地塞米松磷酸二鈉作用機(jī)制 - Medchemexpress - MCE中國(guó)

1、Product Data SheetDexamethasone phosphate disodiumCat. No.: HY-B1829ACAS No.: 2392-39-4分式: CHFNaOP分量: 516.4作靶點(diǎn): Glucocorticoid Receptor作通路: GPCR/G Protein儲(chǔ)存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性數(shù)據(jù)體外實(shí)驗(yàn) H2O : 100 mg/mL (193.65 mM)DMSO : 1 mg/mL (1.94 mM; ultrasonic and

2、 warming and heat to 80C)* means soluble, but saturation unknown.SolventMass1 mg 5 mg 10 mgConcentration制備儲(chǔ)備液1 mM 1.9365 mL 9.6824 mL 19.3648 mL5 mM 0.3873 mL 1.9365 mL 3.8730 mL10 mM 0.1936 mL 0.9682 mL 1.9365 mL請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液；旦配成溶液，請(qǐng)分裝保存，避免反復(fù)凍融造成的產(chǎn)品失效。儲(chǔ)備液的保存式和期限：-80C, 6 months; -20C,

3、1 month。-80C 儲(chǔ)存時(shí)，請(qǐng)?jiān)?6 個(gè)內(nèi)使，-20C 儲(chǔ)存時(shí)，請(qǐng)?jiān)?1 個(gè)內(nèi)使。BIOLOGICAL ACTIVITY物活性 Dexamethasone phosphate disodium is a glucocorticoid receptor agonist.IC & Target Glucocorticoid receptor1體外研究Dexamethasone regulates several transcription factors, including activator protein-1, nuclear factor-AT, and nuclearfactor-

4、kB, leading to the activation and repression of key genes involved in the inflammatory response1.Dexamethasone potently inhibits granulocyte-macrophage colony stimulating factor (GM-CSF) release from A549cells with EC50 of 2.2 nM. Dexamethasone (EC50=36 nM) induces transcription of the 2-receptor is

5、 found to correlatewith glucocorticoid receptor (GR) DNA binding and occurred at 10-100 fold higher concentrations than the inhibitionof GM-CSF release. Dexamethasone (IC50=0.5 nM) inhibits a 3B (NF-B, IB, and I-B), which is associated withPage 1 of 2 www.MedChemEinhibition of GM-CSF release2.體內(nèi)研究 T

6、reatment with Dexamethasone at a dose of 25 mg/kg efficiently inhibits lipopolysaccharide (LPS)-inducedinflammation. In our experimental system, treatment with a single dose of Dexamethasone 10 mg/kg (i.p.)significantly decreases recruitment of granulocytes as well as spontaneous production of oxyge

7、n radicals comparedwith animals expose to LPS and injected with solvent alone (saline). The effects are statistically significant whenadministered both 1 h before and 1 h after inhalation of LPS. The number of granulocytes in BALF decreased to levelscomparable to healthy animals (given an aerosol of

8、 water)3. Rats treated with Dexamethasone consume less foodand weighed less than control rats. Treated rats also weigh less than pair-fed animals though their food intake issimilar. Five days of Dexamethasone injection result in a significant increase in both the liver mass (+42%) and theliver to bo

9、dy weight ratio (+65%). The wet weight of gastrocnemius muscle decreases 20% after 5 days of treatment,but it remains unaffected relative to body weight (g/100 g body weight), indicating that muscle weight loss paralleledbody weight loss4.PROTOCOLAnimal Rats: Male Sprague-Dawley rats are used. Dexam

10、ethasone-treated rats are injected intraperitoneally once daily withAdministration 34 Dexamethasone (1.5 mg/kg body weight) for 5 days and are allowed to feed ad libitum. Control rats receive notreatment and are fed ad libitum. In order to take into account the decrease in food intake induced byDexa

11、methasone treatment, a third group of pair-fed rats are used. These rats are provided with the same amount offood as Dexamethasone-injected rats and are treated with a daily isovolumic intraperitoneal injection of NaCl (0.9%)for 5 days. After the final injection of Dexamethasone or NaCl, the animals

12、 are fasted overnight prior to being killedby decapitation4.Mice: Female C57Bl/6JBom mice (age 10-12 weeks) are used in all experiments. Dexamethasone is administered as asingle injection of 1 or 10 mg/kg. Dexamethasone is dissolved in saline and 400 L are injected intraperitoneally,either 1 h befor

13、e or 1 h after LPS exposure. In one experiment, N-acetylcysteine (NAC) (100 and 500 mg/kg) isinjected successively every 4-5 h, starting 1 h before challenge (five injections in total). A control group of LPS-exposed animals are injected intraperitoneally with solvent alone (saline). Intratracheal a

14、dministration is performedby instillation of 100 L NAC (50, 100 or 500 mg/kg) or Dexamethasone (10 mg/kg) into the lungs of miceanaesthetized with 15 mg/kg Rapinovet (i.v.)3.MCE has not independently confirmed the accuracy of these methods. They are for reference only.REFERENCES1. LaLone CA, et al.

15、Effects of a glucocorticoid receptor agonist, Dexamethasone, on fathead minnow reproduction, growth, and development. EnvironToxicol Chem. 2012 Mar;31(3):611-22.2. Adcock IM, et al. Ligand-induced differentiation of glucocorticoid receptor (GR) trans-repression and transactivation: preferential targ

16、etting of NF-kappaB and lack of I-kappaB involvement. Br J Pharmacol. 1999 Jun;127(4):1003-11.3. Rocksn D, et al. Differential anti-inflammatory and anti-oxidative effects of Dexamethasone and N-acetylcysteine in endotoxin-induced lunginflammation. Clin Exp Immunol. 2000 Nov;122(2):249-56.4. Roussel D, et al. Dexamethasone treatment specifically increases the basal proton conductance of rat liver mitochondria. FEBS Lett. 2003 Apr 24;541(1-3):75