This review highlights the mechanistic basis of Micro Zhēngjiǎ lesions in diabetic myocardial fibrosis and proposes Huoxue-Tongluo therapy as a potential translational treatment.
Diabetic myocardial fibrosis (DMF) is a prominent pathological process that leads to the progression of diabetic heart disease, and yet the underlying mechanisms have not been properly clarified. Recently, a new paradigm called Micro Zhēngjiǎ lesion has been implicated, with microstructural changes in the myocardial capillaries being indicated as critical factors in the development of diabetic fibrosis. The purpose of the review is to investigate the mechanistic basis of the Micro Zhēngjiǎ lesion in DMF and its implications across tissue, cellular, and molecular levels. This article summarizes findings from histological and imaging studies, which show the structural and functional impairments of the myocardial extracellular space, as well as dysregulation of fibrosis-related signaling pathways, in the diabetic heart. Moreover, potential treatment interventions are reviewed, especially Huoxue-Tongluo therapy. This approach, which aims to activate blood circulation and dredge collaterals, combines traditional Chinese medicine with modern pharmacological principles to reverse the development of DMF. By targeting major inflammatory mediators, improving microcirculation, and regulating fibroblast activation, Huoxue-Tongluo therapy has the potential to be used as an alternative or complementary approach to conventional therapy. The review proves the translational potential of the given therapeutic paradigm and suggests future research directions to investigate the multifaceted interplay of microstructural lesions, metabolic dysfunction, and fibrosis in the diabetic heart in depth.
yilin wang (Thu,) studied this question.