Protein Information

ID 2122
Name hypoxia inducible factor 1alpha
Synonyms ARNT interacting protein; HIF 1 alpha; HIF 1alpha; HIF1 alpha; HIF1A; Hypoxia inducible factor 1 alpha subunit; Hypoxia inducible factor 1 alpha; Hypoxia inducible factor 1alpha…

Compound Information

ID 954
Name SMA
CAS sodium 2-chloroacetate

Reference

PubMed Abstract RScore(About this table)
20232302 Roson MI, Della Penna SL, Cao G, Gorzalczany S, Pandolfo M, Toblli JE, Fernandez BE: Different protective actions of losartan and tempol on the renal inflammatory response to acute sodium overload. J Cell Physiol. 2010 Mar 15.
The aim of this work was to study the role of local intrarenal angiotensin II (Ang II) and the oxidative stress in the up-regulation of pro-inflammatory cytokines expression observed in rats submitted to an acute sodium overload. Sprague-Dawley rats were infused for 2 h with isotonic saline solution (Control group) and with hypertonic saline solution alone (Na group), plus the AT1 receptor antagonist losartan (10 mg kg (-1) in bolus) (Na-Los group), or plus the superoxide dismutase mimetic tempol (0.5 mg min (-1) kg (-1)) (Na-Temp group). Mean arterial pressure, glomerular filtration rate, and fractional sodium excretion (FE (Na)) were measured. Ang II, NF-kappaB, hypoxia inducible factor-1alpha (HIF-1alpha), transforming growth factor beta1 (TGF-beta1), smooth muscle actin (alpha-SMA), endothelial nitric oxide synthase (eNOS), and RANTES renal expression was evaluated by immunohistochemistry. Ang II, NF-kappaB, and TGF-beta1 and RANTES early inflammatory markers were overexpressed in Na group, accompanied by enhanced HIF-1alpha immunostaining, lower eNOS expression, and unmodified alpha-SMA. Losartan and tempol increased FE (Na) in sodium overload group. Although losartan reduced Ang II and NF-kappaB staining and increased eNOS expression, it did not restore HIF-1alpha expression and did not prevent inflammation. Conversely, tempol increased eNOS and natriuresis, restored HIF-1alpha expression, and prevented inflammation. Early inflammatory markers observed in rats with acute sodium overload is associated with the imbalance between HIF-1alpha and eNOS expression. While both losartan and tempol increased natriuresis and eNOS expression, only tempol was effective in restoring HIF-1alpha expression and down-regulating TGF-beta1 and RANTES expression. The protective role of tempol, but not of losartan, in the inflammatory response may be associated with its greater antioxidant effects. J. Cell. Physiol. (c) 2010 Wiley-Liss, Inc.
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