State Key Laboratory of Oral Diseases, National Clinical Research Center of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China; Department of Implantology, West China Hospital of Stomatology, Sichuan University, Chengdu, China; Jinjiang out-patient section, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
State Key Laboratory of Oral Diseases, National Clinical Research Center of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China; Department of Implantology, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Bone. 2020 Oct;139:115464. doi: 10.1016/j.bone.2020.115464. Epub 2020 Jun 3.
Diabetes is a chronic systematic disease which results in neuropathy and dysfunctional bone metabolism and microcirculation. Calcitonin gene related peptide (CGRP) is an important neuropeptide that is involved in bone formation and vascular response. This study aimed to elucidate the role of CGRP in diabetic peri-implant angiogenesis and osteogenesis, which is yet to be reported. In vivo, we injected streptozotocin into SD rats to establish an experimental diabetes model. We then implanted 1 mm × 5 mm Ti implants into rat tibiae and injected lentivirus into the bone marrow cavity to overexpress or silence the peri-implant CGRP expression. We also applied overexpression lentivirus and silencing short hair RNA (shRNA) in rat bone marrow mesenchymal stem cells (BMSCs) to investigate the biological effects of CGRP in vitro. Through the investigation of diabetic neurons, blood, and peri-implant bone, we could observe that diabetes led to decreased synthesis and expression of CGRP, and high CGRP expression were only seen in peri-implant tissues in the early-to-middle phase of diabetic bone integration. Microfil perfusion followed by micro-CT analysis showed that the overexpression of CGRP enhanced peri-implant angiogenesis via increased vessel volume and thickness. Regarding osteogenesis, CGRP was found to improve the impaired osseointegration, as observed through micro-CT reconstruction and H&E staining. Similarly, overCGRP alleviated the hyperglycemia-triggered decrease in mineralization, and rescued ALP activity and the mRNA and protein expression of VEGF-A, ALP, and OPN. CGRP also attenuated the high glucose-induced production of reactive oxygen species (ROS). Our results demonstrate the potential promotive role of CGRP in early-to-middle phase of osseointegration, as CGRP could regulate the diabetes-induced dysfunctions in peri-implant angiogenesis and osseointegration. Our study provides a new insight into the diabetic peri-implant vasculature and the potential positive effect of CGRP on diabetic peri-implant vessels and bone.
糖尿病是一种导致神经病变和功能性骨代谢及微循环障碍的慢性系统性疾病。降钙素基因相关肽(CGRP)是一种参与骨形成和血管反应的重要神经肽。本研究旨在阐明 CGRP 在糖尿病种植体周围血管生成和骨生成中的作用,这方面的研究尚未见报道。在体内,我们向 SD 大鼠注射链脲佐菌素建立实验性糖尿病模型。然后,我们将 1mm×5mm 的 Ti 种植体植入大鼠胫骨,并向骨髓腔注射慢病毒以过表达或沉默种植体周围 CGRP 的表达。我们还在大鼠骨髓间充质干细胞(BMSCs)中应用过表达慢病毒和沉默短发夹 RNA(shRNA)来研究 CGRP 的生物学效应。通过对糖尿病神经元、血液和种植体周围骨的研究,我们观察到糖尿病导致 CGRP 的合成和表达减少,只有在糖尿病骨整合的早中期,种植体周围组织中才会出现高 CGRP 表达。微灌注后微 CT 分析显示,CGRP 的过表达通过增加血管容积和厚度来增强种植体周围血管生成。关于成骨作用,我们发现 CGRP 改善了受损的骨整合,这可以通过微 CT 重建和 H&E 染色观察到。同样,过表达 CGRP 缓解了高血糖引起的矿化减少,并挽救了碱性磷酸酶(ALP)活性以及血管内皮生长因子 A(VEGF-A)、ALP 和骨桥蛋白(OPN)的 mRNA 和蛋白表达。CGRP 还减轻了高血糖诱导的活性氧(ROS)产生。我们的结果表明,CGRP 在骨整合的早中期具有促进作用,因为 CGRP 可以调节种植体周围血管生成和骨整合中糖尿病引起的功能障碍。我们的研究为糖尿病种植体周围血管提供了新的见解,并为 CGRP 对糖尿病种植体周围血管和骨骼的潜在积极作用提供了新的见解。