Literature DB >> 29147658

Corrigendum to "Chitosan Prevents Gentamicin-Induced Nephrotoxicity via a Carbonyl Stress-Dependent Pathway".

Chu-Kuang Chou1,2, Yi-Chieh Li3, Shih-Ming Chen3, Yi-Min Shih3, Jen-Ai Lee3.   

Abstract

[This corrects the article DOI: 10.1155/2015/675714.].

Entities:  

Year:  2017        PMID: 29147658      PMCID: PMC5632887          DOI: 10.1155/2017/7686249

Source DB:  PubMed          Journal:  Biomed Res Int            Impact factor:   3.411


In the article titled “Chitosan Prevents Gentamicin-Induced Nephrotoxicity via a Carbonyl Stress-Dependent Pathway” [1], the name of the first author was given incorrectly as Chu-Kung Chou. The author's name should have been written as Chu-Kuang Chou. The revised authors' list is shown above. Also, there was an error in Figure 2. Figures 2(b) and 2(e) were inadvertently reused from Yi-Chieh Li, Yi-Min Shih, and Jen-Ai Lee, “Gentamicin caused renal injury deeply related to methylglyoxal and Nɛ-(carboxyethyl)lysine (CEL),” Toxicology Letters, Volume 219, Issue 1, https://www.doi.org/10.1016/j.toxlet.2013.01.024. Additionally, the same picture of Figure 2(e) was presented as Figure 2(c). The corrected Figure 2 is as follows.
Figure 2

LMWC-induced changes in histology. Light micrographs of rat kidney sections were stained with hematoxylin and eosin. (a) Histology of kidney tissue in the control group. (b) Necrotic tubules and desquamation were apparent after treatment with 150 mg/kg/day GM for 6 days. (c) Treatment of GN rats with 165 mg/kg/day LMWC for 13 days improved histology. (d) Treatment of GN rats with 825 mg/kg/day LMWC for 13 days significantly improved histology. (e) Treatment of GN rats with 100 mg/kg/day metformin for 13 days significantly improved histology.

  1 in total

1.  Chitosan Prevents Gentamicin-Induced Nephrotoxicity via a Carbonyl Stress-Dependent Pathway.

Authors:  Chu-Kuang Chou; Yi-Chieh Li; Shih-Ming Chen; Yi-Min Shih; Jen-Ai Lee
Journal:  Biomed Res Int       Date:  2015-04-12       Impact factor: 3.411

  1 in total

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