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Clinical Biochemistry of Domestic Animals (Sixth Edition) - UMK ...

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422<br />

Chapter | 14 Gastrointestinal Function<br />

TABLE 14-5 Gastrointestinal Peptide Hormones<br />

Hormone Source Action<br />

Gastrin G cells <strong>of</strong> pyloric antrum Gastric acid secretion<br />

Secretin S cells <strong>of</strong> duodenum and jejunum Pancreatic fluid and HCO 3<br />

<br />

secretion, bile secretion<br />

Cholecystokinin<br />

(pancreozymin)<br />

Somatostatin<br />

Enteroglucagon<br />

Gastric inhibitory<br />

polypeptide<br />

Duodenal and jejunal mucosa;<br />

myenteric plexus<br />

D cells <strong>of</strong> pancreas, CNS, gastric<br />

and intestinal mucosa<br />

L cells <strong>of</strong> small intestine, canine<br />

stomach<br />

Duodenal and jejunal mucosa<br />

Pancreatic enzyme secretion, gallbladder contraction, and<br />

sphincter <strong>of</strong> Oddi relaxation<br />

Inhibits effect <strong>of</strong> gastrin on gastric secretion, inhibits<br />

pancreatic enzyme secretion, stimulates ileal water and NaCl<br />

Control <strong>of</strong> intestinal cell growth<br />

Inhibits gastric secretion and stimulates intestinal secretion<br />

Motilin Upper small intestinal mucosa Stimulates gastrointestinal motility<br />

Stimulation <strong>of</strong> the vagus nerve causes a significant rise<br />

in pancreatic enzyme concentration. This type <strong>of</strong> response<br />

also is produced by cholecystokinin (pancreozymin), another<br />

polypeptide hormone produced by the duodenal mucosa,<br />

which also causes contraction <strong>of</strong> the gallbladder. The<br />

C-terminal pentapeptide <strong>of</strong> cholecystokinin-pancreozymin<br />

is exactly the same as that <strong>of</strong> gastrin. This fascinating relationship<br />

suggests that gastrin and cholecystokinin-pancreozymin<br />

participate in some integrated yet poorly understood<br />

system <strong>of</strong> digestive control.<br />

Several molecular forms <strong>of</strong> cholecystokinin (CCK)<br />

exist ( Ward and Washabau, 2005 ). CCK-33, CCK-39, and<br />

CCK-59 are the predominant forms that account for most<br />

<strong>of</strong> the gastrointestinal hormone responses. Endocrine cells<br />

in the duodenum and jejunum secrete CCK in response<br />

to intraduodenal fatty acids, amino acids, and H ion.<br />

CCK-8 is particularly important in cats. Intraluminal distension<br />

will activate CCK-8 containing neurons, resulting<br />

in acetylcholine release from the myenteric plexus and subsequent<br />

peristaltic reflexes in the ileum and colon. CCK-8<br />

neurons in the brain are involved in mediating the satiety<br />

response following eating.<br />

VI . OTHER GASTROINTESTINAL<br />

HORMONES<br />

A large number <strong>of</strong> polypeptides have been isolated from<br />

the gastrointestinal mucosa and have been classified as<br />

gut hormones ( Table 14-5 ). Some <strong>of</strong> these substances have<br />

not yet met all the rigid physiological requirements <strong>of</strong> true<br />

hormones. Some may have paracrine rather than endocrine<br />

activities—that is, their actions are on cells and tissues in<br />

the immediate vicinity <strong>of</strong> the cells <strong>of</strong> origin rather than<br />

being released into the vascular system.<br />

A . Motilin<br />

Motilin is a polypeptide containing 22 amino acids that<br />

was originally isolated from porcine duodenal mucosa<br />

( Brown et al., 1971 ). The amino acid composition and<br />

sequence have been described ( Brown et al., 1972, 1973 ).<br />

Immunoreactive motilin has been found in the enterochromaffin<br />

cells <strong>of</strong> the duodenum and jejunum <strong>of</strong> several<br />

species ( Polak et al., 1975 ), and, by means <strong>of</strong> radioimmunoassay,<br />

motilin has been identified in the plasma <strong>of</strong> dogs<br />

( Dryburgh and Brown, 1975 ). Motilin has been shown to<br />

stimulate pepsin output and motor activity <strong>of</strong> the stomach<br />

( Brown et al., 1971 ) and to induce lower esophageal<br />

sphincter contractions ( Jennewein et al., 1975 ). Studies by<br />

Itoh et al. (1978) suggest that motilin plays an important<br />

role in initiating interdigestive gastrointestinal contractions,<br />

which are referred to as the interdigestive motility<br />

complex or the migrating motility complex (MMC).<br />

The cyclic release <strong>of</strong> motilin from the intestinal mucosa<br />

coordinates gastric, pancreatic, and biliary secretions<br />

with phase III <strong>of</strong> the MMC ( Ward and Washabau, 2005 ).<br />

Erythromycin has been shown to induce an MMC similar<br />

to motilin and, along with other macrolide-like antibiotics,<br />

might be useful in selected cases with motility disorders.<br />

B . Somatostatin<br />

Somatostatin, which is named for its activity <strong>of</strong> inhibitory<br />

release <strong>of</strong> growth hormone from the pituitary gland, has<br />

been purified from ovine and bovine hypothalamus. The<br />

hypothalamic hormone is composed <strong>of</strong> 14 amino acids.<br />

Somatostatin also has been demonstrated in the stomach,<br />

pancreas, and intestinal mucosa in concentrations higher<br />

than in the brain ( Pearse et al., 1977 ). Somatostatin from<br />

porcine intestine has been isolated and sequenced, and it

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