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  • Author: C. ESNAULT x
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Reduction in the intensity of staining by the Feulgen reaction for DNA has been demonstrated in mammalian spermatids during spermiogenesis (Gledhill, Gledhill, Rigler & Ringertz, 1966) and in spermatozoa during transit through the epididymis (Gledhill, 1966, 1971; Bouters, Esnault, Ortavant & Salisbury, 1967; Bouters, Esnault, Salisbury & Ortavant, 1967). On the other hand, it has been reported that there is a reactivation of the Feulgen reaction for spermatozoa in the female genital tract (Chang, 1959; Esnault, Orgebin-Crist & Ortavant, cited by Orgebin-Crist, 1969). As these variations in the intensity of the Feulgen reaction are not related to changes in DNA concentration as measured by ultraviolet absorption, it is likely that they are due to chemical alteration of deoxyribonucleoprotein (Gledhill et al., 1966).

This paper gives the results of measurements of

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The dna content of individual ejaculated spermatozoa and of spermatozoa recovered from the epididymis and ampulla of fifteen rabbits was measured by means of two microspectrophotometric methods: (i) direct determination of ultra-violet (uv) light absorbed at 260 mμ by unstained spermatozoa, and (ii) determination of visible light absorbed at 560 mμ by Feulgen-stained spermatozoa. The dna determinations in uv light for ejaculated spermatozoa and for those recovered from the male ducts revealed no difference, as contrasted with the results obtained by measuring the Feulgen-stainability. The differences in Feulgen-stainability, i.e. in the quantitative response of spermatozoa to the Feulgen reagent, are attributed to an ageing process in the sperm cells: ampullary spermatozoa yielded significantly lower Feulgen-dna values than those obtained from the epididymis; ligation of the vas deferens resulted in a decrease of the Feulgen-dna content of epididymal spermatozoa; the variable Feulgen-dna content of individual ejaculated spermatozoa is attributed to varying percentages of older sperm cells in the ejaculates.