Light and Electron Microscopic localization of inducible nitric oxide synthase in the heart of rats with myocarditis

Author(s):  
T. Nishikawa ◽  
S. Ishiyama ◽  
K. Takeda ◽  
T. Shimojo ◽  
M. Hiroe ◽  
...  

Nitric oxide synthase (NOS) is an enzyme involved in the synthesis of nitric oxide (NO). The inducible form of NOS (iNOS) is induced in the presence of cytokines and produces massive amounts of NO which may be harmful to living tissue. In acute myocarditis, a serious disease which can be fatal, extensive myocardial cell damage associated with massive inflammatory cell infiltration is usually observed and large amounts of cytokines are released from inflammatory cells. However, the mechanism of the heart tissue injury is still unclear. In this study, we investigated the role of iNOS in the myocardial tissue injury in acute myocarditis.The heart tissue specimens were taken from Lewis rats with experimentally induced autoimmune myocarditis. An immunohistochemical study was performed using iNOS antibody raised in New Zealand white rabbits immunized with synthetic peptides (17 amino acids) corresponding to the C-terminal of macrophage iNOS. The specificity of the antibody was confirmed by Western blot analysis. Immunoelectron microscopic studies were carried out by the gold-labeled IgG method using ultrathin sections of LR white resin-embedded material.

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Mohamed A. Morsy ◽  
Salwa A. Ibrahim ◽  
Entesar F. Amin ◽  
Maha Y. Kamel ◽  
Rehab A. Rifaai ◽  
...  

Gentamicin, an aminoglycoside antibiotic, is used for the treatment of serious Gram-negative infections. However, its usefulness is limited by its nephrotoxicity. Sildenafil, a selective phosphodiesterase-5 inhibitor, was reported to prevent or decrease tissue injury. The aim of this study is to evaluate the potential protective effects of sildenafil on gentamicin-induced nephrotoxicity in rats. Male Wistar rats were injected with gentamicin (100 mg/kg/day, i.p.) for 6 days with and without sildenafil. Sildenafil administration resulted in nephroprotective effect in gentamicin-intoxicated rats as it significantly decreased serum creatinine and urea, urinary albumin, and renal malondialdehyde and nitrite/nitrate levels, with a concomitant increase in renal catalase and superoxide dismutase activities compared to gentamicin-treated rats. Moreover, immunohistochemical examination revealed that sildenafil treatment markedly reduced inducible nitric oxide synthase (iNOS) expression, while expression of endothelial nitric oxide synthase (eNOS) was markedly enhanced. The protective effects of sildenafil were verified histopathologically. In conclusion, sildenafil protects rats against gentamicin-induced nephrotoxicity possibly, in part, through its antioxidant activity, inhibition of iNOS expression, and induction of eNOS production.


1993 ◽  
Vol 38 (S2) ◽  
pp. C125-C126 ◽  
Author(s):  
N. K. Boughton-Smith ◽  
S. M. Evans ◽  
B. J. R. Whittle ◽  
S. Moncada

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