Aithal Ashwini P, Bairy Laxminarayana K, Seetharam Raviraja N, Kumar Naveen
Department of Anatomy, Melaka Manipal Medical College (Manipal Campus), Manipal Academy of Higher Education, Manipal, India.
Department of Pharmacology, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, UAE.
3 Biotech. 2021 Feb;11(2):107. doi: 10.1007/s13205-021-02640-y. Epub 2021 Jan 31.
Bone marrow mesenchymal stromal cells (BM-MSCs) are multipotent stem cells which are ideal candidates for use in regenerative medicine. The objectives of this study were to evaluate the hepatoprotective effect of BM-MSC and its combination treatment with silymarin in carbon tetrachloride (CCl)-induced liver cirrhosis animal model and to investigate whether tail vein or portal vein infusion was the ideal route for BM-MSC transplantation. 36 female Wistar rats were randomly divided into six groups ( = 6): Group 1 (normal control), Group 2 (received only CCl, disease model), Group 3 (CCl + BM-MSCs through tail vein), Group 4 (CCl + BM-MSCs through portal vein), Group 5 (CCl + silymarin), Group 6 (CCl + BM-MSCs + silymarin). On the 21st day after treatment, blood samples were collected for biochemical estimations. After the experiment, the rats were sacrificed. Liver was dissected out and processed for histopathology and scanning electron microscopy studies. Liver enzyme and marker analysis, histopathological studies indicated that the combination of BM-MSCs and silymarin was effective in treating liver cirrhosis. Transplanted BM-MSCs in combination with silymarin ameliorated the liver tissue damage through their immunoregulatory activities. Among the two routes, the intravenous administration of cells through the tail vein was found to be more effective and safe.
骨髓间充质基质细胞(BM-MSCs)是多能干细胞,是再生医学中理想的候选细胞。本研究的目的是评估BM-MSC及其与水飞蓟素联合治疗在四氯化碳(CCl)诱导的肝硬化动物模型中的肝保护作用,并研究尾静脉或门静脉注射是否是BM-MSC移植的理想途径。36只雌性Wistar大鼠随机分为六组(每组 = 6只):第1组(正常对照),第2组(仅接受CCl,疾病模型),第3组(CCl + 通过尾静脉注射BM-MSCs),第4组(CCl + 通过门静脉注射BM-MSCs),第5组(CCl + 水飞蓟素),第6组(CCl + BM-MSCs + 水飞蓟素)。治疗后第21天,采集血样进行生化检测。实验结束后,处死大鼠。取出肝脏并进行组织病理学和扫描电子显微镜研究。肝酶和标志物分析、组织病理学研究表明,BM-MSCs与水飞蓟素联合治疗肝硬化有效。移植的BM-MSCs与水飞蓟素联合通过其免疫调节活性改善了肝组织损伤。在两种途径中,发现通过尾静脉静脉注射细胞更有效且更安全。