FUNCTIONAL AND HISTOLOGIC ALTERATIONS IN GROWING SOLITARY RAT-KIDNEY AS RESULT OF EXTRACORPOREAL SHOCKWAVES

Citation
U. Ferreira et al., FUNCTIONAL AND HISTOLOGIC ALTERATIONS IN GROWING SOLITARY RAT-KIDNEY AS RESULT OF EXTRACORPOREAL SHOCKWAVES, Journal of endourology, 9(1), 1995, pp. 45-49
Citations number
24
Categorie Soggetti
Urology & Nephrology
Journal title
ISSN journal
08927790
Volume
9
Issue
1
Year of publication
1995
Pages
45 - 49
Database
ISI
SICI code
0892-7790(1995)9:1<45:FAHAIG>2.0.ZU;2-6
Abstract
The long-term effects of extracorporeal shockwave lithotripsy (SWL) on children treated for renal calculi are unclear. To study the effects on the immature animal, we evaluated 31 Wistar white rats that underwe nt right nephrectomy at 30 days of age. At 40 days of age they were di vided into three groups: a control group of 10 rats that received no s hockwaves; Group I (9 rats) that received 1000 shockwaves at 16.0 kV, and Group II (12 animals) that received 1000 shock waves at 17.2 kV. S ix months later at maturity (7 months and 10 days of age), the followi ng parameters were measured: (1) body and renal weight; (2) blood lith ium, sodium, potassium, and creatinine; (3) fractional lithium, sodium , and potassium excretion; and (4) clearances of lithium and creatinin e. The kidneys were studied grossly and histologically. We found no si gnificant changes in overall animal and renal growth between the post- SWL and control groups. However, there were significant changes in ren al function. The animals in Groups I and II presented significant incr eases in blood potassium compared with the control group. Furthermore, the 1000 x 17.2 kV group showed permanent histologic renal changes, i ncluding red cells in Bowman's capsule and glomerular congestion. The disorders caused by SWL are compatible with hyporeninemic hypoaldoster onism, inappropriately low plasma renin activity, and aldosterone defi ciency. We conclude that although SWL does not affect either overall o r renal growth, it may cause significant changes in renal function and permanent histologic damage.