Page 271 - Anatomy and Physiology of Farm Animals, 8th Edition
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256 / Anatomy and Physiology of Farm Animals

                                                     Cells within target organs are capable of
          the cyclooxygenase (COX) enzyme fam-    recognizing and responding to a given
  VetBooks.ir  ily and it is important to remember that     hormone because they contain specific
          the  same enzymes that  are  involved
                                                  receptors capable of binding, or forming a
          in  the synthesis pathways for prosta-
          glandins are also used to synthesize    chemical union, with the hormone. As
          thromboxanes. Therefore, the side       described in Chapter  2, these cellular
          effects of these drugs (e.g., gastric ulcer-  receptors may be components of the cell
          ation and kidney injury) may occur due   membrane and have a binding site exposed
          to the indiscriminate inhibition of both   to the extracellular fluid, or they may be
          undesirable effects (i.e., inflammation)   contained within the cytoplasm or nucleus
          and important desirable effects (e.g.,   of cells. In either case, a receptor for a spe­
          maintenance  of  blood  flow  to  stomach   cific hormone must be present for a cell to
          and  kidneys).  NSAID  use  in  animals,   respond to the hormone and the sensitivity
          including injectable or oral Banamine®   of that cell to the hormone increases as
          (flunixin meglumine) and phenylbuta-    the number of available receptors for the
          zone, requires veterinary prescription     hormone increases in the cell.
          because of the additional consideration    The presence and number of receptors
          of withdrawal periods prior to slaughter   within target cells may change in certain
          and species specificity in dosing and   conditions. Such changes are one way that
          use; whereas aspirin and ibuprofen are   the biologic effect of a given hormone can
          over‐the‐counter NSAIDs widely used     be regulated. For example, levels of estro-
          by humans. Some newer NSAIDs have       gen, a reproductive hormone produced by
          been developed to selectively inhibit   the ovary prior to ovulation as well as by
          only certain enzymatic pathways to stop   the placenta during pregnancy, increases
          the production of prostaglandins associ-  in circulation shortly before birth (parturi­
          ated with inflammation (COX‐2) rather   tion). The increase in estrogen stimulates
          than those that are more protective and   an increase of  oxytocin receptors in the
          associated with activating platelets or   smooth muscle of the uterus. The increase
          protecting  the   stomach   (COX‐1).    in oxytocin receptors prepares the uterus
          Aspirin is particularly effective at inhib-  so that oxytocin can promote uterine con­
          iting the synthesis of thromboxanes for   tractions that are essential during parturi­
          blood clotting, and this is part of the   tion. Without the increase in oxytocin
          rationale for low‐dose aspirin use in   receptors stimulated by estrogen, oxytocin
          people to reduce the potential for clot   release itself would not provide adequate
          formation.                              uterine contractions for normal parturi­
                                                  tion. An increase in receptors on target
                                                  cells is termed  up‐regulation, and a
          Hormone Receptors                       decrease is termed down‐regulation.


          Only  certain specific populations  of  cells
          respond to an individual hormone. The   Cellular Effects of Peptide
          term target organ is used to identify the   Hormones
          tissue whose cells will be affected by a
          given hormone. Some hormones have       The receptors for peptide hormones are
          multiple target organs, for they affect cells   found in the cell membrane. Peptides can­
          in several sites. For example, both skeletal   not freely diffuse through the lipid bilayer
          muscle and liver are among the target   of the cell membrane, so their receptors
          organs for insulin. Table  13‐1 lists the   must be in the outer cell membrane to be
          major endocrine glands, their hormones,   available to the hormones in the extracel­
          and their general effects on their target   lular fluid. As described in Chapter  2,
          organs.                                 the  binding of the hormone with the
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