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通过从 3D 打印支架中输送钙通道阻滞剂来抑制交感神经激活,以促进骨缺损修复。

Inhibition of Sympathetic Activation by Delivering Calcium Channel Blockers from a 3D Printed Scaffold to Promote Bone Defect Repair.

机构信息

Shanghai Engineering Research Center of Nano-Biomaterials and Regenerative Medicine, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, 201620, China.

出版信息

Adv Healthc Mater. 2022 Aug;11(16):e2200785. doi: 10.1002/adhm.202200785. Epub 2022 Jun 19.

Abstract

Enhancing osteogenesis by promoting neural network reconstruction and neuropeptide release is considered to be an attractive strategy for repairing of critical size bone defects. However, traumatic bone defects often activate the damaged sympathetic nervous system (SNS) in the defect area and release excessive catecholamine to hinder bone defect repair. Herein, a 3D printed scaffold loaded with the calcium channel blocker-nifedipine is proposed to reduce the concentration of catecholamine present in the bone defect region and to accelerate bone healing. To this end, nifedipine-loaded ethosome and laponite are added into a mixed solution containing sodium alginate, methacrylated gelatin, and bone mesenchymal stem cells (BMSCs) to prepare a cell-laden scaffold using 3D bioprinting. The released nifedipine is able to close the calcium channels of nerve cells, thereby blocking sympathetic activation and ultimately inhibiting the release of catecholamine by sympathetic nerve cells, which further promotes the osteogenic differentiation and migration of BMSCs, inhibits osteoclastogenesis in vitro, and effectively improves bone regeneration in a rat critical-size calvarial defect model. Therefore, the results suggest that sustained release of nifedipine from the scaffold can effectively block SNS activation, providing promising strategies for future treatment of bone defects.

摘要

通过促进神经网络重建和神经肽释放来增强成骨作用被认为是修复临界尺寸骨缺损的一种有吸引力的策略。然而,创伤性骨缺损通常会激活缺损区域受损的交感神经系统 (SNS) 并释放过多的儿茶酚胺来阻碍骨缺损修复。在此,提出了一种负载钙通道阻滞剂硝苯地平的 3D 打印支架,以降低骨缺损区域儿茶酚胺的浓度并加速骨愈合。为此,将负载硝苯地平的醇质体和皂土添加到含有海藻酸钠、甲基丙烯酰化明胶和骨髓间充质干细胞 (BMSCs) 的混合溶液中,使用 3D 生物打印制备负载细胞的支架。释放的硝苯地平能够关闭神经细胞的钙通道,从而阻断交感神经的激活,最终抑制交感神经细胞释放儿茶酚胺,这进一步促进了 BMSCs 的成骨分化和迁移,抑制体外破骨细胞的形成,并有效改善大鼠临界尺寸颅骨缺损模型中的骨再生。因此,研究结果表明,支架中硝苯地平的持续释放可以有效阻断 SNS 的激活,为骨缺损的未来治疗提供了有前景的策略。

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