In Japan, the incidence of breast cancer is increasing every year, and the necessity for breast reconstruction using silicone implants is thus increasing. Such reconstructions result in a foreign body response, with formation of a fibrous capsule and thickening, resulting in capsular contracture during shrinkage, which are often accompanied by marked transformation and pain. The mechanisms underlying this phenomenon are unclear, although one report has described decreased capsular contracture following the use of an implant with a processed surface displaying enhanced ruggedness. The present study examined whether capsular contracture would be decreased by changing the outer structure of the silicone implant. Smooth-and textured-type implants were implanted dorsally in rats. Gross and histopathological examinations (hematoxylin and eosin staining, Masson's trichrome staining, transforming growth factor (TGF)-Ī² -staining, a-smooth muscle actin (Ī±-SMA) staining, and collagen I and III staining) were performed at weeks 1, 2, 4 and 8 after implantation to examine capsule thickness. The textured-type implant showed a thinner capsule than the smooth type at weeks 4 and 8. The fibrous layer of the capsule was particularly thin. Moreover, TGF-Ī² -positive cells decreased gradually with the smooth-type implant, while TGF-Ī² -positive cells remained evident upon histopathological examination of the textured-type implant. For textured-type implants, Ī±-SMA-positive cells gradually decreased and type III collagen fibers predominated, while smooth-type implants showed a gradual increase in Ī±-SMA-positive cells and a predominance of type I collagen fibers. Based on these findings, the characteristics of the capsule for textured implants with irregular surfaces can be summarized as follows: 1) during the early stage after implantation, stronger inflammatory reactions are induced compared with the smooth type, and because the inflammation becomes chronic, remodeling from type III collagen to type I collagen is decreased, resulting in a type III collagen-dominant capsule; and 2) as irregular structures buffer the tension applied to the capsule due to body movement, the degree of increase in Ī±-SMA-positive cells is lower compared with the smooth type. As a result, a thin capsule that is less likely to contract is formed. These factors are mostly responsible for reducing capsular contracture for textured implants.