Open AccessDehydroepiandrosterone‐Mediated Stimulation of Sigma‐1 Receptor Activates Akt‐eNOS Signaling in the Thoracic Aorta of Ovariectomized Rats with Abdominal Aortic Banding
Author(s) -
Bhuiyan Md. Shenuarin,
Tagashira Hideaki,
Fukunaga Kohji
Publication year - 2011
Publication title -
cardiovascular therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 46
eISSN - 1755-5922
pISSN - 1755-5914
DOI - 10.1111/j.1755-5922.2010.00196.x
Subject(s) - enos , medicine , endocrinology , ovariectomized rat , protein kinase b , thoracic aorta , dehydroepiandrosterone , aorta , abdominal aorta , phosphorylation , nitric oxide synthase , nitric oxide , estrogen , biology , androgen , hormone , biochemistry
SUMMARY Objective : Decreased dehydroepiandrosterone (DHEA) levels are associated with endothelial dysfunction and increased cardiovascular mortality in postmenopausal women. Using ovariectomized rats, we first defined whether expression of sigma‐1 receptor (Sig‐1R) in the aorta is regulated following pressure overload (PO) and also after DHEA treatment. We also investigated effects of DHEA known as Sig‐1R agonist on impaired Akt/endothelial nitric oxide synthase (eNOS) signaling in the thoracic aorta under PO. Research design/methods: Wistar rats subjected to bilateral ovariectomy (OVX) were further treated with abdominal aortic stenosis 2 weeks later. DHEA (15 and 30 mg/kg) was administered orally once a day for 14 days starting from 2 weeks after the aortic banding. Results: Time course study indicated that expression of Sig‐1R expression and eNOS decreased time dependently in the thoracic aorta from 1 to 4 weeks after PO. DHEA treatment significantly inhibited the decreased Sig‐1R expression in the thoracic aorta. The DHEA treatment also significantly restored PO‐induced impaired Akt phosphorylation and stimulated eNOS protein expression with concomitant increased Akt‐mediated eNOS phosphorylation (Ser1177). We did not find any changes in the phosphorylation of ERK1/2 and PKCα in the aorta following PO and after treatment with DHEA. Conclusion: We here reported, for the first time, that DHEA treatment induces the upregulation and stimulation of Sig‐1R in the thoracic aorta that stimulate Sig‐1R‐mediated Akt‐eNOS signaling pathways in ovariectomized rats under PO.