Pre-exposure to heat shock inhibits peroxynitrite-induced activation of poly(ADP) ribosyltransferase and protects against peroxynitrite cytotoxicity in J774 macrophages
References (39)
- et al.
Characterization of the cellular reduction of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT): subcellular localization, substrate dependence, and involvement of mitochondrial electron transport in MTT reduction
Arch. Biochem. Biophys.
(1993) - et al.
The comparative toxicity of nitric oxide and peroxynitrite to Escherichia coli
(1995) - et al.
Suppression of nitric oxide toxicity in islet cells by alpha-tocopherol
FEBS Lett.
(1995) - et al.
Aconitase is readily inactivated by peroxynitrite, but not by its precursor, nitric oxide
J. Biol. Chem.
(1994) - et al.
Superoxide and peroxynitrite inactivate aconitases, but nitric oxide does not
J. Biol. Chem.
(1994) - et al.
DNA damage induced by simultaneous generation of nitric oxide and superoxide
FEBS Lett.
(1995) - et al.
Heat shock induces peroxidase activity in Neurospora crassa and confers tolerance toward oxidative stress
Biochem. Biophys. Res. Commun.
(1987) - et al.
Evidence for nitric oxide-mediated oxidative damage in chronic inflammation; nitrotyrosine in serum and synovial fluid from rheumatoid patients
FEBS Lett.
(1994) - et al.
Role of inducible nitric oxide synthase expression and peroxynitrite formation in guinea pig ileitis
Gastroenterology
(1995) - et al.
Peroxynitrite-induced membrane lipid peroxidation: the cytotoxic potential of superoxide and nitric oxide
Arch. Biochem. Biophys.
(1991)
DNA damage and oxidation of thiols peroxynitrite causes in rat thymocytes
Arch. Biochem. Biophys.
The formation of peroxynitrite in vivo from nitric oxide and superoxide
Chem.-Biol. Interact.
Endogenous peroxynitrite is involved in the inhibition of cellular respiration in immuno-stimulated J774.2 macrophages
Biochem. Biophys. Res. Commun.
Endotoxin triggers the expression of an inducible isoform of nitric oxide synthase and the formation of peroxynitrite in the rat aorta in vivo
FEBS Lett.
Peroxynitrite-mediated oxidation of dihydrorhodamine 123 occurs in early stages of endotoxic and hemorrhagic shock and ischemia-reperfusion injury
FEBS Lett.
Heat shock induces resistance in rat pancreatic islet cells against nitric oxide, oxygen radicals and streptozotocin toxicity in vitro
J. Clin. Invest.
Nitric oxide: role in neurotoxicity
Clin. Exp. Pharmacol. Physiol.
Autocrine inhibition of Na + /K(+)-ATPase by nitric oxide in mouse proximal tubule epithelial cells
J. Clin. Invest.
Peroxynitrite inhibition of oxygen consumption and sodium transport in alveolar type II cells
Am. J. Physiol.
Cited by (21)
Anti-apoptotic and Anti-inflammatory effect of Piperine on 6-OHDA induced Parkinson's Rat model
2013, Journal of Nutritional BiochemistryCitation Excerpt :Another parameter we studied for apoptosis is Poly (ADP-ribose) polymerase (PARP). Under physiological conditions, PARP is constitutively activated at low levels and plays a role in housekeeping DNA repair functions, such as base excision repair [33,34]. Under pathological conditions, however, wherein DNA damage is excessive, PARP is over-activated.
Melatonin: A hormone that modulates pain
2009, Life SciencesHeat shock response and acute lung injury
2007, Free Radical Biology and MedicineNew insights on brain stem death: From bedside to bench
2005, Progress in NeurobiologyCitation Excerpt :Mediation of the cytotoxic cardiovascular actions of NO by peroxynitrite (ONOO−), a potent reactive oxidant formed by the reaction between superoxide anion (O2−) and NO was also reported (Blough and Zafiriou, 1985; Beckman et al., 1990; Garcia-Estan et al., 2002). In vascular tissues, the formation of peroxynitrite during circulatory shock (Szabo et al., 1995, 1996; Fukuyama et al., 1997) and stroke (Oury et al., 1993) is consistent with the notion that some of the pathological alterations attributed previously to NO are consequences of peroxynitrite actions. It is thus of interest to note that these two signaling cascades are differentially associated with the concentration-dependent bi-directional modulation of glutamatergic neurotransmission by NO on RVLM neurons.
Cardioprotective effects of poly(ADP-ribose) polymerase inhibition
2005, Pharmacological Research