インデックス付き
  • Jゲートを開く
  • Genamics JournalSeek
  • アカデミックキー
  • ジャーナル目次
  • 研究聖書
  • 中国国家知識基盤 (CNKI)
  • シマゴ
  • ウルリッヒの定期刊行物ディレクトリ
  • 電子ジャーナルライブラリ
  • レフシーク
  • ハムダード大学
  • エブスコ アリゾナ州
  • OCLC-WorldCat
  • SWBオンラインカタログ
  • 仮想生物学図書館 (vifabio)
  • パブロン
  • ミアル
  • 科学インデックスサービス (SIS)
  • ユーロパブ
  • Google スカラー
このページをシェアする
ジャーナルチラシ
Flyer image

概要

Mas Receptor Responsive to Different Pathophysiological Nanotechnology by Stimuli-A Systematic Review

Silva James

The Mas proto-oncogene encodes a G protein-coupled receptor that has been portrayed as a utilitarian receptor for the cardio protective part of the renin-angiotensin framework (RAS), Angiotensin (Ang)-(1-7). The point of this current ponder was to assess the responsiveness of Mas expression in hearts amid distinctive physiological and obsessive conditions in rats. Physical preparing was considered a physiological condition, whereas isoproterenol-induced hypertrophy, myocardial localized necrosis and DOCA-salt demonstrate of hypertension were utilized as neurotic models of heart harm. The expression of Mas was analyzed by western smudging. In spite of the fact that swim-trained rats displayed noteworthy cardiac hypertrophy, our physical preparing convention was unable to initiate changes within the expression of Mas. Myocardial localized necrosis too essentially diminished the expression of Mas after 21 days of myocardial ischemia. Furthermore, Mas expression levels were expanded in hearts of DOCA-salt rats. Our display information show that Mas expression is responsive to diverse neurotic boosts, subsequently proposing that Mas receptor is included within the homeostasis of the heart, as well as within the foundation and movement of cardiac maladies.

免責事項: この要約は人工知能ツールを使用して翻訳されており、まだレビューまたは確認されていません