摘要An abnormal inflammatory response is one of the main pathogenic mechanisms of abdominal aortic aneurysms(AAAs),and tranilast,an antiallergic drug,has anti-inflammatory properties.The effect and mechanism of action of tranilast on AAAs remain incompletely defined.To evaluate the preventive and therapeutic effects on experimental AAAs induced by intra-aortic elastase infusion in mice,tranilast was administered either before or after elastase infusion and continued until the experimental endpoint.Bioinformatics analysis and corresponding validation experiments were used to explore the possible mechanisms by which tranilast affects AAA progression.Compared with vehicle treatment,both tra-nilast pre-treatment and post-treatment therapies markedly inhibited aneurysmal aortic expansion.Treatment with tranilast attenuated the degradation of aneurysmal medial elastin and the depletion of smooth muscle cells.Aortic leukocyte accumulation was significantly lower in aneurysmal aortas from tranilast-treated mice than in those from vehicle-treated mice.Mural abnormal angiogenesis and aortic matrix metalloproteinase(MMP)2 and 9 expression levels were also reduced after tranilast treatment.Bioinformatics analysis revealed that nucleotide-binding oligomerization domain-like receptor family protein 3(NLRP3)may be a hub target through which tranilast affects AAAs.NLRP3 expression levels were lower in the aneurysmal aortas of tranilast-treated mice than in those of vehicle-treated elastase-infused mice.Both Nlrp3 deficiency and treatment with the NLRP3 inhibitor MCC950 attenuated experimental AAAs.However,cotreatment with tranilast had no additive or synergistic influence on AAA suppression.Additionally,tranilast treatment reduced caspase 1 cleavage by the NLRP3 inflam-masome and consequently interleukin-1β secretion in peritoneal macrophages in vitro.These findings indicate that the protective effect of tranilast on AAA may be partially mediated by the inhibition of the NLRP3 inflammasome pathway and may represent a potential drug for the treatment of AAA in the clinic.