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Effect of dietary lipids on fatty acid composition and fertility of fowl semen

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HAL Id: hal-00899967

https://hal.archives-ouvertes.fr/hal-00899967

Submitted on 1 Jan 1997

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Effect of dietary lipids on fatty acid composition and fertility of fowl semen

Elisabeth Blesbois, M Lessire, D Hermier

To cite this version:

Elisabeth Blesbois, M Lessire, D Hermier. Effect of dietary lipids on fatty acid composition and fertility of fowl semen. Reproduction Nutrition Development, EDP Sciences, 1997, 37 (3), pp.333-333.

�hal-00899967�

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Na-alginate, and for comparative pur-

poses, pectin were fed to faecal bacteria cul- tured in single-stage chemostats, with pH

control (6.5). Substrate (10 g.L- 1 ) was sup-

plied for 15 days, and samples were taken

for determinations of (3-eliminated products,

bacterial counts, isolation of alginate-degrad- ing populations, and measurements of

polyuronate depolymerase activities in bac- terial cell extracts.

(3-eliminated products accumulated in

alginate chemostats during the initial 4 days

of culture enrichment. Pectine decreased Fusobacterium sp populations whereas algi-

nate selected for aerobes microorganisms.

Bifidobacterial numbers were increased by alginate and decreased by pectine, however,

these effects were not significant.

All alginolytic bacteria isolated among anaerobes catalysed (3-elimination reactions.

Bacteria from both cultures exhibited low

pectin lyase activities (ca 0.5 !imol-p-elim- inated-products mg-protein- 1 ). Conversely, high alginate lyase activity (ca 9 !tmol-p-

eliminated-products mg-protein- 1 ) was

specifically detected in alginate chemostats, although it was not present on the first day

of culture. Hydrolase activity was high in pectin chemostats (ca 20 pmol-reducing-

ends mg-protein- 1 ), whereas reducing ends produced by cell extracts from alginate con- taining media corresponded only to bacterial lyase activities.

It is therefore concluded that alginate fer-

mentation by human intestinal bacteria first

requires substrate depolymerisation via (3-

elimination. Induction of alginate lyase

and/or enrichment in alginate degrading bac-

terial populations may explain the latency phase observed prior to fermentation. Bac- terial metabolism of (3-eliminated products

could also explain the lack of correlation between alginate utilization and SCFA for- mation.

Effect of dietary lipids on fatty acid com- position and fertility of fowl semen. E E

Blesbois M Lessire D Hermier (Inra, sta-

tion de recherches avicoles, 37380 Nouzilly, France). ).

Phospholipids are the major lipids (- 80%) of spermatozoa (SPZ) and contain -30% of n-6 polyunsaturated fatty acids (FA). The role of these FA on fertility has been inves-

tigated in 32 male fowls receiving isolipidic

diets containing 5% of either salmon oil

(salmon, n-6/n-3

=

1.1 ) or corn oil (corn, n-6/n-3 = 41.6). Analyses were performed

on composition of spermatozoa (SPZ) and of

seminal plasma (SP) and on fertilizing abil- ity after artificial insemination. SP contained

more saturated FA than SPZ, respectively

50% and 40%. SP and SPZ had high

amounts of 20:4 n-6 (5-9%) and 22:4 n-6 ( 11-21 %); these two FA were absent from the diets and partly replaced 18:2 n-6 in sperm (only 2-6% in sperm vs 15!6% in the diets). Moreover, when compared to the

corn diet, the salmon diet increased signif- icantly the amount of n-3 long-chain FA (6.7% vs 2.6%) and decreased the amount of n-6 long-chain FA (23.3% vs 33.3%). In parallel, the fertility rate was significantly higher with the salmon diet (96.0% vs

91.5% with the com diet). Thus the nature of dietary FA may influence the fertilizing abil- ity of fowl semen, probably by modifying

the n-6/n-3 ratio of membrane lipids.

Additive effect of A→G (-3826) variant of the uncoupling protein gene and the

Trp64Arg mutation of the β3-adrenergic

receptor gene on weight gain in morbid obesity. K K Clément Clément 1,2 , J Ruiz J Ruiz 2,4 , AM AM Cas- Cas- sard-Doulcier F Bouillaud D Ricquier 3

A Basdevant B Guy-Grand P Froguel (

1 Département de nutrition, Hôtel-Dieu, 75004 Paris; 2 CNRS EP 10, Institut Pas- teur de Lille, 59000 Lille; 3 CNRS, 92000 Meudon, France; 4 Division d’endocrinolo-

gie et métabolisme, Lausanne, Switzerland).

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