| Literature DB >> 35368877 |
Rui Lin1, Fei Mu1, Yao Li2, Jialin Duan1, Meina Zhao1, Yue Guan1, Kedi Liu3, Yang Bai4, Aidong Wen1, Peifeng Wei4, Jingwen Wang1, Miaomiao Xi4,5.
Abstract
[This corrects the article DOI: 10.1155/2021/8840896.].Entities:
Year: 2022 PMID: 35368877 PMCID: PMC8967562 DOI: 10.1155/2022/9763253
Source DB: PubMed Journal: Oxid Med Cell Longev ISSN: 1942-0994 Impact factor: 6.543
Figure 1The metabolic profiles of OPLS-DA between the model and SM-DOO groups based on HPLC-Q-TOF-MS: (a) the score plot of OPLS-DA in a negative mode; (b) the corresponding validation plot based on 200 times permutation tests demonstrated the robustness of the OPLS-DA model in a negative mode; (c) the S-plot of OPLS-DA in a negative mode; (d) the VIP of OPLS-DA in a negative mode; (e) the score plot of OPLS-DA in a positive mode; (f) the corresponding validation plot based on 200 times permutation tests demonstrated the robustness of the OPLS-DA model in a positive mode; (g) the S-plot of OPLS-DA in a positive mode; (h) the VIP of OPLS-DA in a positive mode.
Figure 2Effects of SM-DOO on the AMPK/GLUT4 pathway in heart tissues of pigs. p-AMPK, AMPK, GLUT4, and β-actin protein expressions were measured. The protein signals were quantitated by densitometry, and the graph shows their relative levels. All values are presented as the mean ± SD. ##P < 0:01 vs. sham group; ∗∗P < 0:01 vs. model group.