Reproduction   citetrack
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  

Journal of Reproduction and Fertility (1992) 96 699-707
DOI: 10.1530/jrf.0.0960699
Copyright © 1992 Society for Reproduction and Fertility
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nichol, R.
Right arrow Articles by Cooke, G. M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Nichol, R.
Right arrow Articles by Cooke, G. M.

Concentrations of energy substrates in oviductal fluid and blood plasma of pigs during the peri-ovulatory period

R. Nichol, R. H. F. Hunter, D. K. Gardner, H. J. Leese and G. M. Cooke

Summary. Large White gilts, 9 to 18 months old, that had exhibited at least two natural oestrous cycles were divided into three groups (phases): unmated pre-ovulatory, unmated post-ovulatory and mated post-ovulatory (n = 16, 20 and 18). Oviductal luminal fluid samples were collected under anaesthesia by micropipette from the ampulla and ampullary–isthmic junction and analysed by an ultramicrofluorometric technique. Glucose concentrations (mmol l–1, means combining regions; mean ± SEM) were significantly higher in blood plasma than in oviductal fluid (4·56 ± 0·20 versus 0·59 ± 0·16; P < 0·0001; n = 27), whereas lactate was higher in the oviduct (5·71 ± 0·53 versus 2·48 0·24; P < 0·0001; n = 27). No significant differences were found between the ampulla and the ampullary–isthmic junction. However, the concentration of glucose was significantly higher (P < 0·05) in the ampulla of the pre-ovulatory group (0·97 ± 0·20; n = 13) compared with the mated group (0·25 ± 0·05; n = 14) and its concentration in the ampullary–isthmic junction in the pre-ovulatory group (1·65 ± 0·63; n = 13) was significantly greater (P < 0·05) than in the post-ovulatory (0·43 ± 0·11; n = 11) or mated groups (0·17 ± 0·02; n = 14). Lactate in the ampulla of mated animals was higher than in the pre-ovulatory group (6·83 ± 0·70 versus 3·86 ± 0·38; P < 0·05; n = 15 and 13), but neither was significantly different from the post-ovulatory group. Furthermore, no change was seen at the ampullary–isthmic junction in lactate concentration with phase. Pyruvate concentrations showed no differences with phase, region or with plasma (oviduct 0·21 ± 0·02; plasma 0·14 ± 0·01; n = 27 and 26). Glucose concentration within the oviduct decreased at a time when gametes or embryos, with their liberated cumulus cells, were present. Consequently it is evident that the microenvironment of the gametes and embryos is changing and, in the light of these measurements, the composition of the media used for in vitro culture experiments may require modification to reflect the physiological levels more closely.

Keywords: oviductal fluid; pig; energy substrates; early development




This article has been cited by other articles:


Home page
Hum Reprod UpdateHome page
S. S. Suarez
Control of hyperactivation in sperm
Hum. Reprod. Update, November 1, 2008; 14(6): 647 - 657.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
P. J Booth, P. G Humpherson, T. J Watson, and H. J Leese
Amino acid depletion and appearance during porcine preimplantation embryo development in vitro
Reproduction, November 1, 2005; 130(5): 655 - 668.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
C. Mukai and M. Okuno
Glycolysis Plays a Major Role for Adenosine Triphosphate Supplementation in Mouse Sperm Flagellar Movement
Biol Reprod, August 1, 2004; 71(2): 540 - 547.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
R.H.F. Hunter
Tubal ectopic pregnancy: a patho-physiological explanation involving endometriosis
Hum. Reprod., July 1, 2002; 17(7): 1688 - 1691.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
K. Yoshioka, C. Suzuki, A. Tanaka, I. M.-K. Anas, and S. Iwamura
Birth of Piglets Derived from Porcine Zygotes Cultured in a Chemically Defined Medium
Biol Reprod, January 1, 2002; 66(1): 112 - 119.
[Abstract] [Full Text]


Home page
Biol. Reprod.Home page
T. E. Ludwig, J. M. Squirrell, A. C. Palmenberg, and B. D. Bavister
Relationship Between Development, Metabolism, and Mitochondrial Organization in 2-Cell Hamster Embryos in the Presence of Low Levels of Phosphate
Biol Reprod, December 1, 2001; 65(6): 1648 - 1654.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
T. E. Ludwig, M. Lane, and B. D. Bavister
Differential Effect of Hexoses on Hamster Embryo Development in Culture
Biol Reprod, May 1, 2001; 64(5): 1366 - 1374.
[Abstract] [Full Text]


Home page
Hum ReprodHome page
A.P. Gandhi, M. Lane, D.K. Gardner, and R.L. Krisher
A single medium supports development of bovine embryos throughout maturation, fertilization and culture
Hum. Reprod., February 1, 2000; 15(2): 395 - 401.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  
Copyright © 1992 by the Society for Reproduction and Fertility.