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Recently, the physiological effects of endogenous SO<jats:sub>2<\/jats:sub> were confirmed. Vascular structural remodeling (VSR), an important pathological change in many cardiovascular diseases, plays a crucial role in the pathogenesis of the diseases. Here, the authors reviewed the research progress of endogenous SO<jats:sub>2<\/jats:sub> in regulating VSR by searching the relevant data from PubMed and Medline. In spontaneously hypertensive rats (SHRs) and pulmonary hypertensive rats, SO<jats:sub>2<\/jats:sub>\/aspartate aminotransferase (AAT) pathway was significantly altered. SO<jats:sub>2<\/jats:sub> inhibited vascular smooth muscle cell (VSMC) proliferation, promoted apoptosis, inhibited the synthesis of extracellular collagen but promoted its degradation, and enhanced antioxidative capacity, thereby playing a significant role in attenuating VSR. However, the detailed mechanisms needed to be further explored. Further studies in this field would be important for the better understanding of the pathogenesis of systemic hypertension and pulmonary hypertension. Also, clinical trials are needed to demonstrate if SO<jats:sub>2<\/jats:sub> would be a potential therapeutic target in cardiovascular diseases.<\/jats:p>","DOI":"10.1155\/2016\/4529060","type":"journal-article","created":{"date-parts":[[2016,9,18]],"date-time":"2016-09-18T21:00:53Z","timestamp":1474232453000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":26,"title":["Role of Endogenous Sulfur Dioxide in Regulating Vascular Structural Remodeling in 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