Emerging Role of Angiotensin Type 2 Receptor (AT2R)/Akt/NO Pathway in Vascular Smooth Muscle Cell in the Hyperthyroidism

Author(s)

Carrillo-Sepulveda, Maria Alicia ^[1] ; Ceravolo, Graziela S. ^[2] ; Furstenau, Cristina R. ^[1] ; Monteiro, Priscilla de Souza ^[1] ; Bruno-Fortes, Zuleica ^[2] ; Carvalho, Maria Helena ^[2] ; Laurindo, Francisco R. ^[3] ; Tostes, Rita C. ^{[2, 4]} ; Webb, R. Clinton ^[4] ; Barreto-Chaves, Maria Luiza M. ^[1]

Affiliation

^[1] Univ Sao Paulo, Inst Biomed Sci, Dept Anat, Lab Cell Biol & Funct Anat, Sao Paulo - Brazil

^[2] Univ Sao Paulo, Inst Biomed Sci, Lab Hypertens, Sao Paulo - Brazil

^[3] Univ Sao Paulo, Inst Heart, Vasc Biol Lab, Sao Paulo - Brazil

^[4] Georgia Hlth Sci Univ, Dept Physiol, Augusta, GA - USA

• Document type: Journal article
• Source: PLoS One; v. 8, n. 4 APR 24 2013.
• Web of Science Citations: 15

Abstract

Hyperthyroidism is characterized by increased vascular relaxation and decreased vascular contraction and is associated with augmented levels of triiodothyronine (T3) that contribute to the diminished systemic vascular resistance found in this condition. T3 leads to augmented NO production via PI3K/Akt signaling pathway, which in turn causes vascular smooth muscle cell (VSMC) relaxation; however, the underlying mechanisms involved remain largely unknown. Evidence from human and animal studies demonstrates that the renin-angiotensin system (RAS) plays a crucial role in vascular function and also mediates some of cardiovascular effects found during hyperthyroidism. Thus, in this study, we hypothesized that type 2 angiotensin II receptor (AT2R), a key component of RAS vasodilatory actions, mediates T3 induced-decreased vascular contraction. Marked induction of AT2R expression was observed in aortas from T3-induced hyperthyroid rats (Hyper). These vessels showed decreased protein levels of the contractile apparatus: a-actin, calponin and phosphorylated myosin light chain (p-MLC). Vascular reactivity studies showed that denuded aortic rings from Hyper rats exhibited decreased maximal contractile response to angiotensin II (AngII), which was attenuated in aortic rings pre-incubated with an AT2R blocker. Further study showed that cultured VSMC stimulated with T3 (0.1 mu mol/L) for 24 hours had increased AT2R gene and protein expression. Augmented NO levels and decreased p-MLC levels were found in VSMC stimulated with T3, both of which were reversed by a PI3K/Akt inhibitor and AT2R blocker. These findings indicate for the first time that the AT2R/Akt/NO pathway contributes to decreased contractile responses in rat aorta, promoted by T3, and this mechanism is independent from the endothelium. (AU)

• FAPESP's process: 06/61523-7 - Cellular and molecular aspects of muscular plasticity
• Grantee: Anselmo Sigari Moriscot
• Support type: Research Projects - Thematic Grants