Pitchakarn Pornsiri, Buacheen Pensiri, Taya Sirinya, Karinchai Jirarat, Temviriyanukul Piya, Inthachat Woorawee, Chaipoot Supakit, Wiriyacharee Pairote, Phongphisutthinant Rewat, Ounjaijean Sakaewan, Boonyapranai Kongsak
Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Muang Chiang Mai, Chiang Mai 50200, Thailand.
Multidisciplinary Research Institute, Chiang Mai University, Chiang Mai 50200, Thailand.
Foods. 2024 Aug 16;13(16):2558. doi: 10.3390/foods13162558.
Soy protein is considered to be a high-quality protein with a range of important biological functions. However, the applications of soy protein are limited due to its poor solubility and high level of allergenicity. Its peptides have been of interest because they exert the same biological functions as soy protein, but are easier to absorb, more stable and soluble, and have a lower allergenicity. Moreover, recent research found that an attachment of chemical moieties to peptides could improve their properties including their biodistribution, pharmacokinetic, and biological activities with lower toxicity. This study therefore aimed to acquire scientific evidence to support the further application and safe use of the soybean oligopeptide (OT) conjugated with allulose (OT-AL) or D-mannose (OT-Man). The anti-inflammation, cytotoxicity, and genotoxicity of OT, OT-AL, and OT-Man were investigated. The results showed that OT, AL, Man, OT-AL, and OT-Man at doses of up to 1000 µg/mL were not toxic to HepG2 (liver cancer cells), HEK293 (kidney cells), LX-2 (hepatic stellate cells), and pre- and mature-3T3-L1 (fibroblasts and adipocytes, respectively), while slightly delaying the proliferation of RAW 264.7 cells (macrophages) at high doses. In addition, the oligopeptides at up to 800 µg/mL were not toxic to isolated human peripheral blood mononuclear cells (PBMCs) and did not induce hemolysis in human red blood cells (RBCs). OT-Man (200 and 400 µg/mL), but not OT, AL, Man, and OT-AL, significantly reduced the production of NO and the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX2) stimulated by lipopolysaccharide (LPS) in RAW 264.7 cells, suggesting that the mannose conjugation of soy peptide had an inhibitory effect against LPS-stimulated inflammation. In addition, the secretion of interleukin-6 (IL-6) stimulated by LPS was significantly reduced by OT-AL (200 and 400 µg/mL) and OT-Man (400 µg/mL). The tumor necrosis factor-α (TNF-α) level was significantly decreased by OT (400 µg/mL), AL (400 µg/mL), OT-AL (200 µg/mL), and OT-Man (200 and 400 µg/mL) in the LPS-stimulated cells. The conjugation of the peptides with either AL or Man is likely to be enhance the anti-inflammation ability to inhibit the secretion of cytokines. As OT-Man exhibited a high potential to inhibit LPS-induced inflammation in macrophages, its mutagenicity ability was then assessed in bacteria and . These findings showed that OT-Man did not trigger DNA mutations and was genome-safe. This study provides possible insights into the health advantages and safe use of conjugated soybean peptides.
大豆蛋白被认为是一种具有一系列重要生物学功能的优质蛋白质。然而,由于其溶解性差和致敏性高,大豆蛋白的应用受到限制。大豆蛋白的肽类备受关注,因为它们具有与大豆蛋白相同的生物学功能,但更易于吸收、更稳定且溶解性更好,致敏性也更低。此外,最近的研究发现,将化学基团连接到肽上可以改善其性质,包括生物分布、药代动力学和生物活性,同时毒性更低。因此,本研究旨在获取科学证据,以支持与阿洛酮糖(OT-AL)或D-甘露糖(OT-Man)偶联的大豆寡肽(OT)的进一步应用和安全使用。研究了OT、OT-AL和OT-Man的抗炎、细胞毒性和遗传毒性。结果表明,剂量高达1000 µg/mL的OT、AL、Man、OT-AL和OT-Man对HepG2(肝癌细胞)、HEK293(肾细胞)、LX-2(肝星状细胞)以及前3T3-L1和成熟3T3-L1(分别为成纤维细胞和脂肪细胞)无毒,而在高剂量时会略微延迟RAW 264.7细胞(巨噬细胞)的增殖。此外,剂量高达800 µg/mL的寡肽对分离的人外周血单个核细胞(PBMC)无毒,也不会诱导人红细胞(RBC)溶血。OT-Man(200和400 µg/mL),而不是OT、AL、Man和OT-AL,显著降低了脂多糖(LPS)刺激的RAW 264.7细胞中NO的产生以及诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX2)的表达,表明大豆肽与甘露糖的偶联对LPS刺激的炎症具有抑制作用。此外,OT-AL(200和400 µg/mL)和OT-Man(400 µg/mL)显著降低了LPS刺激的白细胞介素-6(IL-6)的分泌。在LPS刺激的细胞中,OT(400 µg/mL)、AL(400 µg/mL)、OT-AL(200 µg/mL)和OT-Man(200和400 µg/mL)使肿瘤坏死因子-α(TNF-α)水平显著降低。肽与AL或Man的偶联可能会增强抑制细胞因子分泌的抗炎能力。由于OT-Man在抑制巨噬细胞中LPS诱导的炎症方面具有很高的潜力,因此随后在细菌中评估了其致突变能力。这些发现表明,OT-Man不会引发DNA突变,是基因组安全的。本研究为偶联大豆肽的健康益处和安全使用提供了可能的见解。