Strain Differences in Neointimal Hyperplasia in the Rat

Author:

Assadnia Shahin1,Rapp John P.1,Nestor Andrea L.1,Pringle Timothy1,Cerilli Greg J.1,Gunning William T.1,Webb Thomas H.1,Kligman Mark1,Allison David C.1

Affiliation:

1. From the Departments of Surgery (S.A., A.L.N., T.P., G.J.C., T.H.W., M.K., D.C.A.), Physiology and Molecular Medicine (J.P.R., D.C.A.), and Pathology (W.T.G.), Medical College of Ohio, Toledo.

Abstract

Abstract —We performed an initial screen of 11 rat strains by use of a standard balloon injury to the left iliac artery to observe whether genetically determined differences existed in the development of neointimal hyperplasia. Neointimal hyperplasia was assayed 8 weeks after the vascular injury on coded microscopic sections. Statistically significant differences in the percentages of the vascular wall cross-sectional areas composed of intima (percentage intima) secondary to neointimal hyperplasia were noted among the different rat strains ( P <0.02), with the Brown-Norway (BN), Dark Agouti, and Milan normotensive strain rats having the highest and the spontaneously hypertensive rats (SHR) having the lowest percentages of intima. In a separate experiment, F 1 hybrids of SHR×BN strains and parental BN and SHR underwent the vascular injury, and the parental strains again showed a statistically significant difference from one another in the mean percentage of intima ( P <0.0001). The F 1 hybrids showed an average percentage of intima intermediate between those of the parental strains. The average lumen size of the injured BN vessels were significantly smaller than that of the noninjured control vessels ( P =0.044), but this significance disappeared when the circular areas of these vessels were calculated without taking neointimal growth into consideration ( P =0.649). These results provide the groundwork for a genetic linkage analysis to identify the genes that influence the development of neointimal hyperplasia after vascular injury.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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