Literature DB >> 34366874

Corrigendum: Exploring the Mechanism of Total Flavonoids of Drynariae Rhizoma to Improve Large Bone Defects by Network Pharmacology and Experimental Assessment.

Weipeng Sun1, Minying Li2, Lei Xie3, Zhexing Mai4, Yan Zhang1, Lieliang Luo1, Zijian Yan1, Zige Li1, Hang Dong5, Feng Huang5, Zhen Shen6, Ziwei Jiang5.   

Abstract

[This corrects the article DOI: 10.3389/fphar.2021.603734.].
Copyright © 2021 Sun, Li, Xie, Mai, Zhang, Luo, Yan, Li, Dong, Huang, Shen and Jiang.

Entities:  

Keywords:  drynariae rhizoma; experimental assessment; gusuibu; large bone defects; network pharmacology

Year:  2021        PMID: 34366874      PMCID: PMC8343127          DOI: 10.3389/fphar.2021.739503

Source DB:  PubMed          Journal:  Front Pharmacol        ISSN: 1663-9812            Impact factor:   5.810


In the original article, there was a mistake in the legend for Figure 8 and Figure 9 as published. In Figure 8, the numbering of figure legends was incorrect. In Figure 9, the description of previous Figure 9 was not detailed enough. The correct legends appear below.
FIGURE 9

The expressions of p38 MAPK, BMP-2, VEGF, HIF-1α, and RUNX-2 mRNA on BMSCs by quantitative real-time PCR. The data are expressed as the mean ± SEM of three independent experiments. *p < 0.05 vs. control group, # p < 0.05 vs. the TFDR low dosage group, TFDR high dosage group. (B) (a) p38 MAPK, p-p38 MAPK, BMP-2, RUNX-2, VEGF, and HIF-1αprotein expression on BMSCs detected by western blot analysis. (b)–(g) were statistical analysis of (a). The data are expressed as the mean ± SEM of three independent experiments. *p < 0.01 vs. the Control group; # p < 0.01 vs. the TFDR low dosage group.

“FIGURE 8 | Representative images of BMSCs with the alizarin red staining to determine the mineralized nodules. (A) Control group; (B) TFDR low dosage group; (C) TFDR medium dosage group; (D) TFDR high dosage group; (E) The mineralized nodules at each time point of the control group, TFDR low dosage group, TFDR medium dosage group, and TFDR high dosage group were evaluated. The data are expressed as the mean ± SEM of three independent experiments. # p < 0.05 vs. control group, Δ p < 0.05 vs. TFDR low dosage group, ▲ p < 0.05 vs. TFDR high dosage group.” “FIGURE 9 | The expressions of p38 MAPK, BMP-2, VEGF, HIF-1α, and RUNX-2 mRNA on BMSCs by quantitative real-time PCR. The data are expressed as the mean ± SEM of three independent experiments. *p < 0.05 vs. control group, # p < 0.05 vs. the TFDR low dosage group, TFDR high dosage group. (B) (a) p38 MAPK, p-p38 MAPK, BMP-2, RUNX-2, VEGF, and HIF-1αprotein expression on BMSCs detected by western blot analysis. (b)–(g) were statistical analysis of (a). The data are expressed as the mean ± SEM of three independent experiments. *p < 0.01 vs. the Control group; # p < 0.01 vs. the TFDR low dosage group.” In addition, there was a mistake in Figure 3, Figure 7 and Figure 9 as published. The authors uploaded the wrong version of Figure 3 and Figure 7, and uploaded the previous version of Figure 9 by mistake. The corrected Figure 3, Figure 7 and Figure 9 appear below.
FIGURE 3

Evaluation of radiological, micro-CT images, angiogenesis of tibial bone repair of five groups (A). Radiological evaluation of bone repair (A) (a). Representative radiographs of bone repair of the five groups at 12 weeks after surgery (n = 3 per group); (A) (b). Quantitative analysis of radiographic scores (B). Representative micro-CT images of bone repair (B) (a). Three-dimensional reconstructed images of bone defects at 12 weeks after surgical dotted boxes indicate region of interest (ROI), representing bone distracted gaps (n = 3 per group); (B) (b). Quantification of bone tissue volume/total tissue volume and (BV/TV) insides bone distracted regions (C). Evaluation of angiogenesis within the distracted gaps at 4 weeks after surgery (C) (a). Representative angiographs of the distracted gaps in the five groups (n = 3 per group) (C) (b). Quantification of vessel volume within the distracted regions (yellow dotted boxes indicate region of interest (ROI), representing bone distracted gaps). The data are expressed as the mean ± SEM of three independent experiments. *p < 0.05, compared with the control group; # p < 0.05, compared with the model group; Δ p < 0.05, compared the difference of the medium dose with the low and high doses in the TFDR group.

FIGURE 7

The ALP staining assay is performed to evaluate ALP activity after incubated for 10 days (A). TFDR low dosage group; (B). TFDR medium dosage group; (C). TFDR high dosage group; control group; (D). control group (E). The ALP activity at each time point of the control group, TFDR low dosage group, TFDR medium dosage group, and TFDR high dosage group. The data are expressed as the mean ± SEM of three independent experiments. # p < 0.05 vs. control group, Δ p < 0.05 vs. TFDR low dosage group, ▲ p < 0.05 vs. TFDR high dosage group.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated. Evaluation of radiological, micro-CT images, angiogenesis of tibial bone repair of five groups (A). Radiological evaluation of bone repair (A) (a). Representative radiographs of bone repair of the five groups at 12 weeks after surgery (n = 3 per group); (A) (b). Quantitative analysis of radiographic scores (B). Representative micro-CT images of bone repair (B) (a). Three-dimensional reconstructed images of bone defects at 12 weeks after surgical dotted boxes indicate region of interest (ROI), representing bone distracted gaps (n = 3 per group); (B) (b). Quantification of bone tissue volume/total tissue volume and (BV/TV) insides bone distracted regions (C). Evaluation of angiogenesis within the distracted gaps at 4 weeks after surgery (C) (a). Representative angiographs of the distracted gaps in the five groups (n = 3 per group) (C) (b). Quantification of vessel volume within the distracted regions (yellow dotted boxes indicate region of interest (ROI), representing bone distracted gaps). The data are expressed as the mean ± SEM of three independent experiments. *p < 0.05, compared with the control group; # p < 0.05, compared with the model group; Δ p < 0.05, compared the difference of the medium dose with the low and high doses in the TFDR group. The ALP staining assay is performed to evaluate ALP activity after incubated for 10 days (A). TFDR low dosage group; (B). TFDR medium dosage group; (C). TFDR high dosage group; control group; (D). control group (E). The ALP activity at each time point of the control group, TFDR low dosage group, TFDR medium dosage group, and TFDR high dosage group. The data are expressed as the mean ± SEM of three independent experiments. # p < 0.05 vs. control group, Δ p < 0.05 vs. TFDR low dosage group, ▲ p < 0.05 vs. TFDR high dosage group. The expressions of p38 MAPK, BMP-2, VEGF, HIF-1α, and RUNX-2 mRNA on BMSCs by quantitative real-time PCR. The data are expressed as the mean ± SEM of three independent experiments. *p < 0.05 vs. control group, # p < 0.05 vs. the TFDR low dosage group, TFDR high dosage group. (B) (a) p38 MAPK, p-p38 MAPK, BMP-2, RUNX-2, VEGF, and HIF-1αprotein expression on BMSCs detected by western blot analysis. (b)–(g) were statistical analysis of (a). The data are expressed as the mean ± SEM of three independent experiments. *p < 0.01 vs. the Control group; # p < 0.01 vs. the TFDR low dosage group.
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Authors:  A Fioravanti; S Tenti; S Cheleschi
Journal:  Front Pharmacol       Date:  2022-05-03       Impact factor: 5.988

  1 in total

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