المراجع (Citations)
1 publicationsمنشورات الباحثين الذين استخدموا هذا المنتجالوصف (Description)
Entacapone is a potent, reversible, peripherally acting and orally active inhibitor of catechol-O-methyltransferase (COMT), which effectively inhibits rat liver total COMT with IC50 and Ki values of 20.1nM and 10.7nM, respectively[1]. Entacapone has IC50 values of 14.3nM and 73.3nM for rat liver soluble COMT (S-COMT) and rat liver membrane-bound COMT (MB-COMT), respectively[1]. Entacapone is a weak uncoupler of oxidative phosphorylation[2]. Entacapone is commonly used in combination with levodopa (L-DOPA) to treat Parkinson's disease[3]. Entacapone is a ferroptosis inhibitor that can enhance antioxidant capacity[4].
In vitro, treatment of esophageal cancer cell lines (KYSE-30 and YM-1 cells) with Entacapone (25-150μM) for 48h reduced cell viability in a dose-dependent manner, and induced apoptosis and altered the cell cycle at a concentration of 140μM[5]. Treatment of Hep-G2 cells with Entacapone (50μM) for 48h increased the amount of m6A on mRNA in cells[6].
In vivo, oral treatment of C57BL/6J mice with Entacapone (10, 50, 200mg/kg/day) for 21 days significantly improved ANA-12-induced memory impairment and the reduction of hippocampal brain-derived neurotrophic factor (BDNF) and tyrosine kinase receptor B (TrkB) expression, and significantly increased the number of Ki67-positive proliferating cells, doublecortin-positive immature neurons, and phosphorylated cAMP response element binding protein (pCREB)-positive cells in the dentate gyrus of the hippocampus[7]. Oral treatment of C57BL/6J mice with Entacapone (50mg/kg) for 21 days induced changes in the expression of proteins involved in synaptic transmission, cellular processes, cell signaling, cytoskeletal structure regulation, energy metabolism, and various other cellular responses in the mouse hippocampus[8].
References:
[1] Forsberg M, Lehtonen M, Heikkinen M, et al. Pharmacokinetics and pharmacodynamics of entacapone and tolcapone after acute and repeated administration: a comparative study in the rat[J]. Journal of Pharmacology and Experimental Therapeutics, 2003, 304(2): 498-506.
[2] Nissinen E, Kaheinen P, Penttilä K E, et al. Entacapone, a novel catechol-O-methyltransferase inhibitor for Parkinson's disease, does not impair mitochondrial energy production[J]. European journal of pharmacology, 1997, 340(2-3): 287-294.
[3] Stocchi F, Rascol O, Kieburtz K, et al. Initiating levodopa/carbidopa therapy with and without entacapone in early Parkinson disease: the STRIDE‐PD study[J]. Annals of neurology, 2010, 68(1): 18-27.
[4] Yang J, Sun X, Huang N, et al. Entacapone alleviates acute kidney injury by inhibiting ferroptosis[J]. The FASEB Journal, 2022, 36(7): e22399.
[5] Ramedani F, Jafari S M, Saghaeian Jazi M, et al. Anti‐cancer effect of entacaponeon esophageal cancer cells via apoptosis induction and cell cycle modulation[J]. Cancer Reports, 2023, 6(3): e1759.
[6] Peng S, Xiao W, Ju D, et al. Identification of entacapone as a chemical inhibitor of FTO mediating metabolic regulation through FOXO1[J]. Science Translational Medicine, 2019, 11(488): eaau7116.
[7] Yoo D Y, Jung H Y, Kim W, et al. Entacapone promotes hippocampal neurogenesis in mice[J]. Neural Regeneration Research, 2021, 16(6): 1005-1010.
[8] Yoo D Y, Jung H Y, Kim W, et al. Entacapone treatment modulates hippocampal proteins related to synaptic vehicle trafficking[J]. Cells, 2020, 9(12): 2712.
البروتوكول (Protocol)
| Cell experiment [1]: | |
Cell lines | KYSE-30 and YM-1 of esophageal squamous cancer cell (ESCC) lines |
Preparation Method | Cells were seeded into 96-well plates at a density of 104 cells/well, the culture medium was removed and then cells were treated with different concentrations (25, 50, 75, 100, 125, and 150μM) of Entacapone with a final volume of 200μl. As vehicle control cells were treated with DMSO (0.3%) with same condition. After 48h treatment, cell viability was measured using the MTT assay. |
Reaction Conditions | 25-150μM; 48h |
Applications | Entacapone was cytotoxic to both esophageal cancer cell lines in a dose-dependent manner. |
| Animal experiment [2]: | |
Animal models | C57BL/6J mice |
Preparation Method | Mice (n=10 per group) were randomly divided into four groups: the vehicle-treated control group and the groups treated with 10, 50, or 200mg/kg Entacapone. Vehicle or Entacapone was orally administered to the mice once a day using a feeding needle and ANA-12 was injected into the hippocampus at a rate of 0.5μL/min for 5min. Administered Entacapone for 21 days. Immunohistochemical staining was used to analyze the number of Ki67-positive proliferating cells, doublecortin-positive immature neurons and phosphorylated cAMP response element binding protein (pCREB)-positive cells in the dentate gyrus of the hippocampus of mice. |
Dosage form | 10, 50, 200mg/kg/day for 21 days; p.o. |
Applications | After Entacapone treatment, the numbers of Ki67-positive proliferating cells, doublecortin-positive immature neurons, and phosphorylated cAMP response element-binding protein (pCREB)-positive cells were significantly increased. |
References: [1]Ramedani F, Jafari S M, Saghaeian Jazi M, et al. Anti‐cancer effect of entacaponeon esophageal cancer cells via apoptosis induction and cell cycle modulation[J]. Cancer Reports, 2023, 6(3): e1759. [2]Yoo D Y, Jung H Y, Kim W, et al. Entacapone promotes hippocampal neurogenesis in mice[J]. Neural Regeneration Research, 2021, 16(6): 1005-1010. | |
وثائق المنتج (Product Documents)
الخصائص الكيميائية (Chemical Properties)
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية
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