Mitochondrial Transplantation Therapy for Ischemic Stroke: Progress and Challenges

Ischemic stroke is characterized by high morbidity, high disability, high mortality, high recurrence and high economic burden, which remains second leading cause of death and the third leading cause of disability worldwide. Although continuous progress has been made in vascular recanalization therapy and pharmacological treatment, the effect of these treatments for ischemic stroke has not yet met the expectations of patients and their families. Current clinical therapeutic regimens focus primarily on revascularization and antithrombotic, while neuroprotective strategies are still notably lacking. The main purpose of acute ischemic stroke treatment is to rescue neurons in ischemic penumbra, but high-energy-consuming neurons are highly sensitive and vulnerable to ischemia-hypoxia due to cessation of cerebral blood flow. Mitochondria damage and dysfunction is one of the most critical pathological consequences of hypoxia, as well as a significant contributor to neuronal death. Emerging evidence have demonstrated that mitochondria-targeted strategy is promising for treatment of ischemic stroke, and drugs such as butylphthalide and edaravone have been demonstrated to restore mitochondrial function. However, sustained ischemic-hypoxia often leads to irreversible mitochondrial damage in acute phase of cerebral ischemia. Therefore, mitochondrial transplantation or replacement might be an alternative and effective strategy for treatment of ischemic stroke, especially in acute phase. Although evidence from animal studies have shown that mitochondrial transplantation could improve energy metabolism and prevent cell death, clinical studies have not demonstrated its therapeutic efficacy in practice, highlighting the need for in-depth investigation into mitochondrial transplantation. This article reviews the advances and limitations in therapeutic role and mechanisms of mitochondrial transplantation therapy for ischemic stroke, and discusses the challenges in its translational and clinical application. Mitochondrial transplantation therapy for ischemic stroke. The source of mitochondria, methods for enhancing effectiveness of mitochondrial delivery and transplantation, and the potential mechanism of mitochondrial transplantation therapy for ischemic stroke

Authors

Institutions

Publication Details

Journal
Cellular and Molecular Neurobiology
Published
2026-02-06
DOI
https://doi.org/10.1007/s10571-026-01682-1
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mitochondrial Transplantation Therapy for Ischemic Stroke: Progress and Challenges

Meijuan Dang, Ziwei Lu, Gui-Lian Zhang, Hong Fan et al.
Cellular and Molecular Neurobiology
Mitochondrial Function and Pathology
article

Mitochondrial Transplantation Therapy for Ischemic Stroke: Progress and Challenges

Meijuan Dang, Ziwei Lu, Gui-Lian Zhang, Hong Fan, Ye Li, Kun Chen, Li-Li Zhao, Xue-Ling Yang, Tao Li, Zhi-Hong Zhao
article en

Abstract

Ischemic stroke is characterized by high morbidity, high disability, high mortality, high recurrence and high economic burden, which remains second leading cause of death and the third leading cause of disability worldwide. Although continuous progress has been made in vascular recanalization therapy and pharmacological treatment, the effect of these treatments for ischemic stroke has not yet met the expectations of patients and their families. Current clinical therapeutic regimens focus primarily on revascularization and antithrombotic, while neuroprotective strategies are still notably lacking. The main purpose of acute ischemic stroke treatment is to rescue neurons in ischemic penumbra, but high-energy-consuming neurons are highly sensitive and vulnerable to ischemia-hypoxia due to cessation of cerebral blood flow. Mitochondria damage and dysfunction is one of the most critical pathological consequences of hypoxia, as well as a significant contributor to neuronal death. Emerging evidence have demonstrated that mitochondria-targeted strategy is promising for treatment of ischemic stroke, and drugs such as butylphthalide and edaravone have been demonstrated to restore mitochondrial function. However, sustained ischemic-hypoxia often leads to irreversible mitochondrial damage in acute phase of cerebral ischemia. Therefore, mitochondrial transplantation or replacement might be an alternative and effective strategy for treatment of ischemic stroke, especially in acute phase. Although evidence from animal studies have shown that mitochondrial transplantation could improve energy metabolism and prevent cell death, clinical studies have not demonstrated its therapeutic efficacy in practice, highlighting the need for in-depth investigation into mitochondrial transplantation. This article reviews the advances and limitations in therapeutic role and mechanisms of mitochondrial transplantation therapy for ischemic stroke, and discusses the challenges in its translational and clinical application. Mitochondrial transplantation therapy for ischemic stroke. The source of mitochondria, methods for enhancing effectiveness of mitochondrial delivery and transplantation, and the potential mechanism of mitochondrial transplantation therapy for ischemic stroke

Cellular and Molecular NeurobiologyVol. 46(1)
Second Affiliated Hospital of Xi'an Jiaotong University (CN), Xijing Hospital (CN), Air Force Medical University (CN)
Good health and well-being
Openalex Percentile: Top 66%
Mitochondrial Function and Pathology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.