Page 55 - Small Animal Clinical Nutrition 5th Edition
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Macronutrients         55



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                  Figure 5-6. Schematic of how total gross energy of a food is partitioned into digestible energy, metabolizable energy and net energy. Net
                  energy can be further partitioned into energy used for maintenance (NE ) and production (NE ).
                                                                                     p
                                                                     m
                  Acetyl-CoA is then oxidized in the TCA cycle and ATP is  needs energy, it uses glycogen first, fat stores second and final-
                  generated via oxidative phosphorylation in the electron trans-  ly, as a last resort, amino acids from body protein (Chapter 25).
                  port chain. The number of ATP generated from fatty acid oxi-  In fed animals, food energy is primarily used for meeting body
                  dation depends on the length of the carbon chain and degree of  energy needs, thus preserving body tissues by preventing catab-
                  unsaturation. For example, myristic acid (C14:0) yields 112  olism. Further discussions of use and control of body energy
                  ATP, palmitic acid (C16:0) 129 ATP, palmitoleic acid (C16:1)  stores during exercise can be found in Chapter 18.
                  127 ATP, stearic acid (C18:0) 146 ATP and oleic acid (C18:1)  Differences in the amount of energy consumed and that
                  144 ATP.                                            expended by the body can clearly result in changes in body
                    Amino acids obtained from the diet and generated by  weight, growth rate and body composition (especially body fat).
                  endogenous protein breakdown are (re)used for protein syn-  Excess energy intake and storage relative to energy expenditure
                  thesis or oxidized as an energy source. Protein synthesis  is a common problem in pet dogs and cats (e.g., obesity). Obese
                  requires a substantial expenditure of energy. When amino  pets are at increased risk for developing a variety of health prob-
                  acids are oxidized, there are additional energy costs associated  lems (Chapter 27). Excess energy intake in growing large- and
                  with gluconeogenesis and ureagenesis (Flatt, 2001). As a  giant-breed puppies may be related to developmental skeletal
                  result the efficiency to derive energy from protein is consider-  abnormalities (Chapter 33). Conversely, inadequate energy
                  ably less than that from fat or carbohydrate. The amino acids  intake relative to expenditure may occur in animals with cancer
                  used for energy are deaminated or transaminated to yield a  and heart disease and resulting in cachexia (Chapters 30 and
                  carbohydrate moiety and ammonia; the ammonia is then con-  36) and in vigorously exercising dogs such as sled dogs
                  verted to urea. The carbon skeleton enters the TCA cycle and  (Chapter 18).
                  ATP is formed in the electron transport chain. The number
                  of ATP generated from oxidation of amino acids to water,  Energy Analyses
                  carbon dioxide and urea varies, but ranges from six ATP from  The most accurate determination of the DE or ME content of
                  glycine to 42 ATP from tryptophan.                  food (Figure 5-6) is obtained through feeding studies (Yamka
                                                                      et al, 2007; McDonald et al, 1995; AAFCO, 2007). ME deter-
                  Energy Storage                                      minations involve the direct measurement of energy intake and
                  ATP is the usable form of energy for body cells, but not a good  energy lost in feces and urine obtained from digestion or
                  energy storage molecule because it is used quickly after forma-  metabolism studies.Energy lost as expired gases (e.g.,methane)
                  tion. Glycogen and triglycerides are better storage forms of  is negligible (McKay and Eastwood, 1984). As a result, energy
                  energy. Production and use of ATP are equally balanced  lost as gases is typically ignored when calculating ME for dogs
                  through a series of control mechanisms that monitor the  and cats. The Association of American Feed Control Officials
                  amount of ATP available. After a meal containing adequate  (AAFCO) has published accepted protocols for the determina-
                  energy, the total body metabolism is generally anabolic; the  tion of ME of dogs and cat foods (2007) (Box 5-3). Because of
                  body uses energy for synthetic reactions and tissue accretion  the laborious nature of determining the actual ME content of
                  (e.g., growth, reproduction). After the body has enough energy  dog foods, calculated ME values are used extensively for diet
                  to meet demands, the pathways of glycolysis, β-oxidation,  formulation and food labeling (Yamka et al, 2007).
                  transamination, deamination and the TCA cycle are slowed.  Currently, AAFCO (2007) and the National Research
                  The pathways of glycogen and fat synthesis are simultaneously  Council (2003) recommend a predictive equation largely based
                  accelerated and excess dietary energy is stored as glycogen and  on fixed energy values and digestibility coefficients for dietary
                  body fat.These energy stores can then be used to generate ATP  components (i.e., crude protein, crude fat and carbohydrate) for
                  later when needed.Generally,in fasting animals,when the body  estimating the ME content of dog foods. Although this predic-
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