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Angiotensin II human acetate

MCE China：Angiotensin II human acetate

Brand：MedChemExpress (MCE)

Cat. No.HY-13948A

CAS：68521-88-0

Synonyms：Angiotensin II acetate; Ang II acetate; DRVYIHPF acetate

Purity：99.62%

Storage：Sealed storage, away from moisture and light, under nitrogen Powder -80°C 2 years -20°C 1 year *In solvent : -80°C, 1 year; -20°C, 6 months (sealed storage, away from moisture and light, under nitrogen)

Shipping：Room temperature in continental US; may vary elsewhere.

Description：Angiotensin II human (Angiotensin II) acetate is a vasoconstrictor and a major bioactive peptide of the renin/angiotensin system. Angiotensin II human acetate plays a central role in regulating human blood pressure, which is mainly mediated by interactions between Angiotensin II and the G-protein-coupled receptors (GPCRs) Angiotensin II type 1 receptor (AT1R) and Angiotensin II type 2 receptor (AT2R). Angiotensin II human acetate stimulates sympathetic nervous stimulation, increases aldosterone biosynthesis and renal actions. Angiotensin II human acetate induces growth of vascular smooth muscle cells, increases collagen type I and III synthesis in fibroblasts, leading to thickening of the vascular wall and myocardium, and fibrosis. Angiotensin II human acetate also induces apoptosis. Angiotensin II human acetate induces capillary formation from endothelial cells via the LOX-1 dependent redox-sensitive pathway.

In Vitro：Most of the known actions of Angiotensin II (Ang II) human acetate are mediated by AT1 receptors, the AT2 receptor contributes to the regulation of blood pressure and renal function[1]. Angiotensin II human acetate raises blood pressure (BP) by a number of actions, the most important ones being vasoconstriction, sympathetic nervous stimulation, increased aldosterone biosynthesis and renal actions. Other Angiotensin II human acetate actions include induction of growth, cell migration, and mitosis of vascular smooth muscle cells, increased synthesis of collagen type I and III in fibroblasts, leading to thickening of the vascular wall and myocardium, and fibrosis. These actions are mediated by type 1 Ang II receptors (AT1)[2]. Angiotensin II (1 nM) induces the expression of LOX-1 and VEGF and enhances capillary formation from human coronary endothelial cells in Matrigel assay. Angiotensin II -mediated expression of LOX-1 and VEGF, capillary formation, intracellular reactive oxygen species generation, and phosphorylation of p38 as well as p44/42 mitogen-activated protein kinases, were suppressed by anti-LOX-1 antibody, nicotinamide-adenine dinucleotide phosphate oxidase inhibitor apocynin and the Ang II type 1 receptor blocker Losartan, but not by the Ang II type 2 receptor blocker PD123319[3].

In Vivo：Angiotensin II human acetate can be used to induce models of hypertension and cardiac hypertrophy[7][8][9]. .f12{ font-size: 12px; } .fwb{ font-weight: bold; } .lh22{ line-height: 22px;; } .lh23 { line-height: 23px; } .pl13{ padding-left: 13px;; } .part { margin-top: 18px; } .mold-first-tit { width: 100%; height: 44px; line-height: 44px; background: #F9F7FB; border-bottom: 1px solid #EBE4F6; padding-left: 16px; box-sizing: border-box; margin-bottom: 17px; } .mold-second-tit:before { content:""; width: 6px; height: 6px; display: inline-block; border-radius: 50%; background: rgba(255,102,0,0.4); margin-right: 12px; position: relative; top: -3px; } .lft-border { border-left: 1px dotted #EBE4F6; padding-right: 12px; margin-left: 3px; box-sizing: border-box; padding-bottom: 12px; } /* .part .dec:last-child { border-bottom: 0; } */ .dec { margin: 10px 15px 0; padding-bottom: 10px; border-bottom: 1px dashed #EBE4F6; } .btm-border { border-left: 1px dashed #EBE4F6; } .text-bg { margin-top: 10px; background: #FFFBF1; padding: 14px; border-bottom: 0; position: relative; } .text-note-bg { margin-top: 10px; background: #FFFDF7; padding: 12px; border-bottom: 0; position: relative; } .text-note { width: 51px; height: 20px; line-height: 20px; background: #FFE2AA; text-align: center; border-radius: 0 0 8px 0; position: absolute; top: 0; left: 0; } .text-note-dec { margin-top: 15px;; } 1. Induction of hypertension[7] Background Angiotensin II human acetate can induce blood vessel constriction: After Ang II binds to its receptor (primarily the AT1 receptor), it activates a series of signaling pathways, such as the opening of calcium channels, leading to an increase in intracellular calcium concentration in vascular smooth muscle cells, causing them to contract, which in turn raises blood pressure;- Promoting inflammatory response: Ang II can also promote the production of inflammatory mediators, for example, by activating NADPH oxidase to produce excessive reactive oxygen species (ROS). These ROS can damage endothelial cells and promote the infiltration of inflammatory cells, resulting in thickening and hardening of the blood vessel walls, further exacerbating the development of hypertension;- Fibrosis and remodeling: Long-term exposure to high levels of Ang II leads to structural changes in the heart and blood vessels, including myocardial hypertrophy, ventricular remodeling, and fibrosis of the blood vessel walls, all of which are important pathological foundations for hypertension and its complications;- Dysregulation of water and sodium metabolism: As mentioned earlier, Ang II stimulates the adrenal cortex to secrete aldosterone, increasing sodium reabsorption in the kidneys, leading to water and sodium retention in the body, increasing blood volume, which raises blood pressure;- Neuroendocrine regulation: Ang II also plays a role in the regulation of the neuroendocrine system, such as influencing the activity of the sympathetic nervous system, enhancing its excitatory effects on the cardiovascular system, indirectly leading to increased blood pressure. Specific Mmodeling Methods Mice: C57/BL6J • male and female • 12-16 wk old • 21-27 gAdministration: 800 ng/kg/min, 0.003 mL/min • 7 days • sc, osmotic pump implanted subcutaneously Note Effect of gender: Chronic ANG II-induced hypertension differs by gender in awake mice. Female mice may be protected from the ANG II-induced increase in blood pressure. Modeling Indicators Key Factor: Blood pressure ↑ on day 7, blood pressure in male was greater than in female. Correlated Product(s): / Opposite Product(s): / .f12{ font-size: 12px; } .fwb{ font-weight: bold; } .lh22{ line-height: 22px;; } .lh23 { line-height: 23px; } .pl13{ padding-left: 13px;; } .part { margin-top: 18px; } .mold-first-tit { width: 100%; height: 44px; line-height: 44px; background: #F9F7FB; border-bottom: 1px solid #EBE4F6; padding-left: 16px; box-sizing: border-box; margin-bottom: 17px; } .mold-second-tit:before { content:""; width: 6px; height: 6px; display: inline-block; border-radius: 50%; background: rgba(255,102,0,0.4); margin-right: 12px; position: relative; top: -3px; } .lft-border { border-left: 1px dotted #EBE4F6; padding-right: 12px; margin-left: 3px; box-sizing: border-box; padding-bottom: 12px; } /* .part .dec:last-child { border-bottom: 0; } */ .dec { margin: 10px 15px 0; padding-bottom: 10px; border-bottom: 1px dashed #EBE4F6; } .btm-border { border-left: 1px dashed #EBE4F6; } .text-bg { margin-top: 10px; background: #FFFBF1; padding: 14px; border-bottom: 0; position: relative; } .text-note-bg { margin-top: 10px; background: #FFFDF7; padding: 12px; border-bottom: 0; position: relative; } .text-note { width: 51px; height: 20px; line-height: 20px; background: #FFE2AA; text-align: center; border-radius: 0 0 8px 0; position: absolute; top: 0; left: 0; } .text-note-dec { margin-top: 15px;; } 2. Induction of Cardiac Hypertrophy[8][9] Background Angiotensin II human acetate activates receptors: Ang II exerts its biological effects primarily by binding to its specific receptor AT1R. Once AT1R is activated, it can trigger various downstream signaling pathways;- Intracellular signaling pathways: The activation of AT1R initiates several intracellular signaling cascades, such as the activation of phospholipase C (PLC), protein kinase C (PKC), and the phosphorylation of members of the mitogen-activated protein kinase (MAPKs) family. These signaling pathways work together to promote the proliferation of cardiac myocytes and protein synthesis, leading to cardiac hypertrophy;- Inflammatory response: Ang II can promote the production of inflammatory factors like tumor necrosis factor α (TNF-α) and interleukin 6 (IL-6), which can further exacerbate myocardial injury and the fibrosis process;- Oxidative stress: Ang II can stimulate the generation of reactive oxygen species (ROS), and excessive ROS can not only directly damage cardiac myocytes but also activate transcription factors like NF-κB, enhancing the inflammatory response and cell apoptosis;- Extracellular matrix remodeling: Prolonged stimulation by Ang II leads to changes in extracellular matrix components, such as excessive deposition of collagen, which increases myocardial stiffness and disrupts normal heart function. Specific Mmodeling Methods Mice: C57/BL6J • male • 8 wk old &bullAdministration: 2 μg/kg/min • 4 weeks • sc, osmotic pump implanted subcutaneously Note Modeling Indicators Indicator changes: Blood pressure in WT mice increased significantly.Appearance monitoring: cardiac hypertrophy and fibrosis. Correlated Product(s): / Opposite Product(s): Eplerenone (HY-B0251)

IC50 & Target：AT2 Receptor AT1 Receptor

Sequence：Asp-Arg-Val-Tyr-Ile-His-Pro-Phe

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References：

[1]. de Gasparo M, et al. International union of pharmacology. XXIII. The angiotensin II receptors. Pharmacol Rev. 2000 Sep;52(3):415-72.  [Content Brief]

[2]. Fyhrquist F, et al. Role of angiotensin II in blood pressure regulation and in the pathophysiology of cardiovascular disorders. J Hum Hypertens. 1995 Nov;9 Suppl 5:S19-24.  [Content Brief]

[3]. Hu C, et al. Angiotensin II induces capillary formation from endothelial cells via the LOX-1 dependent redox-sensitive pathway. Hypertension. 2007;50(5):952-957.  [Content Brief]

[4]. Nabah YN, et al. Angiotensin II induces neutrophil accumulation in vivo through generation and release of CXC chemokines. Circulation. 2004;110(23):3581-3586.  [Content Brief]

[5]. Crowley SD, et al. Angiotensin II causes hypertension and cardiac hypertrophy through its receptors in the kidney. Proc Natl Acad Sci U S A. 2006 Nov 21;103(47):17985-90.  [Content Brief]