Peptides Evaluated In Silico, In Vitro, and In Vivo as Therapeutic Tools for Obesity: A Systematic Review

被引:2
作者
Aguiar, Ana Julia Felipe Camelo [1 ]
de Medeiros, Wendjilla Fortunato [2 ]
da Silva-Maia, Juliana Kelly [2 ,3 ]
Bezerra, Ingrid Wilza Leal [3 ]
Piuvezam, Grasiela [4 ,5 ]
Morais, Ana Heloneida de Araujo [1 ,2 ,3 ]
机构
[1] Univ Fed Rio Grande do Norte, Biosci Ctr, Biochem & Mol Biol Postgrad Program, BR-59078970 Natal, RN, Brazil
[2] Univ Fed Rio Grande do Norte, Ctr Hlth Sci, Nutr Postgrad Program, BR-59078900 Natal, RN, Brazil
[3] Univ Fed Rio Grande do Norte, Ctr Hlth Sci, Dept Nutr, BR-59078900 Natal, RN, Brazil
[4] Univ Fed Rio Grande do Norte, Ctr Hlth Sci, Hlth Sci Postgrad Program, BR-59078900 Natal, RN, Brazil
[5] Univ Fed Rio Grande do Norte, Publ Hlth Dept, BR-59078970 Natal, RN, Brazil
关键词
anti-obesity agent; obesity management; computer simulation; molecular dynamics simulation; molecular docking; peptides; molecular conformation; obesity; PROTEIN HYDROLYSATE; WEIGHT-LOSS; MANAGEMENT; PROGRAM; ADULTS; ALPHA;
D O I
10.3390/ijms25179646
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bioinformatics has emerged as a valuable tool for screening drugs and understanding their effects. This systematic review aimed to evaluate whether in silico studies using anti-obesity peptides targeting therapeutic pathways for obesity, when subsequently evaluated in vitro and in vivo, demonstrated effects consistent with those predicted in the computational analysis. The review was framed by the question: "What peptides or proteins have been used to treat obesity in in silico studies?" and structured according to the acronym PECo. The systematic review protocol was developed and registered in PROSPERO (CRD42022355540) in accordance with the PRISMA-P, and all stages of the review adhered to these guidelines. Studies were sourced from the following databases: PubMed, ScienceDirect, Scopus, Web of Science, Virtual Heath Library, and EMBASE. The search strategies resulted in 1015 articles, of which, based on the exclusion and inclusion criteria, 7 were included in this systematic review. The anti-obesity peptides identified originated from various sources including bovine alpha-lactalbumin from cocoa seed (Theobroma cacao L.), chia seed (Salvia hispanica L.), rice bran (Oryza sativa), sesame (Sesamum indicum L.), sea buckthorn seed flour (Hippophae rhamnoides), and adzuki beans (Vigna angularis). All articles underwent in vitro and in vivo reassessment and used molecular docking methodology in their in silico studies. Among the studies included in the review, 46.15% were classified as having an "uncertain risk of bias" in six of the thirteen criteria evaluated. The primary target investigated was pancreatic lipase (n = 5), with all peptides targeting this enzyme demonstrating inhibition, a finding supported both in vitro and in vivo. Additionally, other peptides were identified as PPAR gamma and PPAR alpha agonists (n = 2). Notably, all peptides exhibited different mechanisms of action in lipid metabolism and adipogenesis. The findings of this systematic review underscore the effectiveness of computational simulation as a screening tool, providing crucial insights and guiding in vitro and in vivo investigations for the discovery of novel anti-obesity peptides.
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页数:26
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