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International Journal of Molecular Sciences logoLink to International Journal of Molecular Sciences
. 2019 Dec 25;21(1):174. doi: 10.3390/ijms21010174

Correction: Kim, Y. K. et al. Tussilagone Inhibits the Inflammatory Response and Improves Survival in CLP-Induced Septic Mice. Int. J. Mol. Sci. 2017, 18, 2744

Yun Kyu Kim 1,3,, Myeong Gu Yeo 2,, Bo Kang Oh 3, Ha Yeong Kim 3, Hun Ji Yang 3, Seung-Sik Cho 4, Minchan Gil 1,*, Kyung Jin Lee 3,*
PMCID: PMC6981832  PMID: 31881801

We wish to make the following corrections to this paper [1]:

We found that Figure 7A,C data were unintentionally reused from the previously published data [2]. The mistake happened during the preparation of data figures for the revision in the peer-review process. All authors regret that error.

Due to the incorrect figure in original Figure 7A,C, replace the following

graphic file with name ijms-21-00174-i001.jpg

with the corrected Figure 7 (Figure 1)

Figure 1.

Figure 1

Effect of TS on survival and lung injury in cecal ligation and puncture (CLP)-induced septic mice. (A) To examine the effect of TS on the survival of CLP-induced septic mice, survival of mice was then monitored every 24 h for up to 8 days for the following experimental groups (a) sham control; mice were orally administered with either (b) vehicle (corn oil, 0.1 mL per mouse, n = 5), (c) 1 mg/kg TS (n = 5), or (d) 10 mg/kg TS (n = 5), 2 h prior to the operation. Significantly different from CLP-induced septic group (B) Expression of COX-2 and TNF-α transcripts in the isolated PAM were determined by real-time PCR; * p < 0.05 vs. CLP-induced septic group (n = 3 in each group) (C) The lungs from each experimental group were processed for histologic evaluation 1 day after CLP. Representative histologic changes in lung tissue obtained from mice belonging to each group are displayed and the arrows indicate the damaged area (hematoxylin and eosin staining; magnification 400×). Scale bar represents 200 um. (D) The extent of lung injury was estimated using scores in different sections for neutrophil infiltration, hemorrhage, necrosis, congestion, and edema. * p < 0.05 vs. CLP-induced septic group (n = 3 in each group).

We would like to apologize for any inconvenience caused to the readers by these changes.

Conflicts of Interest

The authors declare no conflict of interest.

References

  • 1.Kim Y.K., Yeo M.G., Oh B.K., Kim H.Y., Yang H.J., Cho S.S., Gil M., Lee K.J. Tussilagone Inhibits the Inflammatory Response and Improves Survival in CLP-Induced Septic Mice. Int. J. Mol. Sci. 2017;18:2744. doi: 10.3390/ijms18122744. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Gil M., Kim Y.K., Hong S.B., Lee K.J. Naringin Decreases TNF-α and HMGB1 Release from LPS-Stimulated Macrophages and Improves Survival in a CLP-Induced Sepsis Mice. PLoS ONE. 2016;11:e0164186. doi: 10.1371/journal.pone.0164186. [DOI] [PMC free article] [PubMed] [Google Scholar]

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