» Articles » PMID: 12743722

Changes in Tissue Fatty Acid Composition During the First Month of Growth of the King Penguin Chick

Overview
Date 2003 May 14
PMID 12743722
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

The switch from yolk to food (myctophid fishes) as the nutrient source for the newly hatched chick of the king penguin ( Aptenodytes patagonicus) results in a profound change in the pattern of fatty acid provision. This is characterized by major increases in the proportionate intake of n-3 polyunsaturates (20:5n-3 and 22:6n-3) and long chain (C(20-24)) monounsaturates, accompanied by relatively lower levels of n-6 polyunsaturates (18:2n-6 and 20:4n-6). The effects of this change on the fatty acid composition of tissue lipids during the first month of growth, a period of tissue maturation leading to thermal emancipation, were determined. The composition of adipose tissue triacylglycerol responded rapidly to the switch in nutrient source, the proportion of long chain monounsaturates (mainly 20:1n-9 and 22:1n-11) increasing five-fold between hatch and emancipation while the relative levels of 20:5n-3 and 22:6n-3 also increased significantly, by 3- and 1.2-fold, respectively. At emancipation, the fatty acid profile of adipose tissue triacylglycerol was essentially identical to that of the diet. At hatch, the main polyunsaturates of muscle phospholipid were 20:4n-6, 20:5n-3, and 22:6n-3, respectively, forming (w/w of fatty acids) 13.2%, 5.0%, and 12.0%. By emancipation, 20:4n-6 had decreased to 4.8%, 20:5n-3 increased to 10.9%, and 22:6n-3 at 11.4% showed little change. The main polyunsaturate in brain phospholipid at hatch was 22:6n-3 (19.3%): this remained almost constant until day 15 but then increased significantly to 23.6% by emancipation. Significant but minor changes in the proportions of 20:4n-6 (from 5.2% at hatch to 3.5% at emancipation) and 20:5n-3 (from 3.0% to 3.9%) were also observed in brain phospholipid. The data do not allow us to completely distinguish changes that are solely diet driven from those which are a consequence of tissue differentiation. Nevertheless, it is evident that, whereas the fatty acid composition of adipose tissue responds faithfully to the change in nutrient source, the phospholipids of muscle and, especially, of brain are much more refractory to the effects of diet during this period of tissue maturation.

Citing Articles

Short-term dietary changes are reflected in the cerebral content of adult ring-billed gulls.

Lamarre J, Wilson D R Soc Open Sci. 2024; 11(8):240616.

PMID: 39113770 PMC: 11303033. DOI: 10.1098/rsos.240616.


Omega-3 fatty acids accelerate fledging in an avian marine predator: a potential role of cognition.

Lamarre J, Cheema S, Robertson G, Wilson D J Exp Biol. 2021; 224(Pt 4).

PMID: 33462136 PMC: 7929930. DOI: 10.1242/jeb.235929.


Development of endothermy in birds: patterns and mechanisms.

Price E, Dzialowski E J Comp Physiol B. 2017; 188(3):373-391.

PMID: 29119278 DOI: 10.1007/s00360-017-1135-0.


Effect of species and genotype on the efficiency of enrichment of poultry meat with n-3 polyunsaturated fatty acids.

Rymer C, Givens D Lipids. 2006; 41(5):445-51.

PMID: 16933789 DOI: 10.1007/s11745-006-5118-2.

References
1.
Salem Jr N, Litman B, Kim H, Gawrisch K . Mechanisms of action of docosahexaenoic acid in the nervous system. Lipids. 2001; 36(9):945-59. DOI: 10.1007/s11745-001-0805-6. View

2.
Surai P, Sparks N . Tissue-specific fatty acid and alpha-tocopherol profiles in male chickens depending on dietary tuna oil and vitamin E provision. Poult Sci. 2000; 79(8):1132-42. DOI: 10.1093/ps/79.8.1132. View

3.
Katsuki H, Okuda S . Arachidonic acid as a neurotoxic and neurotrophic substance. Prog Neurobiol. 1995; 46(6):607-36. DOI: 10.1016/0301-0082(95)00016-o. View

4.
Decrock F, GROSCOLAS R, McCartney R, Speake B . Transfer of n-3 and n-6 polyunsaturated fatty acids from yolk to embryo during development of the king penguin. Am J Physiol Regul Integr Comp Physiol. 2001; 280(3):R843-53. DOI: 10.1152/ajpregu.2001.280.3.R843. View

5.
Ayre K, Hulbert A . Effects of changes in dietary fatty acids on isolated skeletal muscle functions in rats. J Appl Physiol (1985). 1996; 80(2):464-71. DOI: 10.1152/jappl.1996.80.2.464. View