OBJECTIVE This study evaluates the role of Gelation metnacrylate(GelMA)hydrogel loaded with hPT H(3-34)(29-34)short peptide in the healing of chronic infectious skin wounds in diabetic rats.METHODS Ex-perimental rats were divided into control group,GelMA group and GelM A+hPTH(3-34)(29-34)group,with 15 rats in each group.Diabetic rat models were prepared,and chronic infectious skin wounds were constructed.Differences in wound area changes,wound healing-related indicator[type Ⅰ collagen α1 chain(COL1A1),α-smooth muscle actin(α-SMA),platelet endothelial cell adhesion molecule-1(CD31),matrix metalloproteinase-9(MMP9)and cyclooxygenase-2(Cox2)]expression and migration ability of fibroblasts in vitro were compared a-mong the groups.RESULTS Compared with the control group,the wound area of rats in the GelMA group de-creased on Day 7 and Day 14(P＜0.05),and the wound area of rats in the GelM A+hPTH(3-34)(29-34)group decreased on Day 3,Day 7 and Day 14(P＜0.05).Compared with the GelMA group,the wound area of rats in the GelM A+hPTH(3-34)(29-34)group decreased on Day 3,Day 7 and Day 14(P＜0.05).Compared with the control group,on Day 7 after modeling,the expression of COL1A1,α-SMA and CD31 in rats was upregulated,and in the GelM A+hPTH(3-34)(29-34)group showed a greater increase than in the GelMA group(P＜0.05),while the expression of MMP9 and Cox2 was downregulated,and in the GelMA+hPTH(3-34)(29-34)group showed a greater decrease than in the GelMA group(P＜0.05).Compared with the control group,on Day 7 af-ter modeling,the relative activity of NLRP3,IL-6,TNF-α,IL-1β and Caspase-1 in rats decreased,and in the GelM A+hPTH(3-34)(29-34)group showed a greater decrease than in the GelMA group(P＜0.05).On Day 7 after modeling,the relative scratch distance of fibroblasts derived from the wound tissue in the GelMA+h PT H(3-34)(29-34)group was greater than that in the GelMA group,which was greater than that in the control group(P＜0.05).CONCLUSIONS The GelMA hydrogel loaded with hPTH(3-34)(29-34)short peptide can effectively accelerate the wound healing process and enhance tissue repair and structural reconstruction by inhibiting the activ-ity of the NLRP3 inflammasome pathway,demonstrating its potential to improve wound healing efficiency.

OBJECTIVE This study evaluates the role of Gelation metnacrylate(GelMA)hydrogel loaded with hPT H(3-34)(29-34)short peptide in the healing of chronic infectious skin wounds in diabetic rats.METHODS Ex-perimental rats were divided into control group,GelMA group and GelM A+hPTH(3-34)(29-34)group,with 15 rats in each group.Diabetic rat models were prepared,and chronic infectious skin wounds were constructed.Differences in wound area changes,wound healing-related indicator[type Ⅰ collagen α1 chain(COL1A1),α-smooth muscle actin(α-SMA),platelet endothelial cell adhesion molecule-1(CD31),matrix metalloproteinase-9(MMP9)and cyclooxygenase-2(Cox2)]expression and migration ability of fibroblasts in vitro were compared a-mong the groups.RESULTS Compared with the control group,the wound area of rats in the GelMA group de-creased on Day 7 and Day 14(P＜0.05),and the wound area of rats in the GelM A+hPTH(3-34)(29-34)group decreased on Day 3,Day 7 and Day 14(P＜0.05).Compared with the GelMA group,the wound area of rats in the GelM A+hPTH(3-34)(29-34)group decreased on Day 3,Day 7 and Day 14(P＜0.05).Compared with the control group,on Day 7 after modeling,the expression of COL1A1,α-SMA and CD31 in rats was upregulated,and in the GelM A+hPTH(3-34)(29-34)group showed a greater increase than in the GelMA group(P＜0.05),while the expression of MMP9 and Cox2 was downregulated,and in the GelMA+hPTH(3-34)(29-34)group showed a greater decrease than in the GelMA group(P＜0.05).Compared with the control group,on Day 7 af-ter modeling,the relative activity of NLRP3,IL-6,TNF-α,IL-1β and Caspase-1 in rats decreased,and in the GelM A+hPTH(3-34)(29-34)group showed a greater decrease than in the GelMA group(P＜0.05).On Day 7 after modeling,the relative scratch distance of fibroblasts derived from the wound tissue in the GelMA+h PT H(3-34)(29-34)group was greater than that in the GelMA group,which was greater than that in the control group(P＜0.05).CONCLUSIONS The GelMA hydrogel loaded with hPTH(3-34)(29-34)short peptide can effectively accelerate the wound healing process and enhance tissue repair and structural reconstruction by inhibiting the activ-ity of the NLRP3 inflammasome pathway,demonstrating its potential to improve wound healing efficiency.