Localization of heat shock proteins and histopathological changes in the kidneys of transported pigs

Livestock Science

Volumn 118, Issue 3, 2008, Pages 231-237

  Bao, Endong ^a   Sultan, K R ^b   Nowak, B ^c   Hartung, J ^c  

^a NANJING AGRICULTURAL UNIVERSITY   (China)

^b UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^c UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

Author keywords

Heat shock protein; Kidney; Pigs; Stress; Transportation

Indexed keywords

SUIDAE;

EID: 54349119854     PISSN: 18711413     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.livsci.2008.01.028     Document Type: Article

References (38)

1. Beck F.X., Neuhofer W., and Muller E. Molecular chaperones in the kidney: distribution, putative roles, and regulation. Am. J. Physiol. Renal. 279 (2000) F203-F215
2. Beck F.X., Grunbein R., Lugmayr K., and Neuhofer W. Heat shock proteins and the cellular response to osmotic stress. Cell. Physiol. Biochem. 10 (2000) 303-306
3. Chatterjee P.K., Cuzzocrea S., Brown P.A., Zacharowski K., Stewart K.N., Mota-Filipe H., and Thiemermann C. Tempol, a membrane-permeable radical scavenger, reduces oxidant stress-mediated renal dysfunction and injury in the rat. Kidney Int. 58 (2000) 658-673
4. Currie R.W., Tanguay R.M., and Kingma J.G. Heat-shock response and limitation of tissue necrosis during occlusion/reperfusion in rabbit hearts. Circulation 87 (1993) 963-971
5. Deshaies R.J., Koch B.D., Werner-Washburne M., Craig E.A., and Schekman R. A subfamily of stress proteins facilitates translocation of secretory and mitochondrial precursor polypeptides. Nature 332 (1988) 800-805
6. Gauthaman K., Banerjee S.K., Dinda A.K., Ghosh C.C., and Maulik S.K. Terminalia arjuna (Roxb.) protects rabbit heart against ischemic-reperfusion injury: role of antioxidant enzymes and heat shock protein. J. Ethnopharmacol. 96 (2005) 403-409
7. Gradin M., McGuire J., Wenger R.H., Kvietikova L., Whitelaw M.L., Toftgard R., Tora L., Gassmann M., and Poellinger L.A. Function interference between hypoxia and dioxin signal transduction pathways: competition for recruitment of the Arnt transcription factor. Mol. Cell. Biol. 16 (1996) 5221-5231
8. Highttower L.E. Heat shock, stress protein, chaperones, and proteotoxicity. Cell 66 (1991) 191-197
9. Huot J., Houle F., Spitz D.R., and Landry J. HSP27 phosphorylation-mediated resistance against actin fragmentation and cell death induced by oxidative stress. Cancer Res. 56 (1996) 273-279
10. Kelly K.J. Heat shock (stress response) proteins and renal ischemia/reperfusion injury. Contrib. Nephrol. 148 (2005) 86-106
11. 70 response. Can. J. Appl. Physiol. 23 (1998) 245-260
12. Klemcke H.G. Responses of the porcine pituitary-adrenal axis to chronic intermittent stressor. Domest. Anim. Endocrinol. 11 (1994) 133-149
13. Kim J., Kil I.S., Seok Y.M., Yang E.S., Kim D.K., Lim D.G., Park J.W., Bonventre J.V., and Park K.M. Orchiectomy attenuates post-ischemic oxidative stress and ischemia/reperfusion injury in mice. A role for manganese superoxide dismutase. J. Biol. Chem. 281 (2006) 20349-20359
14. LaemmLi U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685
15. Lee W.C., Lin K.Y., Chiu Y.T., Lin J.H., Cheng H.C., Huang H.C., Yang P.C., Liu S.K., and Mao S.J. Substantial decrease of heat shock protein 90 in ventricular tissues of two sudden-death pigs with hypertrophic cardiomyopathy. FASEB J. 10 (1996) 1198-1204
16. Li Y.-b., Bao E.-d., Wang Z.-l., and Zhao R.-q. Detection of HSP mRNA transcription in transport stressed pigs by fluorescence quantitative RT-PCR. Sci. Agri. Sini. 6 (2007) 361-367
17. Marber M.S., Mestril R., Chi S.H., Sayern M.R., Yellon D.M., and Dillmann W.H. Overexpression of the rat inducible 70-KD heat stress protein in a transgenic mouse increases the resistance of the heart to ischemia injury. J. Clini. Invest. 95 (1995) 1446-1456
18. Marruchella G., Di Leonardo M., Di Guardo G., Romanucci M., Marà M., Tiscar P.G., Mosca F., and Della Salda L. Heat shock proteins (HSPs) 27, 72 and 73 in normal and pre-ulcerative mucosa of the gastric pars oesophagea in swine. J.Comp.Pathol. 131 (2004) 10-17
19. McLemore E.C., Tessier D.J., Komalavilas P., Thresher J., and Brophy C.M. The yin and yang of vascular smooth muscle tone. J. Am. Coll. Surg. 199 (2004) 106-107
20. McLemore E.C., Tessier D.J., Thresher J., Komalavilas P., and Brophy C.M. Role of the small heat shock proteins in regulating vascular smooth muscle tone. J. Am. Coll. Surg. 201 (2005) 30-36
21. Michaud S., Marin R., and Tanguay R.M. Regulation of heat shock gene induction and expression during Drosophila development. Cell. Mol. Life Sci. 53 (1997) 104-113
22. Natelson B.H., Ottenweller J.E., Cook J.A., Pitman D., McCarty R., and Tapp W.N. Effect of stressor intensity on habituation of the adrenocortical stress response. Physiol. Behav. 43 (1988) 41-46
23. Park K.M., Chen A., and Bonventre J.V. Prevention of kidney ischemia/reperfusion-induced functional injury and JNK, p38, and MAPK kinase activation by remote ischemic pretreatment. J. Biol. Chem. 276 (2001) 11870-11876
24. Park K.M., Kramers C., Vayssier-Taussat M., Chen A., and Bonventre J.V. Prevention of kidney ischemia/reperfusion-induced functional injury, MAPK and MAPK kinase activation, and inflammation by remote transient ureteral obstruction. J. Biol. Chem. 277 (2002) 2040-2049
25. Pelham H.R.B. Speculations of the functions of the major heat shock and glucose regulated proteins. Cell 46 (1986) 959-961
26. Plumier C., Krueger A.M., Currie R.W., Kontoyiannis D., Kollias G., and Pagoulatos G.N. Transgenic mice expressing the human inducible Hsp70 have hippocampal neurons resistant to ischemic injury. Cell Stress Chaperon. 2 (1997) 162-167
27. Schütte A. Transporttauglichkeit von Schweinen. In: Hartung J. (Ed). Hygiene und Tierschutz beim Tiertransport. Proc. Deutsche Veterinärmedizinische Gesellschaft, Hannover 8.-9., S (1994) 83-98
28. Seok Y.M., Kim J.N., Choi K.C., Yoon C.H., Boo Y.C., Park Y.K., and Park K.M. Wen-pi-tang-Hab-Wu-ling-san attenuates kidney ischemia/reperfusion injury in mice: a role for antioxidant enzymes and heat-shock proteins. J. Ethnopharmacol. 112 (2007) 333-340
29. Sepponen K., and Pösö A.R. The inducible form of heat shock protein 70 in the serum, colon and small intestine of the pig: comparison to conventional stress markers. Vet. J. 171 (2006) 519-524
30. Snoeckx L.H., Cornelussen R.N., Van Nieuwenhoven F.A., Reneman R.S., and Van Der Vusse G.J. Heat shock proteins and cardiovascular pathophysiology. Physiol. Rev. 81 (2001) 1461-1497
31. Thadhani R., Pascual M., and Bonventre J.V. Acute renal failure. New Engl. J. Med. 334 (1996) 1448-1460
32. Viswanathan M., Rivera O., and Short B.L. Heat-shock protein 90 involved in pulsatile flow induced dilatation of the rat middle cerebral artery. J Vasc Res. 36 (1999) 524-527
33. Walker D.M., Pasini E., Kucukoglu S., Marber M.S., Iliodromitis E., Ferrari R., and Yellon D.M. Heat stress limits infarct size in isolated perfused rabbit heart. Cardiovasc. Res. 27 (1993) 962-967
34. Wang D., Mcmillin J.B., Bick R., and Buja L.M. Response of the neonatal rat cardiomyocyte in culture to energy depletion: effects of cytokines, nitric oxide, and heat shock proteins. Lab. Invest. 75 (1996) 809-818
35. Witek B., Koataj A., and Krol T. Adaptive changes of activity of lysosomal enzymes in the liver, kidneys and spleen of pigs subjected to transport stress. Archiv fur Tierzucht. 39 (1996) 55-59
36. Wu T., and Tanguay R.M. Antibodies against heat shock proteins in environmental stresses and diseases: friend or foe. Cell Stress Chaperon. 11 (2006) 1-12
37. Yamamoto T., McIntyre J., Sell S.M., Georgopoulos C., Skowyra D., and Zylicz M. Enzymology of the pre-priming steps in lambda DNA replication in vitro. J. Biol. Chem. 262 (1987) 7996-7999
38. Yu H., Bao E.-d., Zhao R.-q., and Lv Q.-x. Effect of transportation stress on heat shock protein 70 concentration and mRNA expression in heart and kidney tissues and serum enzyme activities and hormone concentrations of pigs. Am. J. Vet. Res. 68 (2007) 1145-1150