1969Poultry ScienceOpen access

The Influence of Hen Oviduct Homogenates on the Motility, Oxygen Uptake and Fertilizing Capacity of Fowl Spermatozoa

A.R. Lehrer, H Schindler

Open full text 10 citations

Abstract

THE fertilizing capacity of fowl spermatozoa is preserved in the hen oviduct for 8–28 days (Parkes, 1960). It can reasonably be assumed that the preservation is connected with some influence of the oviducal tissue on the metabolism of the stored spermatozoa. This assumption is supported by the finding that fowl spermatozoa had an increased rate of oxygen uptake in vitro after they had been incubated in the hen oviduct in vivo (Hamner and Williams, 1963). A similar effect was also obtained in vitro with spermatozoa suspended in oviduct extracts (Ogasawara and Lorenz, 1964). In the present work, fresh homogenates from different regions of the hen oviduct were used in order to study their influence on both the rate of oxygen uptake and the preservation of motility and fertilizing capacity of fowl spermatozoa. For this purpose, the uterovaginal junction and the infundibulum were chosen because they are known to be…

About this research paper

What this paper is about

THE fertilizing capacity of fowl spermatozoa is preserved in the hen oviduct for 8–28 days (Parkes, 1960). It can reasonably be assumed that the preservation is connected with some influence of the oviducal tissue on the metabolism of the stored spermatozoa. This assumption is supported by the finding that fowl spermatozoa had an increased rate of oxygen uptake in vitro after they had been incubated in the hen oviduct in vivo (Hamner and Williams, 1963). A similar effect was also obtained in vitro with spermatozoa suspended in oviduct extracts (Ogasawara and Lorenz, 1964). In the present work, fresh homogenates from different regions of the hen oviduct were used in order to study their influence on both the rate of oxygen uptake and the preservation of motility and fertilizing capacity of fowl spermatozoa. For this purpose, the uterovaginal junction and the infundibulum were chosen because they are known to be…

Why it matters

OpenAlex reports 10 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

THE fertilizing capacity of fowl spermatozoa is preserved in the hen oviduct for 8–28 days (Parkes, 1960). It can reasonably be assumed that the preservation is connected with some influence of the oviducal tissue on the metabolism of the stored spermatozoa. This assumption is supported by the finding that fowl spermatozoa had an increased rate of oxygen uptake in vitro after they had been incubated in the hen oviduct in vivo (Hamner and Williams, 1963). A similar effect was also obtained in vitro with spermatozoa suspended in oviduct extracts (Ogasawara and Lorenz, 1964). In the present work, fresh homogenates from different regions of the hen oviduct were used in order to study their influence on both the rate of oxygen uptake and the preservation of motility and fertilizing capacity of fowl spermatozoa. For this purpose, the uterovaginal junction and the infundibulum were chosen because they are known to be…

Key concepts: Oviduct, Fowl, Infundibulum, Motility, Biology, In vitro, In vivo, Andrology

Related papers

Back to paper searchBrowse research topicsOriginal source
The Influence of Hen Oviduct Homogenates on the Motility, Oxygen Uptake and Fertilizing Capacity of Fowl Spermatozoa — Research Paper | ScholarLens