Sn. Emancipator et al., ORAL ENZYMES IN DIFFERENT ANIMAL-MODELS OF GLOMERULONEPHRITIS, International journal of immunotherapy, 13(3-4), 1997, pp. 97-103
Systemic or oral proteolytic enzymes ameliorate any of several glomeru
lonephritides in mice, rats or rabbits. Recently in rats with membrano
us nephropathy induced by cationized antigen, oral Phlogenzym(R) thera
py progressively diminished proteinuria and hyperlipidemia (ultimately
by 50%) over a 2-week period, whereas untreated diseased controls sho
wed stable and sustained proteinuria and hyperlipidemia. At sacrifice,
the amount of glomerular immune deposits, assessed by semiquantitativ
e immunofluorescence and quantitative electron microscopy were 45% of
the amount in controls. Moreover when this model was sustained for 7 m
onths, glomerulosclerosis involved an average of approximately 80% oi
the glomeruli in untreated rats with nephrosis; whereas two different
preparations of proteolytic enzymes, given intraperitoneally: had a si
gnificant sparing effect on glomeruli. Only 25% of the glomeruli from
rats in either protease-treated group appeared sclerotic, as compared
to 12% in nondiseased age-matched controls. We conclude that enzyme th
erapy diminishes the clinical signs and morphologic lesions of immune
complex glomerulonephritis; reduces ?he immune deposits, and, prevents
or retards the progression to end stage renal disease.