210790945986
Price: $65

Article Metrics

PDF: 5