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Feeding Working and Sporting Dogs   337


                  working and sporting dogs, depending on the type, level and  Table 18-10. Effect of nutrient profile on stamina.*
        VetBooks.ir  duration of physical activity.                    Nutrient (DM)    Food A    Food B    Food C

                  Fat
                  Fat provides approximately 8.5 kcal (36 kJ) of metabolizable  Energy density (kcal/g)  4.7  5.9  6.0
                                                                       Fat (%)           12.8      28.3       33.1
                  energy (ME) per gram of dry matter (DM) or more than twice  Protein (%)  22.9    48.7       30.5
                  the amount provided by protein and carbohydrate. Because of  Performance
                  these differences in caloric density, the only practical means of  Time (minutes)  103.7  136.1  137.6
                                                                       Distance (miles)  15.5      20.4       20.6
                  significantly increasing the energy density of a food is to  Key: DM = dry matter, Food A = grocery brand dry food, Food B =
                  increase its fat concentration. Reasonable increases in fat usual-  grocery brand moist food, Food C = specialty brand dry food.
                  ly also increase palatability. Energy density and palatability  *Adapted from: Downey RL, Kronfeld DS, Banta CA. Diet of bea-
                                                                       gles affects stamina. Journal of the American Animal Hospital
                  make dietary fat levels an important consideration in the for-  Association 1980; 6: 273-277.
                  mulation of foods for working and sporting dogs. Increasing
                  dietary fat generally also increases a food’s digestibility because
                  fat tends to be more digestible than protein or carbohydrate.  The effect of food on insulin levels has also been demonstrat-
                  Also, when a greater quantity of a lower energy density food is  ed in well-trained human athletes (Gleeson et al, 1986; Martin
                  eaten in an attempt to provide adequate calories, there is a more  et al, 1978; Coyle et al, 1985; Yoshida, 1986; Brouns et al,
                  rapid rate of passage through the gastrointestinal (GI) tract,  1989). People eating high-fat foods had significantly lower
                  further reducing digestibility and energy intake (Davenport et  resting insulin concentrations than those eating high-carbohy-
                  al, 2001).                                          drate foods (Maughan et al, 1987). Insulin decreases the release
                    Ingesting adequate calories to meet daily energy expenditure  of FFA from peripheral adipose stores through its inhibitory
                  is often a serious challenge for working dogs. In extreme cases,  effects on the activity of hormone-sensitive lipase. Dogs rely
                  sled dogs in long-distance races expend from 6,000 to 10,000  more heavily on FFA for energy generation at all exercise inten-
                  kcal/day (25 to 42 MJ/day), in which case DM intake becomes  sities than people do; therefore, the effect of food on resting
                  a performance-limiting factor. Because the total daily DM  insulin levels is a matter of even greater concern for working
                                                        c
                  intake is limited to about 3.5% of body weight, the energy  and sporting dogs (Reynolds et al, 1997). Increased dietary fat
                  density of a food should be maximized. Under these circum-  (from 25 to 65% of kcal) increases VO max and the maximal
                                                                                                    2
                  stances, each nonessential gram of protein and carbohydrate  rate of fat oxidation by 20 to 30% in well-trained dogs
                  ingested potentially robs the dog of 5 kcal (21 kJ). The calorie  (Reynolds et al, 1995). These increases were associated with a
                  deficit is paid through mobilization of body fat stores. Over-  25 to 30% increase in mitochondrial volume, possibly account-
                  reliance on these depots may lead to catabolism of more func-  ing for the increased oxidative capacity. Protein and total caloric
                  tionally crucial energy sources, such as muscle and plasma pro-  intake were identical between groups. Also, event anticipation
                  teins. In addition to its role as an energy store, adipose tissue  can suppress insulin concentrations before and during an event
                  also functions as an insulator. Excessive adipose depletion may  activity (Gillette et al, 2006).
                  increase a dog’s cost of maintaining its body temperature, espe-  The relationship between fat intake and canine endurance is
                  cially at rest in cold environments.                well established. The time to exhaustion for well-conditioned
                    Even under the less severe conditions of intermediate exer-  beagles running on a treadmill was directly related to energy
                  cise, increased dietary fat levels provide needed energy and  density, digestibility and digestible fat intake (Table 18-10)
                  other valuable benefits. Fatigue and dehydration may decrease  (Downey et al, 1980). Practical applications of this concept are
                  appetite. Increasing dietary fat concentration increases energy  evident in the performance foods currently fed to many suc-
                  intake and encourages stressed dogs to ingest more food  cessful working and sporting dogs. As the duration of the event
                  because the higher fat content improves palatability.  performed by a dog increases, so should the dietary fat intake.
                    Feeding high levels of fat can positively affect endurance.  Dogs can tolerate high levels of dietary fat if fat is gradually
                  Training may elevate the carbohydrate threshold, thus increas-  introduced and an adequate intake of non-fat nutrients is main-
                  ing the proportion of energy supplied by free fatty acid (FFA)  tained. Steatorrhea and a decrease in food palatability are indi-
                  oxidation at all but the highest intensities of exercise. Increasing  cators that the fat content of a food has exceeded a dog’s fat tol-
                  dietary fat concentration may augment this process by enhanc-  erance. Under conditions of extreme training, sled dogs may
                  ing FFA availability (Kronfeld and Downey, 1981; Kronfeld et  ingest up to 60% of their energy as fat. During ultra-endurance
                  al, 1977; Reynolds et al, 1994). Working dogs fed high-fat  events, such as the Iditarod or the Yukon Quest, fat intake may
                                                                                                   d
                  foods have higher circulating levels of FFA at rest and respond  compose 80% of the calories ingested. This “super fat loading”
                  to exercise stimuli by releasing more FFA than those fed  should be attempted only during the most strenuous periods of
                  isocaloric amounts of a high-carbohydrate food (Kronfeld and  such events, when it is difficult or impossible for dogs to ingest
                  Downey, 1981; Kronfeld et al, 1977; Young et al, 1962). This  as much energy as they are expending.
                  difference in FFA availability may be related to the decreased  Anemia has been associated with impaired performance in
                  resting plasma concentration of insulin in animals fed high-fat  dog teams fed very high-fat foods (i.e., 80% kcal from fat) for
                  foods, and the induction of key lipolytic enzymes.  prolonged periods (i.e., weeks to months) (Reynolds, 1997).
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