Influence of various substrates on the acetylcarnitine:carnitine ratio in motile and immotile human spermatozoa

Journal of Reproduction and Fertility
R GolanL M Lewin

Abstract

Human spermatozoa were incubated in albumin-containing Hepes-buffered modified Ringer's solution, in the presence or absence of externally supplied substrates. The acylated forms of carnitine were identified by bioautography. Incubation of the cells with propionate or n-valerate resulted in increased content of propionylcarnitine, but n-butyrate, isobutyrate, n-valerate, isovalerate, hexanoate or heptanoate did not result in the appearance of acylcarnitine of chain length C4-C7. The addition of methionine, valine or isoleucine (whose catabolic pathways should produce propionyl-CoA) to the incubation medium did not increase propionylcarnitine. In all cases acetylcarnitine was the major acylcarnitine in human spermatozoa. The ratio of acetylcarnitine:carnitine remained relatively constant in spermatozoa incubated without external substrate for up to 4 h. No significant change in the ratio was observed when glucose, fructose or citrate were present in the incubation medium. Sorbitol decreased the ratio slightly and aspartic acid slightly increased it. A more pronounced increase in the ratio was caused by lactate or pyruvate. This increase was observed in motile spermatozoa but not in samples from asthenospermic men, indicating tha...Continue Reading

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