Whole-body urea cycling and protein turnover during hyperphagia and dormancy in growing bears (Ursus americanus and U-arctos)

被引:97
作者
Barboza, PS
Farley, SD
Robbins, CT
机构
[1] Smithsonian Inst, Natl Zool Pk, Washington, DC 20008 USA
[2] Washington State Univ, Dept Nat Resource Sci, Pullman, WA 99164 USA
关键词
D O I
10.1139/z97-848
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Subadult bears were studied during their autumn hyperphagia (n = 3) and winter dormancy (n = 6). Urea kinetics were measured with C-14- and N-15-urea, protein turnover was estimated with N-15-glycine, and body composition was assessed with H-3-water. Reduced amino acid degradation in winter was indicated by declines in plasma urea and aminotransferase activities, and lower urea production than in autumn (4.7 vs. 27.5 mmol urea-N.kg(-0.75).d(-1)). Only 7.5% of urea produced in hyperphagic bears was degraded and just 1.1% of the degraded N reutilized as amino-N. Dormant bears reutilized 99.7% of urea produced, indicating thorough microbial ureolysis and urea-N resorption. Low rates of body N loss during dormancy suggested losses of non-urea N as creatinine. Protein turnover rates (15.2-21.5 g.kg(-0.75).d(-1)) were similar between seasons and reflected the apparent maintenance of hepatic, intestinal, and muscular functions through dormancy. Protein synthesis accounted for 32% of energy expended in dormancy, which was mainly (91.5%) derived from fat oxidation. Consistent organ function and body temperature in dormant bears enables recycling of urea-N, which minimizes body protein loss and conserves mobility. In comparison with heterothermic hibernation, ursid dormancy would provide greater flexibility during winter and facilitate rapid resumption of foraging and growth in spring.
引用
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页码:2129 / 2136
页数:8
相关论文
共 62 条
[1]  
ADAMS SH, 1993, J COMP PHYSIOL B, V163, P367
[2]  
AHLQUIST DA, 1976, PHYSIOLOGIST, V19, P107
[3]   FUNCTIONAL ROLES OF UREA SYNTHESIS IN VERTEBRATES [J].
ATKINSON, DE .
PHYSIOLOGICAL ZOOLOGY, 1992, 65 (02) :243-267
[4]   Changes in the body composition of fasting polar bears (Ursus maritimus): The effect of relative fatness on protein conservation [J].
Atkinson, SN ;
Nelson, RA ;
Ramsay, MA .
PHYSIOLOGICAL ZOOLOGY, 1996, 69 (02) :304-316
[5]   POSSIBLE MECHANISMS RESPONSIBLE FOR THE REDUCED INTESTINAL FLORA IN HIBERNATING LEOPARD FROGS (RANA-PIPIENS) [J].
BANAS, JA ;
LOESCHE, WJ ;
NACE, GW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1988, 54 (09) :2311-2317
[6]   NITROGEN-METABOLISM AND REQUIREMENTS OF NITROGEN AND ENERGY IN THE WOMBATS (MARSUPIALIA, VOMBATIDAE) [J].
BARBOZA, PS ;
HUME, ID ;
NOLAN, JV .
PHYSIOLOGICAL ZOOLOGY, 1993, 66 (05) :807-828
[7]   THE METABOLISM OF [UREA-C-14 BY CONTROL AND STARVED RICHARDSONS GROUND-SQUIRRELS [J].
BINTZ, GL ;
TORGERSON, GE .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 1981, 69 (03) :551-555
[8]  
Blaxter K., 1989, Energy metabolism in animals and man
[9]   RENAL FUNCTION IN ANESTHETIZED DORMANT AND ACTIVE BEARS [J].
BROWN, DC ;
MULHAUSEN, RO ;
ANDREW, DJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1971, 220 (01) :293-+
[10]   NUTRIENT RESERVE DYNAMICS AND ENERGETICS DURING LONG-TERM FASTING IN THE KING PENGUIN (APTENODYTES PATAGONICUS) [J].
CHEREL, Y ;
GILLES, J ;
HANDRICH, Y ;
LEMAHO, Y .
JOURNAL OF ZOOLOGY, 1994, 234 :1-12