Thermal preconditioning before rat arterial balloon injury: limitation of injury and sustained reduction of intimal thickening.

Heat shock proteins (HSPs) are a family of highly conserved proteins, essential to cell survival, that are induced during times of physiological stress. These proteins, when induced, can provide tolerance to subsequent injury. Several studies have documented that HSPs play an important role in the response of vascular cells to injury or stress. Whether the vasculature itself can be effectively preconditioned before arterial injury is unknown. Vascular HSP induction by whole-body hyperthermia (WBH) was evaluated with regard to its effects on the vascular response to balloon injury. WBH treatment of Sprague-Dawley rats (colonic temperatures of 41 to 42 degrees C for 15 minutes) resulted in maximal arterial HSP expression within 8 to 12 hours. Rats (male, 300 g, n=59) were randomly assigned to undergo either WBH or no treatment 8 hours before standard carotid balloon injury. At 14 (n=26) and 90 (n=21) days after balloon injury, histomorphometric analysis revealed a significant limitation of intimal accumulation in preconditioned arteries as compared to controls (intimal/medial area ratios+/-SEM: 14 days, 0.57+/-0.07 versus 0.86+/-0.08, P=0.01; 90 days, 0.78+/-0.12 versus 1.19+/-0.14, P<0.05). The medial cell proliferation index at 4 days (n=12) was significantly reduced in the treated group as well (3.6+/-0.9% versus 7.2+/-1.3%, P<0.05). Conversely, the mean total cell number in the media of heated arteries was higher (393+/-20 versus 328+/-17, P<0.05). Vascular preconditioning with brief WBH induces a heat shock response in the arterial wall that is associated with a significant and sustained reduction in intimal accumulation. This effect appears to be due in part to preservation of medial cell integrity and limitation of the proliferative response. These results suggest that thermal preconditioning of vascular tissue may be an effective strategy to improve long-term results after revascularization procedures.

[1]  T. Maciag,et al.  A Carboxyl-terminal Domain in Fibroblast Growth Factor (FGF)-2 Inhibits FGF-1 Release in Response to Heat Shock in Vitro* , 1997, The Journal of Biological Chemistry.

[2]  Y. Yamaoka,et al.  Protective effect of heat shock pretreatment with heat shock protein induction before hepatic warm ischemic injury caused by Pringle's maneuver. , 1995, Surgery.

[3]  M. Condorelli,et al.  Smooth muscle cell proliferation is proportional to the degree of balloon injury in a rat model of angioplasty. , 1995, Circulation.

[4]  Qingbo Xu,et al.  Acute hypertension induces heat-shock protein 70 gene expression in rat aorta. , 1995, Circulation.

[5]  G. Kollias,et al.  Transgenic mice expressing the human heat shock protein 70 have improved post-ischemic myocardial recovery. , 1995, The Journal of clinical investigation.

[6]  D. Scharp,et al.  Heat shock and recovery protects pancreatic islets from warm ischemic injury. , 1994, Transplantation proceedings.

[7]  W Rutsch,et al.  A comparison of balloon-expandable-stent implantation with balloon angioplasty in patients with coronary artery disease. Benestent Study Group. , 1994, The New England journal of medicine.

[8]  E. Nabel,et al.  Gene therapy for vascular smooth muscle cell proliferation after arterial injury. , 1994, Science.

[9]  R. Mestril,et al.  Isolation of a novel inducible rat heat-shock protein (HSP70) gene and its expression during ischaemia/hypoxia and heat shock. , 1994, The Biochemical journal.

[10]  D. Faxon,et al.  Prevention of Post‐PTCA Restenosis , 1994, Annals of the New York Academy of Sciences.

[11]  D. Ricci,et al.  A comparison of directional atherectomy with balloon angioplasty for lesions of the left anterior descending coronary artery. , 1993, The New England journal of medicine.

[12]  R. Califf,et al.  A Comparison of Directional Atherectomy with Coronary Angioplasty in Patients with Coronary Artery Disease , 1993 .

[13]  E. Nabel,et al.  Recombinant fibroblast growth factor-1 promotes intimal hyperplasia and angiogenesis in arteries in vivo , 1993, Nature.

[14]  N. Holbrook,et al.  Vascular heat shock protein expression in response to stress. Endocrine and autonomic regulation of this age-dependent response. , 1993, The Journal of clinical investigation.

[15]  R. Ferrari,et al.  The protective role of heat stress in the ischaemic and reperfused rabbit myocardium. , 1992, Journal of molecular and cellular cardiology.

[16]  L. Weber Relationship of heat shock proteins and induced thermal resistance , 1992, Cell proliferation.

[17]  M. Reidy,et al.  Proliferation of smooth muscle cells after vascular injury is inhibited by an antibody against basic fibroblast growth factor. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[18]  G. Li,et al.  Thermal response of rat fibroblasts stably transfected with the human 70-kDa heat shock protein-encoding gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[19]  M. Bond,et al.  Effect of heat shock proteins on survival of isolated aortic cells from normal and atherosclerotic cynomolgus macaques. , 1990, Atherosclerosis.

[20]  M. Fishman,et al.  Heat shock protects pig kidneys against warm ischemic injury. , 1990, Transplantation proceedings.

[21]  K. Riabowol,et al.  Heat shock is lethal to fibroblasts microinjected with antibodies against hsp70. , 1988, Science.

[22]  W. Welch,et al.  Characterization of the thermotolerant cell. I. Effects on protein synthesis activity and the regulation of heat-shock protein 70 expression , 1988, The Journal of cell biology.

[23]  F. Bosman,et al.  Effect of tissue fixation on anti-bromodeoxyuridine immunohistochemistry. , 1987, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[24]  M. Reidy,et al.  Kinetics of cellular proliferation after arterial injury. I. Smooth muscle growth in the absence of endothelium. , 1983, Laboratory investigation; a journal of technical methods and pathology.

[25]  A. Tissières,et al.  Protein synthesis in salivary glands of Drosophila melanogaster: relation to chromosome puffs. , 1974, Journal of molecular biology.

[26]  M. Bond,et al.  Differential distribution of 70-kD heat shock protein in atherosclerosis. Its potential role in arterial SMC survival. , 1995, Arteriosclerosis, thrombosis, and vascular biology.

[27]  E. Craig,et al.  Heat-shock proteins as molecular chaperones. , 1994, European journal of biochemistry.

[28]  P. Teirstein,et al.  A randomized comparison of coronary-stent placement and balloon angioplasty in the treatment of coronary artery disease. Stent Restenosis Study Investigators. , 1994, The New England journal of medicine.

[29]  G. Church,et al.  Genomic sequencing. , 1993, Methods in molecular biology.

[30]  M. Reidy,et al.  Role of basic fibroblast growth factor in vascular lesion formation. , 1991, Circulation research.

[31]  M. Bond,et al.  Immunohistochemical localization of heat shock protein-70 in normal-appearing and atherosclerotic specimens of human arteries. , 1990, The American journal of pathology.