scholarly journals The reactive nitrogen species peroxynitrite is a potent inhibitor of renal Na-K-ATPase activity

2008 ◽  
Vol 295 (4) ◽  
pp. F1191-F1198 ◽  
Author(s):  
Matthew S. Reifenberger ◽  
Krista L. Arnett ◽  
Craig Gatto ◽  
Mark A. Milanick

Peroxynitrite is a reactive nitrogen species produced when nitric oxide and superoxide react. In vivo studies suggest that reactive oxygen species and, perhaps, peroxynitrite can influence Na-K-ATPase function. However, the direct effects of peroxynitrite on Na-K-ATPase function remain unknown. We show that a single bolus addition of peroxynitrite inhibited purified renal Na-K-ATPase activity, with IC50 of 107 ± 9 μM. To mimic cellular/physiological production of peroxynitrite, a syringe pump was used to slowly release (∼0.85 μM/s) peroxynitrite. The inhibition of Na-K-ATPase activity induced by this treatment was similar to that induced by a single bolus addition of equal cumulative concentration. Peroxynitrite produced 3-nitrotyrosine residues on the α, β, and FXYD subunits of the Na pump. Interestingly, the flavonoid epicatechin, which prevented tyrosine nitration, was unable to blunt peroxynitrite-induced ATPase inhibition, suggesting that tyrosine nitration is not required for inhibition. Peroxynitrite led to a decrease in iodoacetamidofluorescein labeling, implying that cysteine modifications were induced. Glutathione was unable to reverse ATPase inhibition. The presence of Na+ and low MgATP during peroxynitrite treatment increased the IC50 to 145 ± 10 μM, while the presence of K+ and low MgATP increased the IC50 to 255 ± 13 μM. This result suggests that the EPNa conformation of the pump is slightly more sensitive to peroxynitrite than the E(K) conformation. Taken together, these results show that peroxynitrite is a potent inhibitor of Na-K-ATPase activity and that peroxynitrite can induce amino acid modifications to the pump.

2008 ◽  
Vol 283 (29) ◽  
pp. 20186-20197 ◽  
Author(s):  
Hyoung Chul Choi ◽  
Ping Song ◽  
Zhonglin Xie ◽  
Yong Wu ◽  
Jian Xu ◽  
...  

2019 ◽  
Vol 294 (27) ◽  
pp. 10742-10742
Author(s):  
Hyoung Chul Choi ◽  
Ping Son ◽  
Zhonglin Xie ◽  
Yong Wu ◽  
Jian Xu ◽  
...  

2003 ◽  
Vol 374 (2) ◽  
pp. 521-527 ◽  
Author(s):  
Ali R. MANI ◽  
Ananth S. PANNALA ◽  
Nelson N. ORIE ◽  
Richard OLLOSSON ◽  
David HARRY ◽  
...  

Reactive nitrogen species, such as peroxynitrite, can nitrate tyrosine in proteins to form nitrotyrosine. Nitrotyrosine is metabolized to 3-nitro-4-hydroxyphenylacetic acid (NHPA), which is excreted in the urine. This has led to the notion that measurement of urinary NHPA may provide a time-integrated index of nitrotyrosine formation in vivo. However, it is not known whether NHPA is derived exclusively from metabolism of nitrotyrosine, or whether it can be formed by nitration of circulating para-hydroxyphenylacetic acid (PHPA), a metabolite of tyrosine. In the present study, we have developed a gas chromatography MS assay for NHPA and PHPA to determine whether or not NHPA can be formed directly by nitration of PHPA. Following the injection of nitrotyrosine, 0.5±0.16% of injected dose was recovered unchanged as nitrotyrosine, and 4.3±0.2% as NHPA in the urine. To determine whether or not NHPA could be formed by the nitration of PHPA, deuterium-labelled PHPA ([2H6]PHPA) was injected, and the formation of deuterated NHPA ([2H5]NHPA) was measured. Of the infused [2H6]PHPA, 78±2% was recovered in the urine unchanged, and approx. 0.23% was recovered as [2H5]NHPA. Since the plasma concentration of PHPA is markedly higher than free nitrotyrosine (approx. 400-fold), the nitration of high-circulating endogenous PHPA to form NHPA becomes very significant and accounts for the majority of NHPA excreted in urine. This is the first study to demonstrate that NHPA can be formed by nitration of PHPA in vivo, and that this is the major route for its formation.


2019 ◽  
Vol 294 (36) ◽  
pp. 13525-13525 ◽  
Author(s):  
Ming-Hui Zou ◽  
Stacy S. Kirkpatrick ◽  
Bradley J. Davis ◽  
John S. Nelson ◽  
Walger G. Wiles ◽  
...  

2020 ◽  
Vol 8 (6) ◽  
pp. 980-992
Author(s):  
Julian G. Bonetto ◽  
◽  
Juan C. Perazzo ◽  
Susana Puntarulo ◽  
◽  
...  

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