Adenosine A(2A) and A(3) Receptors as Targets for the Treatment of Hypertensive-Diabetic Nephropathy

• Tipo: Artigo em Revista Científica Internacional
• Data: 2020

Autores

Patinha, D (Autor) Outra; Abreu, C (Autor) Outra; Carvalho, C (Autor) Outra; Cunha, OM (Autor) Outra; Mota, M (Autor) Outra; Afonso, J (Autor) Outra; Sousa, T (Autor) FMUP; Albino Teixeira, A (Autor) Outra; Diniz, C (Autor) FFUP; Morato, M (Autor) FFUP

Revista

Título: Biomedicines

Vol. 8

Páginas: 1-19

Editora: MDPI

Indexação

ISI Web of Knowledge - 8 Citações

Scopus - 10 Citações

Outras Informações

ID Authenticus: P-00T-337

DOI: 10.3390/biomedicines8110529

Abstract (EN): Diabetic nephropathy (DN) and hypertension are prime causes for end-stage renal disease (ESRD) that often coexist in patients, but are seldom studied in combination. Kidney adenosine levels are markedly increased in diabetes, and the expression and function of renal adenosine receptors are altered in experimental diabetes. The aim of this work is to explore the impact of endogenous and exogenous adenosine on the expression/distribution profile of its receptors along the nephron of hypertensive rats with experimentally-induced diabetes. Using spontaneously hypertensive (SHR) rats rendered diabetic with streptozotocin (STZ), we show that treatment of SHR-STZ rats with an agonist of adenosine receptors increases A(2A) immunoreactivity in superficial glomeruli (SG), proximal tubule (PCT), and distal tubule (DCT). Differently, treatment of SHR-STZ rats with a xanthinic antagonist of adenosine receptors decreases adenosine A(3) immunoreactivity in SG, PCT, DCT, and collecting duct. There is no difference in the immunoreactivity against the adenosine A(1) and A(2B) receptors between the experimental groups. The agonist of adenosine receptors ameliorates renal fibrosis, probably via A(2A) receptors, while the antagonist exacerbates it, most likely due to tonic activation of A(3) receptors. The reduction in adenosine A(3) immunoreactivity might be due to receptor downregulation in response to prolonged activation. Altogether, these results suggest an opposite regulation exerted by endogenous and exogenous adenosine upon the expression of its A(2A) and A(3) receptors along the nephron of hypertensive diabetic rats, which has a functional impact and should be taken into account when considering novel therapeutic targets for hypertensive-diabetic nephropathy.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 19