i-Inositol是一种参与胰岛素信号转导、细胞骨架转导等一系列生物过程的糖醇。
Cas No.:87-89-8
Sample solution is provided at 25 µL, 10mM.
i-Inositol is a sugar alcohol involved in a series of biological processes such as insulin signal transduction and cytoskeleton transduction. i-Inositol is mainly present in glial cells and plays an osmotic role. i-Inositol can be used in research related to polycystic ovary syndrome, sperm function, and diabetes improvement[1-4].
In vitro, i-Inositol (100nM–10mM) was co-treated with PMA (1–100ng/ml), LPS (0.1–10μg/ml), IFN-γ (150unit/ml), or CsA (0.5–50nM) in RAW 264.7 mouse macrophages for 24 hours. i-Inositol restored taurine transport activity in a dose-dependent manner[5]. i-Inositol (0.02–0.10mg/ml) was used to treat DU-145 prostate cancer cells for 72 hours. i-Inositol significantly reduced cell viability[6].
In vivo, i-Inositol (360mg/kg/day) was orally administered daily to C57 BL/6J mice for 14 days. i-Inositol significantly reduced cadmium-induced serum urea nitrogen and creatinine levels, increased renal glutathione content and glutathione peroxidase activity, decreased tumor necrosis factor-α and inducible nitric oxide synthase expression, reduced monocyte chemoattractant protein-1, kidney injury molecule-1, and inositol oxygenase immunoreactivity, decreased the number of apoptotic cells, and protected kidney morphology[7]. i-Inositol (1.2mg/g/day) was intraperitoneally injected daily into female CD-1 Swiss mice for 15 days. i-Inositol significantly reduced white adipose tissue accumulation and improved insulin sensitivity in the mice[8].
References:
[1] Merviel P, James P, Bouée S, et al. Impact of myo-inositol treatment in women with polycystic ovary syndrome in assisted reproductive technologies. Reprod Health. 2021 Jan 19;18(1):13.
[2] Bizzarri M, Monti N, Piombarolo A, et al. Myo-Inositol and D-Chiro-Inositol as Modulators of Ovary Steroidogenesis: A Narrative Review. Nutrients. 2023 Apr 13;15(8):1875.
[3] Benvenga S, Marini HR, Micali A, et al. Protective Effects of Myo-Inositol and Selenium on Cadmium-Induced Thyroid Toxicity in Mice. Nutrients. 2020 Apr 26;12(5):1222.
[4] Long L, Huang Q, Song T, Dai Z. Myo-inositol rescued insulin resistance and dyslipidemia in db/db mice. J Appl Biomed. 2024 Jun;22(2):74-80.
[5] Kim HW, Kim JH, An HS, et al. Myo-inositol restores the inflammation-induced down-regulation of taurine transport by the murine macrophage cell line, RAW 264.7. Life Sci. 2003 Sep 26;73(19):2477-89.
[6] Islam MJ, Muntaha S, Masum MM, et al. Proteomic Analysis of Anticancer Effect of Myo-inositol in Human Prostate Cancer (DU-145) Cell Line. Asian Pac J Cancer Prev. 2024 Dec 1;25(12):4447-4455.
[7] Pallio G, Micali A, Benvenga S, et al. Myo-inositol in the protection from cadmium-induced toxicity in mice kidney: An emerging nutraceutical challenge. Food Chem Toxicol. 2019 Oct;132:110675.
[8] Croze ML, Vella RE, Pillon NJ, et al. Chronic treatment with myo-inositol reduces white adipose tissue accretion and improves insulin sensitivity in female mice. J Nutr Biochem. 2013 Feb;24(2):457-66.
i-Inositol是一种参与胰岛素信号转导、细胞骨架转导等一系列生物过程的糖醇。i-Inositol主要存在于神经胶质细胞中起渗透作用。i-Inositol可用于多囊卵巢综合征、精子功能、糖尿病改善的相关研究[1-4]。
在体外,i-Inositol(100nM–10mM)与PMA(1–100ng/ml)、LPS(0.1–10μg/ml)、IFN-γ(150unit/ml)或CsA(0.5–50nM)共同处理RAW 264.7小鼠巨噬细胞24小时。i-Inositol以剂量依赖的方式恢复牛磺酸转运活性[5]。i-Inositol(0.02–0.10mg/ml)处理DU-145前列腺癌细胞72小时。i-Inositol显著降低细胞活力[6]。
在体内,i-Inositol(360mg/kg/day)每日口服,用于处理C57 BL/6J小鼠14天。i-Inositol显著降低了镉诱导的血清尿素氮和肌酐水平,增加了肾脏谷胱甘肽含量和谷胱甘肽过氧化物酶活性,降低了肿瘤坏死因子-α和诱导型一氧化氮合酶表达,减少了单核细胞趋化蛋白-1、肾损伤分子-1和肌醇加氧酶免疫反应性,减少了凋亡细胞数量,并保护了肾脏形态[7]。i-Inositol(1.2mg/g/day)每日腹腔注射,用于处理雌性CD-1 Swiss小鼠15天。i-Inositol显著减少了小鼠的白色脂肪组织积累并改善了胰岛素敏感性[8]。
| Cell experiment [1]: | |
Cell lines | DU-145 prostate cancer cells (human prostate adenocarcinoma cell line) |
Preparation Method | DU-145 cells were maintained in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS), 1% sodium pyruvate, and 1% penicillin-streptomycin at 37°C in a humidified incubator with 5% CO₂. The cells were treated with i-Inositol at concentrations ranging from 0.02 to 0.10mg/ml for 72 hours. |
Reaction Conditions | 0.02–0.10mg/ml; 72h |
Applications | i-Inositol significantly reduced DU-145 cell viability in a dose-dependent manner. Proteomic analysis revealed marked differences in protein expression between treated and untreated cells, with suppression of proteins like Annexin A2 and Cofilin-1-A in controls, and upregulation of proteins such as Rho GTPase-activating protein, Apoptotic protease-activating factor 1 (APAF1), and TNF receptor-associated factor 2 (TRAF2) in treated samples, indicating modulation of key signaling pathways involved in tumor suppression and oncogenesis. |
| Animal experiment [2]: | |
Animal models | Female CD-1 Swiss mice |
Preparation Method | Mice were given daily intraperitoneal injection of i-Inositol (1.2mg/g/day) for 15 days. |
Dosage form | 1.2mg/g/day; i.p.; 15 consecutive days |
Applications | i-Inositol treatment significantly reduced white adipose tissue accretion, decreased adipocyte volume, improved glucose tolerance, enhanced insulin sensitivity, increased insulin-induced PKB/Akt phosphorylation in skeletal muscle, reduced plasma non-esterified fatty acids, and increased total plasma antioxidant activity. |
References: | |
| Cas No. | 87-89-8 | SDF | |
| 别名 | 肌醇; myo-Inositol; meso-Inositol | ||
| 化学名 | cyclohexane-1,2,3,4,5,6-hexaol | ||
| Canonical SMILES | OC1C(O)C(O)C(O)C(O)C1O | ||
| 分子式 | C6H12O6 | 分子量 | 180.16 |
| 溶解度 | 9mg/ml in DMSO;≥ 50mg/mL in Water | 储存条件 | Store at -20°C |
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1 mg | 5 mg | 10 mg |
| 1 mM | 5.5506 mL | 27.7531 mL | 55.5062 mL |
| 5 mM | 1.1101 mL | 5.5506 mL | 11.1012 mL |
| 10 mM | 555.1 μL | 2.7753 mL | 5.5506 mL |
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2.
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