Journal of Vascular Surgery
Volume 28, Issue 5 , Pages 909-918 , November 1998

Hyperhomocysteinemia increases intimal hyperplasia in a rat carotid endarterectomy model

Presented at the Twenty-second Annual Meeting of The Southern Association for Vascular Surgery, Rio Grande, Puerto Rico, Jan 21–24, 1998.

Received 28 January 1998 ,Accepted 22 June 1998.

  • Image Result

    Serum homocysteine levels for homocysteine group (n = 8) and control group (n = 9; *P = .0007).

    Serum homocysteine levels for homocysteine group (n = 8) and control group (n = 9; *P = .0007).

  • Image Result

    Amounts of intimal hyperplasia, expressed as percent stenosis, for homocysteine group (n = 8) and control group (n = 9; *P = .0007).

    Amounts of intimal hyperplasia, expressed as percent stenosis, for homocysteine group (n = 8) and control group (n = 9; *P = .0007).

  • Image Result

    Photomicrograph of elastin-stained rat common carotid artery sections 2 weeks after CEA. Sections A1 and A2, from an animal in the control group, show significantly less neointimal hyperplasia than se

    Photomicrograph of elastin-stained rat common carotid artery sections 2 weeks after CEA. Sections A1 and A2, from an animal in the control group, show significantly less neointimal hyperplasia than sections B1 and B2, from animals in the homocysteine group with elevated homocysteine levels. Magnification was ×10 (A1 and B1) and ×40 (A2 and B2). A2 and B2 are magnified sections of vessels seen in A1 and B1. Darker blue staining near the lumen is identified as area of IH. Note lack of internal elastic lamina in A2 and B2 and partial removal of external elastic lamina in B2. Remaining external elastic lamina is seen as thin black staining line.

  • Image Result
    Linear regression model of serum homocysteine levels and percent stenosis (y = 4.38 + 0.42x; df = 15; r2 = 0.72; P = .0001).

    Linear regression model of serum homocysteine levels and percent stenosis (y = 4.38 + 0.42x; df = 15; r2 = 0.72; P = .0001).

 From the Division of Vascular Surgery, Department of Surgery, and the Department of Pathology (Dr Fink), University of Arkansas for Medical Sciences and Veterans Administration Hospital, and the Division of Molecular Epidemiology (Dr Cooney), National Center for Toxicological Research.

☆☆ Reprint requests: Mohammed M. Moursi, MD, Assistant Professor, Division of Vascular Surgery, VA Medical Center, Vascular Lab (112PV/LR), 4300 W 7th St, Little Rock, AR 72205.

 24/6/92619

PII: S0741-5214(98)70069-2

Journal of Vascular Surgery
Volume 28, Issue 5 , Pages 909-918 , November 1998