Lai, 2000), cortical levels were higher in the present study in the obese Zucker rat as well as in a study by Yabuki et al. in the Long Evans Tokushima Fatty rat (Yabuki, Tahara, 2006). This may reflect pathophysiological differences specific to the type of PD150606 structure diabetes or to the comorbid obesity, or an inability of the Zucker rat to mount an adequate compensatory nNOS response in the medulla. Li et al. previously reported that this rat model can exhibit downregulation of nNOS in the setting of tubular damage preceding frank diabetes and renal failure (Li et al., 2005). Few studies have been done on the effects of diabetes on nNOS in kidneys of female rats. In the present study, overall nNOS expression was lower in females than in males. This may be indicative of a sex difference in the degree of tubular inflammation and damage or due to the known effects of sex steroids on the pathogenesis of renal disease, including cellActa Histochem. Author manuscript; available in PMC 2017 March 01.Author Manuscript Author Manuscript Author Manuscript Author ManuscriptSlyvka et al.Pageproliferation, synthesis and degradation of collagen and proteoglycans and oxidative balance (Neugarten et al., 1997). Androgens can increase levels of damaging superoxide in the kidney (Iliescu et al., 2007). Estrogens increase endogenous antioxidant activity and suppress collagen synthesis in glomerular mesangial cells (Kwan et al., 1996). These hormonal effects may evoke a more modest induction of nNOS in females than that seen in males. 4.4 iNOS iNOS is not found in significant amounts in healthy kidney (Jarry, Renaudin, 2003, Romagnani et al., 1999). However, as shown here, iNOS is expressed in aging or damaged kidneys, including DN, in proximal and distal tubules and both cortical and medullary collecting ducts (Cosenzi, Bernobich, 2002, Fujihara, Mattar, 2002, Liang et al., 2010, Ptilovanciv, Fernandes, 2013, Veelken, Hilgers, 2000). iNOS has also been observed in glomerular epithelial and mesangial cells of diabetic rats and humans and the intensity and extent of staining increase with severity of nephropathy (Hohenstein, Hugo, 2008, Jeong et al., 2009, Moon et al., 2011). iNOS null mice demonstrate increased mesangial hypercellularity and expansion as well as more prominent tubulo-interstitial fibrosis (Trachtman et al., 2002). However, iNOS was not detected in glomeruli in the present study, possibly due to differences in species, purchase SC144 strain or treatment. There were no sex differences in iNOS in rats on a REG diet. However, provision of an AOfortified diet resulted in increased iNOS in kidney of diabetic Zucker male rats at 6 weeks, but not in female rats. The effects of iNOS in the injured kidney remain controversial. Low levels of compensatory NO production by iNOS may be beneficial, especially early in the disease process, by increasing vasodilatory [NO] and inducing Cu/Zn superoxide dismutase (Alderton, Cooper, 2001, Pfeilschifter et al., 2003). With continued exposure to NO generated by iNOS and ROS generation by NOS monomers, which increase in DM due to dissociation of dimers (Slyvka, Wang, 2011), NO chemistry shifts towards harmful effects such as nitrosylation, nitration and oxidation (Alderton, Cooper, 2001, Brune, 2002, Pfeilschifter et al., 2001). ROS and reactive nitrogen species (RNS) are harmful to the kidney (Droge, 2002, Tan, Forbes, 2007, van der Vliet et al., 1996) and increased nitrosative and oxidative stress is one of the leading mechanisms in.Lai, 2000), cortical levels were higher in the present study in the obese Zucker rat as well as in a study by Yabuki et al. in the Long Evans Tokushima Fatty rat (Yabuki, Tahara, 2006). This may reflect pathophysiological differences specific to the type of diabetes or to the comorbid obesity, or an inability of the Zucker rat to mount an adequate compensatory nNOS response in the medulla. Li et al. previously reported that this rat model can exhibit downregulation of nNOS in the setting of tubular damage preceding frank diabetes and renal failure (Li et al., 2005). Few studies have been done on the effects of diabetes on nNOS in kidneys of female rats. In the present study, overall nNOS expression was lower in females than in males. This may be indicative of a sex difference in the degree of tubular inflammation and damage or due to the known effects of sex steroids on the pathogenesis of renal disease, including cellActa Histochem. Author manuscript; available in PMC 2017 March 01.Author Manuscript Author Manuscript Author Manuscript Author ManuscriptSlyvka et al.Pageproliferation, synthesis and degradation of collagen and proteoglycans and oxidative balance (Neugarten et al., 1997). Androgens can increase levels of damaging superoxide in the kidney (Iliescu et al., 2007). Estrogens increase endogenous antioxidant activity and suppress collagen synthesis in glomerular mesangial cells (Kwan et al., 1996). These hormonal effects may evoke a more modest induction of nNOS in females than that seen in males. 4.4 iNOS iNOS is not found in significant amounts in healthy kidney (Jarry, Renaudin, 2003, Romagnani et al., 1999). However, as shown here, iNOS is expressed in aging or damaged kidneys, including DN, in proximal and distal tubules and both cortical and medullary collecting ducts (Cosenzi, Bernobich, 2002, Fujihara, Mattar, 2002, Liang et al., 2010, Ptilovanciv, Fernandes, 2013, Veelken, Hilgers, 2000). iNOS has also been observed in glomerular epithelial and mesangial cells of diabetic rats and humans and the intensity and extent of staining increase with severity of nephropathy (Hohenstein, Hugo, 2008, Jeong et al., 2009, Moon et al., 2011). iNOS null mice demonstrate increased mesangial hypercellularity and expansion as well as more prominent tubulo-interstitial fibrosis (Trachtman et al., 2002). However, iNOS was not detected in glomeruli in the present study, possibly due to differences in species, strain or treatment. There were no sex differences in iNOS in rats on a REG diet. However, provision of an AOfortified diet resulted in increased iNOS in kidney of diabetic Zucker male rats at 6 weeks, but not in female rats. The effects of iNOS in the injured kidney remain controversial. Low levels of compensatory NO production by iNOS may be beneficial, especially early in the disease process, by increasing vasodilatory [NO] and inducing Cu/Zn superoxide dismutase (Alderton, Cooper, 2001, Pfeilschifter et al., 2003). With continued exposure to NO generated by iNOS and ROS generation by NOS monomers, which increase in DM due to dissociation of dimers (Slyvka, Wang, 2011), NO chemistry shifts towards harmful effects such as nitrosylation, nitration and oxidation (Alderton, Cooper, 2001, Brune, 2002, Pfeilschifter et al., 2001). ROS and reactive nitrogen species (RNS) are harmful to the kidney (Droge, 2002, Tan, Forbes, 2007, van der Vliet et al., 1996) and increased nitrosative and oxidative stress is one of the leading mechanisms in.
