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CORRECTION article

Front. Pharmacol., 09 October 2024
Sec. Cardiovascular and Smooth Muscle Pharmacology

Corrigendum: Protective effects of inhibition of mitochondrial fission on organ function after sepsis

  • State Key Laboratory of Trauma, Burns and Combined Injury, Shock and Transfusion Department, Research Institute of Surgery, Daping Hospital, Army Medical University, Chongqing, China

A Corrigendum on
Protective effects of inhibition of mitochondrial fission on organ function after sepsis

by Zhu Y, Kuang L, Wu Y, Deng H, She H, Zhou Y, Zhang J, Liu L and Li T (2021). Front. Pharmacol. 12:712489. doi: 10.3389/fphar.2021.712489

In the published article, there was an error in Figure 2 as published. Figure 2A depicts blood flow experiments. Upon comparison, we confirmed the images “Sep” and “Mdivi (1)” in the “kidney” blood flow to be identical images; specifically, the image of “Mdivi (1)” in the “kidney” blood flow was misused. The corrected Figure 2 and its caption appear below.

Figure 2
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Figure 2. Effects of Mdivi-1 on vital organ function in septic rats. (A): blood flow of liver and kidney with the Peri Cam PSI System. (B–D): blood flow of liver, kidney and intestine with laser Doppler imaging. (E): intestinal function (D-lactate). (F): aspartate aminotransferase (AST). (G): kidney function creatinine (Crea). (H): Time-lapse monitoring of mean arterial pressure after Mdivi-1 treatment. After CLP 12 h, the mean arterial blood pressure (MAP) was monitored after administration of 12 min, 30 min, 1, 2, 3, 4, 5 and 6 h by femoral artery intubation. (I, J): Effects of Mdivi-1 on survival in septic rats (n = 16). Rats were randomly divided into five groups, after 6 h of treatment, blood vessels were ligated, muscle and skin layers were sutured, and the average survival time and survival rate of rats within 72 h were observed. **p < 0.01 versus Sham. @p < 0.05 and @@p < 0.01 versus conventional treatment (CT) group. Sham, the control group; Sep, sepsis; CT, conventional treatment. 1: Mdivi-1 (1 mg/kg). 3: Mdivi-1 (3 mg/kg).

In the published article, there was an error in Figure 3 as published. Figure 3C depicts mitochondrial morphology experiments of acutely isolated cardiomyocytes. Upon comparison, we confirmed the images in “CT”and “Mdivi (1)” to be identical images; specifically, the image of “Mdivi (1)” was misused. The corrected Figure 3 and its caption appear below.

Figure 3
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Figure 3. Effects of Mdivi-1 on mitochondrial morphology in septic rats. (A, B): mitochondrial morphology of heart by transmission electron microscope (TEM) and statistical analysis (bar = 500 nm). (C, D): mitochondrial morphology of acute isolation of cardiomyocytes in vitro and statistical analysis (bar = 25 μm). (E, F): mitochondrial morphology of cardiomyocytes and vascular smooth muscle cell by laser confocal microscopy and statistical analysis (bar = 25 μm); (G, H): colocalization of mitochondria and Drp1 (bar = 25 μm). *p < 0.05, **p < 0.01 versus sham or ctrl. @p < 0.05, @@p < 0.01 versus conventional treatment (CT) group.^p < 0.05,^p < 0.01 versus LPS. Sham; the control group; Sep, sepsis; CT, conventional treatment. 1: Mdivi-1 (1 mg/kg). 3: Mdivi-1 (3 mg/kg). H9C2: cardiomyocytes. VSMC: vascular smooth muscle cell. Ctrl: control group. M1: Mdivi-1 (10 μM). M5: Mdivi-1 (50 μM).

The authors apologize for these errors and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: mitochondrial fission, Mdivi-1, Drp1, sepsis, organ function

Citation: Zhu Y, Kuang L, Wu Y, Deng H, She H, Zhou Y, Zhang J, Liu L and Li T (2024) Corrigendum: Protective effects of inhibition of mitochondrial fission on organ function after sepsis. Front. Pharmacol. 15:1493530. doi: 10.3389/fphar.2024.1493530

Received: 09 September 2024; Accepted: 23 September 2024;
Published: 09 October 2024.

Edited and reviewed by:

Gordon Huggins, Tufts University, United States

Copyright © 2024 Zhu, Kuang, Wu, Deng, She, Zhou, Zhang, Liu and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Liangming Liu, liangmingliu@yahoo.com; Tao Li, lt200132@163.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.