Literature DB >> 12230267

Interaction of nitric oxide and cell adhesion molecules after 24 hours of complete ureteric obstruction in the rats on a solitary kidney.

H Oztürk1, A I Dokucu, H Buyukbayram.   

Abstract

We aimed to show whether the administration of exogenous L-Arg would alter the morphological, functional changes and interaction of nitric oxide and cell adhesion molecules such as tenascin and lectin after release of twenty-four hours complete ureteric obstruction in the solitary rat kidney tissue. Forty prepubertal Wistar-Albino rats were separated into 4 groups, each containing 10 rats. In the group 1 (Sham-control, n = 10), right nefrectomy was performed; the left ureter was visualized but not ligated. In the remaining 30 rats, the abdomen was opened and undergone right nephrectomy and the left ureter was completely obstructed. After 24 hours, thirty rats were divided as group 2, 3, and 4, each containing 10 rats. In-group 2, no drug treatments were given. In-group 3 L-Arg (L-arginine methyl ester) was infused immediately after abolishing ureteric obstruction. In-group 4 L-NAME was give separately during L-Arg administration during 30 minutes immediately after abolishing ureteric obstruction. Than, the animals were prepared for functional and histopathological studies. BUN value was decreased significantly in L-Arg group when compared with untreatment and L-NAME groups (p < 0.05, p < 0.001 respectively). Creatinine values were decreased in L-Arg group when compared with untreatment group (p < 0.002). Urine flow and urinary Na value was increased significantly in L-Arg group when compared to other obstruction groups (p < 0.001, p < 0.001). The increase in the number of macrophages in Untreated and L-NAME group were significant (p < 0.001, p < 0.001) when compared to L-Arg group. Immunohistochemical study showed that tenascin and lectin expression was severe in tubulus basal membrane of untreated and L-NAME treated rats. In L-Arg group, tenascin and lectin expression was moderate in tubulus membrane. Our results suggest that the administration of exogenous L-Arg protect the functional and degenerative effects of acute complete obstruction in the solitary kidney tissue of the rats. Nitric oxide cause these positive effects by decreasing preglomerular vascular resistance, regulation of neutrophil function and preventing the expression of cell adhesion molecules such as tenascin and lectin.

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Year:  2001        PMID: 12230267     DOI: 10.1023/a:1019515323397

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN: 0301-1623            Impact factor:   2.370


  26 in total

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Authors:  B A Molitoris; J Marrs
Journal:  Am J Med       Date:  1999-05       Impact factor: 4.965

2.  The protective effects of captopril and nitric oxide on solitary kidney after chronic partial ureteric obstruction.

Authors:  H Oztürk; A I Dokucu; S Otçu; A Gezici; A Ketani; F R Yildiz; E Ozdemir; S Yücesan
Journal:  BJU Int       Date:  2001-07       Impact factor: 5.588

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Authors:  A A Reyes; S Klahr
Journal:  Kidney Int       Date:  1992-09       Impact factor: 10.612

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Journal:  Gastroenterology       Date:  1992-08       Impact factor: 22.682

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Journal:  J Am Coll Cardiol       Date:  1993-04       Impact factor: 24.094

Review 7.  The pathophysiology of obstructive nephropathy: the role of vasoactive compounds in the hemodynamic and structural abnormalities of the obstructed kidney.

Authors:  S Klahr; M L Pukerson
Journal:  Am J Kidney Dis       Date:  1994-02       Impact factor: 8.860

Review 8.  The role of neutrophils in acute renal failure.

Authors:  S Lauriat; S L Linas
Journal:  Semin Nephrol       Date:  1998-09       Impact factor: 5.299

9.  Soluble L-selectin is present in human plasma at high levels and retains functional activity.

Authors:  B Schleiffenbaum; O Spertini; T F Tedder
Journal:  J Cell Biol       Date:  1992-10       Impact factor: 10.539

10.  Induction of tenascin in healing wounds.

Authors:  E J Mackie; W Halfter; D Liverani
Journal:  J Cell Biol       Date:  1988-12       Impact factor: 10.539

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