TY - JOUR
T1 - Regulation of vascular smooth muscle cell growth by aldose reductase
AU - Bhatnagar, Aruni
AU - Ruef, Johannes
AU - Liu, Si Qi
AU - Srivastava, Sanjay
AU - Srivastava, Satish K.
N1 - Funding Information:
This work was supported in part by NIH grants HL55477 and HL59378 (A.B.); a grant from the American Heart Association–Ohio Valley Affiliate (S.Q.L.) and a research scholarship Ru 620/1-1 from the German Research Foundation DFG (J.R.).
PY - 2001/1/30
Y1 - 2001/1/30
N2 - Aldose reductase (AR) is a broad-specificity aldo-keto reductase with wide species and tissue distribution. The enzyme has been implicated in the development of pleiotropic complications of long-term diabetes. However, the euglycemic function of the enzyme remains unclear. To examine its potential role in cell growth, changes in AR mRNA and protein were measured in human aortic smooth muscle cells exposed in culture to serum or thrombin. Stimulation by these mitogens led to an increase in the abundance of AR mRNA and protein. Furthermore, inhibition of the AR by tolrestat and sorbinil diminished DNA synthesis and cell proliferation in response to serum. Immunohistochemical staining with anti-AR antibodies revealed no significant expression of AR in the smooth muscle cells of rat carotid arteries. However, 10 and 21 days after balloon injury, intense staining was associated with the proliferating cells of the neointima. Treatment of these animals with 40 mg/kg/day sorbinil diminished the ratio of neointima to the media. Together, these observations suggest that, in vascular smooth muscle cells (VSMC), AR is a growth-responsive gene product and that inhibition of AR prevents VSMC growth and decreases intimal hyperplasia and restenosis.
AB - Aldose reductase (AR) is a broad-specificity aldo-keto reductase with wide species and tissue distribution. The enzyme has been implicated in the development of pleiotropic complications of long-term diabetes. However, the euglycemic function of the enzyme remains unclear. To examine its potential role in cell growth, changes in AR mRNA and protein were measured in human aortic smooth muscle cells exposed in culture to serum or thrombin. Stimulation by these mitogens led to an increase in the abundance of AR mRNA and protein. Furthermore, inhibition of the AR by tolrestat and sorbinil diminished DNA synthesis and cell proliferation in response to serum. Immunohistochemical staining with anti-AR antibodies revealed no significant expression of AR in the smooth muscle cells of rat carotid arteries. However, 10 and 21 days after balloon injury, intense staining was associated with the proliferating cells of the neointima. Treatment of these animals with 40 mg/kg/day sorbinil diminished the ratio of neointima to the media. Together, these observations suggest that, in vascular smooth muscle cells (VSMC), AR is a growth-responsive gene product and that inhibition of AR prevents VSMC growth and decreases intimal hyperplasia and restenosis.
KW - Aldose reductase
KW - Rat carotid artery
KW - Restenosis
KW - Vascular smooth muscle cells
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U2 - 10.1016/S0009-2797(00)00290-8
DO - 10.1016/S0009-2797(00)00290-8
M3 - Article
C2 - 11306081
AN - SCOPUS:0035969858
SN - 0009-2797
VL - 130-132
SP - 627
EP - 636
JO - Chemico-Biological Interactions
JF - Chemico-Biological Interactions
ER -