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January 1, 2014World Journal of Nephrology69 citationsOpen Access

Renin-angiotensin system in the kidney: What is new?

FFFernanda M. FerrãoUniversidade Federal do Rio de Janeiro

Key Result

The renin-angiotensin system has paracrine, autocrine, and intracrine functions in the kidney, and new components like the ACE2/Ang-(1-7)/Mas axis offer alternative therapeutic targets for hypertension.

PICO

P
Population
Hypertension and cardiovascular diseases

Abstract

The renin-angiotensin system (RAS) has been known for more than a century as a cascade that regulates body fluid balance and blood pressure. Angiotensin II(Ang II) has many functions in different tissues; however it is on the kidney that this peptide exerts its main functions. New enzymes, alternative routes for Ang IIformation or even active Ang II-derived peptides have now been described acting on Ang II AT1 or AT2 receptors, or in receptors which have recently been cloned, such as Mas and AT4. Another interesting observation was that old members of the RAS, such as angiotensin converting enzyme (ACE), renin and prorenin, well known by its enzymatic activity, can also activate intracellular signaling pathways, acting as an outside-in signal transduction molecule or on the renin/(Pro)renin receptor. Moreover, the endocrine RAS, now is also known to have paracrine, autocrine and intracrine action on different tissues, expressing necessary components for local Ang II formation. This in situ formation, especially in the kidney, increases Ang II levels to regulate blood pressure and renal functions. These discoveries, such as the ACE2/Ang-(1-7)/Mas axis and its antangonistic effect rather than classical deleterious Ang II effects, improves the development of new drugs for treating hypertension and cardiovascular diseases.

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Fernanda M. Ferrão (2014) conducted a review in Hypertension and cardiovascular diseases. The renin-angiotensin system has paracrine, autocrine, and intracrine functions in the kidney, and new components like the ACE2/Ang-(1-7)/Mas axis offer alternative therapeutic targets for hypertension.

synapsesocial.com/papers/6a12894b92637892a9a6c2b8https://doi.org/10.5527/wjn.v3.i3.64
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Renal Uptake of Circulating Angiotensin II in Val5-Angiotensin II Infused Rats Is Mediated by AT1 Receptor1998 · 101 citations
  2. 2Central angiotensin II has catabolic action at white and brown adipose tissue2011 · 74 citations
  3. 3Antihypertensive Effects of Angiotensin Fragments in SHR1995 · 74 citations
  4. 4Intracellular ANG II induces cytosolic Ca2+mobilization by stimulating intracellular AT1receptors in proximal tubule cells2005 · 91 citations
  5. 5Angiotensin-(1-7) Counterregulates Angiotensin II Signaling in Human Endothelial Cells2007 · 284 citations