Combination of Sleeve Gastrectomy and Mesenchymal Stem Cells Improves Insulin Resistance by Modulating Pro-inflammatory Milieu in Obese Type 2 Diabetic Rat Model
Putra A., Alif I., Makarim F.R., Ekasaputra V.M., Mughni A., Prasetya A., Nugrahadi D.E., Putranto I., Riwanto I.
Abstract
BACKGROUND: Obesity is a major risk factor for the onset of insulin resistance (IR) and type 2 diabetes mellitus (T2DM) caused by chronic inflammation of the islets of Langerhans. Sleeve gastrectomy (SG) procedure increases particular hormone which stimulates insulin sensitivity. Mesenchymal stem cells (MSCs) can also exhibit potential immunomodulatory properties through their paracrine effects; however, the mechanism regarding combination of them could not be adequately explained. AIM: In this study, we explore the potential of SG followed by injection of MSCs in type 2 diabetic rats with obesity in improving IR. MATERIALS AND METHODS: This study used a pre and post control group design with 18 rats that divided into three groups: Control (C), SG, and SG + MSCs (SG+M). On day 10, the level of interleukin (IL-6), IL-10, and homeostasis model assessment of IR (HOMA-IR) was evaluated using ELISA. RESULTS: This study showed a significant decrease of IL-6 level in all treatment groups on day 10, in which SG + M group showed optimum inhibition. This result was in line with the optimum increase of IL-10 in SG + M group. Moreover, our study also revealed the optimum decrease of HOMA-IR in SG + M group on day 10. CONCLUSION: Combination of SG and MSCs can optimally improve IR by modulating pro-inflammatory milieu though inhibiting IL-6 level and upregulating IL-10 level in obese T2DM rat model.
The promise(s) of mesenchymal stem cell therapy in averting preclinical diabetes: lessons from in vivo and in vitro model systems
Kotikalapudi N., Mungamuri S.K., Nemani H., Ramesh R B., Ramesh R B., Sampath S.J.P., Sukesh Narayan S., Venkatesan V.
Mechanisms Linking Inflammation to Insulin Resistance
Chen L., Chen L., Chen R., Liang F., Liang F., Wang H., Wang H.
Regulation of insulin sensitivity by serine/threonine phosphorylation of insulin receptor substrate proteins IRS1 and IRS2
Copps K.D., White M.F.
Activation of STAT3 by IL-6 and IL-10 in primary human macrophages is differentially modulated by suppressor of cytokine signaling 3
Fischer P., Haan S., Heinrich P.C., Muller-Newen G., Niemand C., Nimmesgern A., Rossaint R., Schaper F.
In vitro regulation of il-6 and tgf-ß by mesenchymal stem cells in systemic lupus erythematosus patients
Alif I., Darlan D.M., Ikhsan R., Jusuf N.K., Munir D., Putra A., Alif I., Darlan D.M., Ikhsan R., Jusuf N.K., Munir D., Putra A., Alif I., Darlan D.M., Ikhsan R., Jusuf N.K., Munir D., Putra A., Alif I., Darlan D.M., Ikhsan R., Jusuf N.K., Munir D., Putra A., Alif I., Darlan D.M., Ikhsan R., Jusuf N.K., Munir D., Putra A., Alif I., Darlan D.M., Ikhsan R., Jusuf N.K., Munir D., Putra A.
Ghrelin - Physiological functions and regulation
Abdalla M.M.I.
Therapeutic Effects of Adipose Stem Cells from Diabetic Mice for the Treatment of Type 2 Diabetes
Dong X., Song L., Strange C., Wang H., Wang M.
Mesenchymal stem cells under hypoxia condition inhibit peritoneal adhesion by suppressing the prolonged release of interleukin-6
Darlan D.M., Ekasaputra V.M., Muhar A.M., Nasution I.P.A., Paramita D.A., Putra A.
Hypoxia-mesenchymal stem cells inhibit intra-peritoneal adhesions formation by upregulation of the il-10 expression
Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M., Muhar A.M., Munir D., Putra A., Warli S.M.
Contribution of adipose tissue inflammation to the development of type 2 diabetes mellitus
Burhans M.S., Burhans M.S., Hagman D.K., Kratz M., Kratz M., Kuzma J.N., Schmidt K.A., Schmidt K.A.
