Title : Hypoxia inducible factor-1α-mediated gene activation in the regulation of renal medullary function and salt sensitivity of blood pressure.

Pub. Date : 2012

PMID : 22937490






10 Functional Relationships(s)
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1 High salt intake suppresses the expression of PHD2 in the renal medulla, which increases HIF-1alpha-mediated gene expressions in the renal medulla, thereby participates in the control of salt sensitivity of blood pressure. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
2 High salt intake suppresses the expression of PHD2 in the renal medulla, which increases HIF-1alpha-mediated gene expressions in the renal medulla, thereby participates in the control of salt sensitivity of blood pressure. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
3 3) The high salt-induced inhibition in PHD2 and the consequent activation of HIF-1alpha in the renal medulla is not observed in Dahl salt sensitive hypertensive (Dahl/ss) rats. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
4 Correction of these defects in PHD2/HIF-1alpha-associated molecular adaptation in the renal medulla improves sodium excretion, reduces sodium retention and attenuates saltsensitive hypertension in Dahl/ss rats. Sodium egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
5 Correction of these defects in PHD2/HIF-1alpha-associated molecular adaptation in the renal medulla improves sodium excretion, reduces sodium retention and attenuates saltsensitive hypertension in Dahl/ss rats. Sodium egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
6 In conclusion, PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla is an important molecular adaptation to high salt intake; impaired PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla may be responsible for the salt-sensitive hypertension in Dahl/ss rats; correction of these defects may be used to as therapeutic strategies for the treatment of salt-sensitive hypertension. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
7 In conclusion, PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla is an important molecular adaptation to high salt intake; impaired PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla may be responsible for the salt-sensitive hypertension in Dahl/ss rats; correction of these defects may be used to as therapeutic strategies for the treatment of salt-sensitive hypertension. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
8 In conclusion, PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla is an important molecular adaptation to high salt intake; impaired PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla may be responsible for the salt-sensitive hypertension in Dahl/ss rats; correction of these defects may be used to as therapeutic strategies for the treatment of salt-sensitive hypertension. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
9 In conclusion, PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla is an important molecular adaptation to high salt intake; impaired PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla may be responsible for the salt-sensitive hypertension in Dahl/ss rats; correction of these defects may be used to as therapeutic strategies for the treatment of salt-sensitive hypertension. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus
10 In conclusion, PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla is an important molecular adaptation to high salt intake; impaired PHD2 regulation of HIF-1alpha-mediated gene activation in the renal medulla may be responsible for the salt-sensitive hypertension in Dahl/ss rats; correction of these defects may be used to as therapeutic strategies for the treatment of salt-sensitive hypertension. Salts egl-9 family hypoxia-inducible factor 1 Rattus norvegicus