This review considers molecular mechanisms that underlie disorders in the s
tructure and metabolism of renal extracellular matrix in diabetic nephropat
hy. The contribution of the increased synthesis of renal extracellular matr
ix proteins in the accumulation of renal mesangial matrix is considered, an
d the important role of the degradation system of the extracellular matrix
proteins in the development of fibrosis is also shown. Data on changes in m
RNA expression for the matrix metalloproteinases (MMP) and tissue inhibitor
s of metalloproteinases (TIMP) in various forms of diabetic nephropathy are
presented. A correlation is established between changes in the balance of
MMP proteolytic activity and TIMP activity and the accumulation of extracel
lular matrix.