Homocyst(e)ine accumulation in pigs fed diets deficient in vitamin B-6: relationship to atherosclerosis.

The early onset of atherosclerotic lesions in homocystinuric individuals has implicated homocyst(e)ine in the development of atherosclerosis. Two trials were conducted in which diets totally or partially deficient in vitamin B-6 were fed to pigs to investigate the accumulation of homocyst(e)ine in the plasma and the development of vascular lesions. In one trial plasma free homocyst(e)ine levels were 179 and 43 mumol/liter in deficient and adequate pigs, respectively, on day 24, while cysteine levels were 39 and 155 mumol/liter. The concentration of plasma protein-bound homocysteine and cysteine reflected the plasma-free values. Because pigs deficient in pyridoxine could be used only over short time intervals, pigs in trial 2 received 0, 0.03, 0.3 or 3 mg (i.e., 0, 2, 20 or 200% of allowance) of supplemental pyridoxine . HCl per kilogram diet. After 12 weeks pigs deficient and adequate in vitamin B-6 were injected intravenously with Evan's blue dye and the vascular trunk perfused with 2% glutaraldehyde. The aorta and major organs were removed and examined for vascular lesions. Grossly no significant lesions were seen. Light microscopy revealed occasional foci of intimal degeneration and mural thickening in the renal arterioles of pigs deficient in vitamin B-6. An area of focal medial necrosis was observed in one of the pigs deficient in vitamin B-6. Pigs fed diets containing 0.03 mg pyridoxine . HCl per kilogram diet had homocyst(e)ine concentrations not different from pigs fed diets with no added pyridoxine. Animals fed diets containing 0.3 mg pyridoxine . HCl per kilogram had homocyst(e)ine concentrations slightly higher than controls fed 3.0 mg/kg. Feed intake and weight gain increased with increasing pyridoxine in the diet. Swine offer an excellent vascular model for humans. Diets partially deficient in vitamin B-6 which cause the homocyst(e)ine concentration to increase, but allow better growth and feed consumption than diets totally deficient in pyridoxine, could be fed to pigs to study homocyst(e)ine-induced vascular damage over extended period of time.