PMID- 33010349 OWN - NLM STAT- MEDLINE DCOM- 20211026 LR - 20211026 IS - 1873-2747 (Electronic) IS - 0361-9230 (Linking) VI - 165 DP - 2020 Dec TI - Mesenchymal stem cells-derived mitochondria transplantation mitigates I/R-induced injury, abolishes I/R-induced apoptosis, and restores motor function in acute ischemia stroke rat model. PG - 70-80 LID - S0361-9230(20)30640-7 [pii] LID - 10.1016/j.brainresbull.2020.09.018 [doi] AB - Acute ischemia stroke (AIS) is one of the leading causes of mortality and disability worldwide, and its neurological impacts are devastating and permanent. There is no efficient and real treatment for acute ischemia stroke so far. Therefore, development of efficient therapeutic strategies is under focus of investigations by basic and clinical scientists. Brain is one of the organs with high energy consumption and metabolism. Hence, its functionality is highly dependent on mitochondrial activity and integrity. Therefore, mitochondria play a vital homeostatic role in neurons physiology and mitochondrial dysfunction implications have been reported in a variety of nervous system diseases including acute ischemia stroke. In an attempt to investigate and introduce a novel potential therapeutic strategy for AIS, we isolated healthy mitochondria from human umbilical cord derived mesenchymal stem cells (hUC-MSCs) followed by their intracerebroventricular transplantation in a rat model of ischemia, i.e. middle cerebral artery occlusion (MCAO). Here we report that the mitochondrial transplantation ameliorated the reperfusion/ischemia-induced damages as reflected by declined blood creatine phosphokinase level, abolished apoptosis, decreased astroglyosis and microglia activation, reduced infarct size, and improved motor function. Although further preclinical and clinical studies are required, our findings strongly suggest that transplantation of MSCs-derived mitochondria is a suitable, potential and efficient therapeutic option for acute ischemia stroke. CI - Copyright (c) 2020 Elsevier Inc. All rights reserved. FAU - Pourmohammadi-Bejarpasi, Zahra AU - Pourmohammadi-Bejarpasi Z AD - Medical Biotechnology Department, Paramedicine Faculty, Guilan University of Medical Sciences, Rasht, Iran. FAU - Roushandeh, Amaneh Mohammadi AU - Roushandeh AM AD - Medical Biotechnology Department, Paramedicine Faculty, Guilan University of Medical Sciences, Rasht, Iran; Anatomical Sciences Department, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran. Electronic address: mohammadi_roushandeh@gums.ac.ir. FAU - Saberi, Alia AU - Saberi A AD - Neuroscience Research Center, Guilan University of Medical Sciences, Rasht, Iran. FAU - Rostami, Mojdeh Kheirandish AU - Rostami MK AD - Medical Biotechnology Department, Paramedicine Faculty, Guilan University of Medical Sciences, Rasht, Iran. FAU - Toosi, Seyyed Mohammadtaghi Razavi AU - Toosi SMR AD - Medical Biotechnology Department, Paramedicine Faculty, Guilan University of Medical Sciences, Rasht, Iran. FAU - Jahanian-Najafabadi, Ali AU - Jahanian-Najafabadi A AD - Department of Pharmaceutical Biotechnology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran. FAU - Tomita, Kazuo AU - Tomita K AD - Department of Applied Pharmacology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan. FAU - Kuwahara, Yoshikazu AU - Kuwahara Y AD - Division of Radiation Biology and Medicine, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan. FAU - Sato, Tomoaki AU - Sato T AD - Department of Applied Pharmacology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan. FAU - Roudkenar, Mehryar Habibi AU - Roudkenar MH AD - Medical Biotechnology Department, Paramedicine Faculty, Guilan University of Medical Sciences, Rasht, Iran; Neuroscience Research Center, Guilan University of Medical Sciences, Rasht, Iran. Electronic address: roudkenar@gums.ac.ir. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20201001 PL - United States TA - Brain Res Bull JT - Brain research bulletin JID - 7605818 SB - IM MH - Animals MH - Apoptosis/*physiology MH - Brain/metabolism MH - Disease Models, Animal MH - Ischemic Stroke/*metabolism MH - *Mesenchymal Stem Cell Transplantation MH - Mitochondria/metabolism MH - Motor Skills/*physiology MH - Neurons/metabolism MH - Rats MH - Reperfusion Injury/metabolism/*therapy OTO - NOTNLM OT - Apoptosis OT - Brain stroke OT - Mesenchymal stems cells OT - Mitochondrial transplantation EDAT- 2020/10/04 06:00 MHDA- 2021/10/27 06:00 CRDT- 2020/10/03 20:08 PHST- 2020/06/06 00:00 [received] PHST- 2020/08/24 00:00 [revised] PHST- 2020/09/23 00:00 [accepted] PHST- 2020/10/04 06:00 [pubmed] PHST- 2021/10/27 06:00 [medline] PHST- 2020/10/03 20:08 [entrez] AID - S0361-9230(20)30640-7 [pii] AID - 10.1016/j.brainresbull.2020.09.018 [doi] PST - ppublish SO - Brain Res Bull. 2020 Dec;165:70-80. doi: 10.1016/j.brainresbull.2020.09.018. Epub 2020 Oct 1.