Page 334 - Small Animal Clinical Nutrition 5th Edition
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Feeding Working and Sporting Dogs   341


                  fit to racing dogs, particularly if they are fed raw meat. Rapid  replaced through dietary intake.
        VetBooks.ir  fermentation of oligosaccharides may decrease colonic pH  even greater in underfed athletes and those participating in
                                                                        The proportion of energy supplied by amino acids may be
                  and inhibit clostridial growth (Amtsbert et al, 1989). Fructo-
                                                                      ultra-endurance events in which there is a high risk for deple-
                  oligosaccharides inhibit cecal colonization by Salmonella
                  species in chickens and could conceivably do so in dogs (Baily  tion of endogenous carbohydrate stores (Zackin, 1990; Miller
                  et al, 1991).                                       and Massaro, 1989). In these instances, gluconeogenesis
                                                                      becomes the major pathway for maintaining blood glucose lev-
                  Protein                                             els (Zackin, 1990; Miller and Massaro, 1989). Because amino
                  Dietary protein is used to fulfill structural, biochemical and, to  acids are the predominant substrate used by the gluconeogenic
                  a lesser extent, energy requirements. Work increases the  pathway, their rate of catabolism is increased whenever this
                  requirement for protein.The magnitude of this increase and the  pathway is accelerated (Hickson and Wolinsky, 1989; Cahill et
                  best strategy for meeting it are subjects of much debate in  al, 1970).
                  canine performance nutrition.                         This concept raises an important point: it is disadvantageous
                    The work-induced elevation in protein requirement is most  for an athlete to rely heavily on endogenous sources of protein
                  pronounced when the intensity and/or duration of exercise per-  for energy. There are no known labile stores of protein in the
                  formed is rapidly increased above an animal’s present level of  canine body. All protein sources serve a structural or functional
                  conditioning.These circumstances are encountered at the onset  purpose (Cahill et al, 1970). Interestingly, skeletal muscle is
                  of a training program, when the duration or intensity of train-  readily mobilized. Overuse of this source would have an obvi-
                  ing bouts is increased and especially during performances  ous negative impact on performance. Because the small pool of
                  (Zackin, 1990; Hickson and  Wolinsky, 1989). A common  circulating amino acids is insufficient to meet the amino acid
                  example would be when a bird dog that is also a minimally  requirements of the anabolic and catabolic processes described
                  active pet is hunted the first time during hunting season with  above, dietary protein intake must supply the deficit if nitrogen
                  little or no exercise training. The increase in protein demand is  balance is to be maintained (Zackin, 1990).
                  due to combined increases in the rates of tissue protein synthe-  For endurance athletes, there may be some disadvantages
                  sis and catabolism.                                 inherent to exploiting dietary protein sources for energy.
                    Several anabolic processes contribute to the exercise-  Protein has only about 3.5 kcal (15 kJ) ME/g DM. Thus,
                  induced increment in protein requirement. Protein demand is  increasing the proportion of protein in the formulation cannot
                  elevated due to an increase in the synthesis of structural and  increase the energy density of a ration. The energy density of
                  functional proteins. Training induces synthesis of many  the food is one of the major determinants of endurance capac-
                  enzymes and transport proteins in each of the energy-gener-  ity when working dogs have difficulty ingesting as many kcal as
                  ating pathways (Nadel, 1985; Williams, 1985; Costill et al,  they expend (Downey et al, 1980).
                  1979, 1979a). Blood volume also expands during aerobic  Excessive protein intake may predispose an animal to
                  training (Nadel, 1985; Williams, 1985; Zackin, 1990;  increased amino acid catabolism because dietary amino acids
                  Hickson and Wolinsky, 1989). Such expansion necessitates an  are not stored in labile protein depots, but are deaminated
                  increase in plasma protein synthesis to maintain oncotic and  (Hickson and  Wolinsky, 1989). The resulting ketoacids are
                  osmotic balance between plasma and interstitial fluids  either oxidized for energy directly or converted into fatty acids
                  (Pivarnik, 1994). The increase in hematocrit sometimes  and/or glucose and then stored as adipose tissue or glycogen.
                  observed during endurance conditioning programs may  The urea produced from amino acid breakdown is excreted
                  reflect an increase in tissue protein synthesis (Nadel, 1985;  from the body in urine. In healthy animals, the amount of water
                  Williams, 1985; Kronfeld and Downey, 1981). Anaerobic  lost increases with increased urea production.
                  training regimens may also induce muscle hypertrophy  An optimal food for a working or sporting dog should con-
                  (Hickson and Wolinsky, 1989). Amino acids are used in the  tain enough high-quality protein to meet the dog’s anabolic
                  formation of new muscle tissue and in the repair of damage  requirements and enough non-protein energy nutrients to
                  that may occur to muscle and connective tissue during inten-  meet its energy requirements. Such a food encourages the use
                  sive conditioning programs. In addition to enhancing the rate  of ingested protein in synthetic rather than energy-generating
                  of tissue protein synthesis, exercise increases the rate of amino  processes. As non-protein caloric intake increases, less dietary
                  acid catabolism. Amino acids may provide between 5 and 15%  protein is used for energy and more is available for use in ana-
                  of the energy used during exercise, depending on the intensi-  bolic processes. Energy requirements should be met by fat and
                  ty and duration of the task (Young et al, 1962; Zackin, 1990;  carbohydrate, leaving the majority of amino acids available for
                  Hickson and  Wolinsky, 1989). Most of this energy comes  synthetic purposes. During long-duration exercise, DER may
                  from the oxidation of branched-chain amino acids (Miller  increase several-fold whereas protein requirement increases
                  and Massaro, 1989; Blomstrand et al, 1988). All three amino  only a few percent. To meet the energy needs of hard-work-
                  acids belonging to this group (leucine, isoleucine, valine) are  ing dogs, either more food must be consumed (increasing
                  “essential” and thus cannot be synthesized from other amino  both energy and protein intake equally) or a higher energy,
                  acids in sufficient quantities to meet requirements. The  lower protein food must be fed (increasing energy intake more
                  branched-chain amino acids lost through exercise must be  than protein intake). Providing sufficient dietary energy by
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