Effects of GHK peptide and its structure analogues, D-Ala-GHK AND GHK-D-Ala, on innate immunity and lipid peroxidation processes in skin wound

Kamila K. Rakhmetova, I. Bobyntsev, A. Bezhin, Maksim E. Dolgintsev, A. O. Vorvul
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Abstract

Objective: to study the effects of the GHK peptide and its structure analogues on the mechanisms of innate immunity and lipid peroxidation in wound. Materials and methods. The experiments were performed on 70 male Wistar rats. The skin wound was modeled by applying a full-layer wound with an area of 250 mm2 on the animal's back. The peptides Gly-His-Lys (GHK), D-Ala-Gly-His-Lys (D-Ala-GHK), and Gly-His-Lys-D-Ala (GHK-D-Ala) were used in doses of 0.5 μg/kg and 1.5 μg/kg, which it was administered intradermally in doses of 0.5 μg/kg and 1.5 μg/kg in a volume of 0.1 ml for 3, 7 or 10 days. The activity of lipid peroxidation (LPO) processes in blood serum was assessed by the content of malonic dialdehyde (MDA) and acylhydroperoxides (AHP). The antioxidant mechanisms were evaluated by determining the activity of catalase and the total antioxidant activity (OAA) of blood serum. Phagocytic activity of blood neutrophils was assessed by phagocytic index (PI) and phagocytic number (PN). The activity of oxygen-dependent mechanisms in phagocytes was evaluated in a spontaneous nitroblue tetrazolium test (NBT). Results. After the administration of GHK, the tendency to PI, PN and completeness of phagocytosis prevailed, which mainly persisted with the use of peptides D-Ala-GHK and GHK-D-Ala. At the same time, the GHK-D-Ala peptide at a dose of 1.5 μg/kg had the most stable effect on phagocytic activity. The data obtained in the NBT are largely consistent with the PN indicators. At the same time, the effects of structural analogues, unlike GHK, were manifested throughout the experiment. Significantly significant changes in the activity of LPO and antioxidant mechanisms were observed with the use of all peptides. However, their dynamics, orientation and severity throughout the experiment were quite complex. Conclusion. GHK and its structural analogues, D-Ala-GHK and GHK-D-Ala, had an effect on the indicators of innate immunity and LPO in a skin wound, the severity and direction of which depends on the healing period. At the same time, the most pronounced and stable effects were observed when using GHK-D-Ala. That demonstrates the importance of protecting the tripeptide molecule from the action of carboxypeptidases.
GHK肽及其结构类似物D-Ala-GHK和GHK- d - ala对皮肤创面先天免疫和脂质过氧化过程的影响
目的:研究GHK肽及其结构类似物在创面先天免疫和脂质过氧化机制中的作用。材料和方法。实验以70只雄性Wistar大鼠为实验对象。通过在动物背部涂抹面积为250 mm2的全层伤口来模拟皮肤伤口。肽Gly-His-Lys (GHK)、D-Ala-Gly-His-Lys (D-Ala-GHK)和Gly-His-Lys- d - ala (GHK- d - ala)分别以0.5 μg/kg和1.5 μg/kg的剂量给药,以0.1 ml的体积分别给药3、7和10 d。采用丙二醛(MDA)和酰基过氧化物(AHP)含量测定血清脂质过氧化(LPO)过程的活性。通过测定过氧化氢酶活性和血清总抗氧化活性(OAA)来评价其抗氧化机制。采用吞噬指数(Phagocytic index, PI)和吞噬数(Phagocytic number, PN)评价血液中性粒细胞的吞噬活性。在自发硝基蓝四氮唑试验(NBT)中评估了吞噬细胞中氧依赖机制的活性。结果。GHK给药后,吞噬倾向于PI、PN和完全吞噬,主要与肽D-Ala-GHK和GHK- d - ala的使用有关。同时,1.5 μg/kg剂量的GHK-D-Ala肽对吞噬活性的影响最为稳定。在NBT中获得的数据与PN指标基本一致。与此同时,与GHK不同,结构类似物的作用在整个实验过程中都得到了体现。所有多肽均显著改变了LPO活性和抗氧化机制。然而,在整个实验过程中,它们的动态、方向和严重程度是相当复杂的。结论。GHK及其结构类似物D-Ala-GHK和GHK- d - ala对皮肤创面的先天免疫和LPO指标有影响,影响的严重程度和方向取决于愈合期。同时,使用GHK-D-Ala的效果最为显著和稳定。这证明了保护三肽分子免受羧基肽酶作用的重要性。
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