Altememy Dhiya, Kashani Maryam Haji Ghasem, Fateme Amirahmadi, Khosravian Pegah
Department of Pharmaceutics, College of Pharmacy, Al-Zahraa University for Women, Karbala, Iraq.
Department of Cellular and Molecular Biology, School of Biology, Institute of Biological Sciences, Damghan University, Damghan, Iran.
J Adv Pharm Technol Res. 2024 Jul-Sep;15(3):214-219. doi: 10.4103/JAPTR.JAPTR_390_23. Epub 2024 Jul 22.
Rosemary leaf extract, a well-known medicinal plant, can induce neurotrophin gene expression and proliferation in stem cells. Human adipose-derived stem cells (hASCs) with high proliferation and differentiation capacity are easily accessible and can be extracted with the least damage. This study evaluated the effect of rosemary extract (RE) on neurotrophin gene expression at 48 h postinduction in hASCs. hASCs were isolated from healthy female donors, aged 28-35 years, who had undergone abdominal liposuction. Passage-4 stem cells were cultured and treated with different doses of RE (from 30 to 70 µg/ml) containing 40% carnosic acid for 48 h. Reverse transcription-polymerase chain reaction was used to check the expression of neurotrophin genes. The expression of , , and nerve growth factor genes in cells treated with 40-60 µg/ml and the expression of in cells treated with 50-70 µg/ml of RE for 48 h showed a significant increase compared to cells cultured in serum-containing medium. However, different doses of RE showed no effect on brain-derived neurotrophic factor gene expression in the treated cells. RE (50, 60 µg/ml) leads to an increase of neurotrophin gene expression in hASCs as compared to routine cell culture. Hence, this protocol can be used to prepare ideal cell sources for cell therapy.
迷迭香叶提取物是一种著名的药用植物,可诱导干细胞中神经营养因子基因表达和增殖。人脂肪来源干细胞(hASCs)具有高增殖和分化能力,易于获取且提取时损伤最小。本研究评估了迷迭香提取物(RE)对hASCs诱导后48小时神经营养因子基因表达的影响。hASCs从年龄在28 - 35岁、接受腹部抽脂的健康女性供体中分离获得。将第4代干细胞培养并用不同剂量(30至70μg/ml)含40%鼠尾草酸的RE处理48小时。采用逆转录-聚合酶链反应检测神经营养因子基因的表达。与在含血清培养基中培养的细胞相比,用40 - 60μg/ml RE处理48小时的细胞中、和神经生长因子基因的表达以及用50 - 70μg/ml RE处理48小时的细胞中的表达均显著增加。然而,不同剂量的RE对处理后细胞中脑源性神经营养因子基因表达无影响。与常规细胞培养相比,RE(50、60μg/ml)可导致hASCs中神经营养因子基因表达增加。因此,该方案可用于制备用于细胞治疗的理想细胞来源。