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骨质疏松症发病机制和治疗策略的研究进展。

Advances in pathogenesis and therapeutic strategies for osteoporosis.

机构信息

College of Pharmacy, Shenzhen Technology University, Shenzhen 518118, PR China.

Department of Pharmacy, Liyuan Hospital, Tongji Medical School, Huazhong University of Science and Technology, Wuhan, Hubei 430077, PR China.

出版信息

Pharmacol Ther. 2022 Sep;237:108168. doi: 10.1016/j.pharmthera.2022.108168. Epub 2022 Mar 10.

Abstract

Osteoporosis, is the most common bone disorder worldwide characterized by low bone mineral density, leaving affected bones vulnerable to fracture. Bone homeostasis depends on the precise balance between bone resorption by osteoclasts and bone matrix formation by mesenchymal lineage osteoblasts, and involves a series of complex and highly regulated steps. Bone homeostasis will be disrupted when the speed of bone resorption is faster than bone formation. Based on various regulatory mechanisms of bone homeostasis, a series of drugs targeting osteoporosis have emerged in clinical practice, including bisphosphonates, selective estrogen receptor modulators, calcitonin, molecular-targeted drugs and so on. However, many drugs have major adverse effects or are unsuitable for long-term use. Therefore, it is very urgent to find more effective therapeutic drugs based on the new pathogenesis of osteoporosis. In this review, we summarize novel mechanisms involved in the pathological process of osteoporosis, including the roles of gut microbiome, autophagy, iron balance and cellular senescence. Based on the above pathological mechanism, we found promising drugs for osteoporosis treatment, such as: probiotics, alpha-ketoglutarate, senolytics and hydrogen sulfide. This new finding may provide an important basis for elucidating the complex pathological mechanisms of osteoporosis and provide promising drugs for clinical osteoporosis treatment.

摘要

骨质疏松症是全球最常见的骨骼疾病,其特征是骨密度低,使受累骨骼容易骨折。骨骼的动态平衡依赖于破骨细胞对骨的吸收和间充质谱系成骨细胞对骨基质的形成之间的精确平衡,涉及一系列复杂而高度调节的步骤。当骨吸收的速度快于骨形成时,骨骼的动态平衡就会被打破。基于骨骼动态平衡的各种调节机制,临床上出现了一系列针对骨质疏松症的药物,包括双膦酸盐、选择性雌激素受体调节剂、降钙素、分子靶向药物等。然而,许多药物都有严重的不良反应,或者不适合长期使用。因此,基于骨质疏松症的新发病机制,寻找更有效的治疗药物非常紧迫。在这篇综述中,我们总结了骨质疏松症病理过程中涉及的新机制,包括肠道微生物组、自噬、铁平衡和细胞衰老的作用。基于上述病理机制,我们发现了一些有前途的骨质疏松症治疗药物,如益生菌、α-酮戊二酸、衰老细胞清除剂和硫化氢。这一新发现可能为阐明骨质疏松症的复杂病理机制提供重要依据,并为临床骨质疏松症治疗提供有前途的药物。

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