26.12.2014 Views

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

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

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

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

X. Exocrine Pancreatic Disease<br />

863<br />

Spontaneous diabetes mellitus, as characterized by polyuria/polydipsia<br />

(PU/PD), glucosuria, persistent hyperglycemia,<br />

and loss <strong>of</strong> weight despite good appetite, has been<br />

reported in a number <strong>of</strong> avian species, including budgerigars,<br />

cockatiels, an Amazon parrot, an African grey parrot,<br />

toco toucans, a red-tailed hawk, and the pigeon ( Altman<br />

and Kirmayer 1976 ; Candeletta et al ., 1993 ; Lothrop et al .,<br />

1986 ; Lumeij 1994c ; Murphey, 1992b ; Schlumberger 1956 ;<br />

Spira, 1981 ; Wallner-Pendleton et al ., 1993 ; Wiesner, 1971 ;<br />

Woerpel et al ., 1987 ).<br />

The species that will be most commonly encountered<br />

in clinical avian practice are budgerigars, cockatiels, and<br />

toco toucans. A tentative diagnosis can be made by finding<br />

glucose in the urine using a test strip (Testape, Eli-Lilly<br />

Benelux NV, Amsterdam), whereas a definitive diagnosis<br />

can be made by finding an elevated plasma glucose concentration.<br />

PU/PD accompanied by glucosuria does not<br />

always indicate diabetes mellitus. Diabetes mellitus can<br />

only be diagnosed if elevated plasma glucose concentrations<br />

have been demonstrated.<br />

In mammals, Fanconi’s syndrome is known, characterized<br />

by renal glucosuria, hyperaminoaciduria, and<br />

hyperphosphaturia, as well as renal loss <strong>of</strong> potassium,<br />

bicarbonate and water, and other substances conserved by<br />

the proximal tubule. Fanconi’s syndrome should be considered<br />

as the final result <strong>of</strong> any one <strong>of</strong> many possible primary<br />

insults to proximal tubular function. The patient’s symptoms<br />

reflect the disturbance <strong>of</strong> tubular function, in addition<br />

to the primary cause <strong>of</strong> the syndrome. The syndrome may<br />

be inherited or acquired.<br />

There are some striking differences between birds and<br />

mammals with regard to pancreatic control <strong>of</strong> carbohydrate<br />

metabolism. In mammals, pancreatectomy results in diabetes<br />

mellitus. Reported effects <strong>of</strong> pancreatectomy in birds<br />

are controversial. However, the more recent experiments<br />

performed on granivorous birds indicate that surgical extirpation<br />

or destruction <strong>of</strong> the pancreas with cytotoxic agents<br />

leads to hypoglycemic crisis and death. The few reported<br />

pancreatectomies performed on carnivorous birds have<br />

always led to diabetes mellitus. It is generally accepted<br />

that glucagon is more effective in granivorous birds, which<br />

exhibit a marked insulin insensitivity. The limited data<br />

available on spontaneous diabetes mellitus in granivorous<br />

birds suggest that in these species diabetes mellitus is not<br />

caused by an insulin deficiency. Birds <strong>of</strong> prey may be<br />

much more insulin dependent.<br />

Spontaneous diabetes mellitus in birds has been<br />

reported to be successfully treated with daily injections <strong>of</strong><br />

insulin in dosages comparable to doses used in dogs. These<br />

successful treatments <strong>of</strong> diabetic birds (disappearance <strong>of</strong><br />

clinical signs) are surprising, considering the relative insulin<br />

insensitivity that has been reported to occur in a variety<br />

<strong>of</strong> avian species.<br />

Plasma insulin and glucagon concentrations have been<br />

established in three birds with hyperglycemia ( Lothrop<br />

et al ., 1986 ). In all cases, insulin concentrations were similar<br />

to those <strong>of</strong> controls, whereas glucagon concentrations, on<br />

the other hand, were extremely high or extremely low. In<br />

another case <strong>of</strong> diabetes mellitus (DM) in an African grey<br />

parrot, Candeletta et al. (1993) reported extremely low<br />

insulin concentrations. It is not clear whether these determinations<br />

were accurate. The findings, however, suggest<br />

that different etiologies were likely to be involved.<br />

Speculations on possible etiologies <strong>of</strong> diabetes mellitus<br />

in birds have been discussed ( Lumeij, 1994c ).<br />

X . EXOCRINE PANCREATIC DISEASE<br />

Exocrine pancreatic hormones that are present in the duodenum<br />

<strong>of</strong> birds include amylase, lipase, trypsin, and chymotrypsin.<br />

They facilitate degradation <strong>of</strong> carbohydrates,<br />

fats, and proteins, respectively. The inactive precursors <strong>of</strong><br />

trypsin and chymotrypsin, trypsinogen, and chymotrypsinogen<br />

enter the duodenum, where they are activated by<br />

intestinal enterokinase. This mechanism prevents autodigestion<br />

<strong>of</strong> pancreatic tissue ( Duke, 1986 ).<br />

There are two basic manifestations <strong>of</strong> exocrine pancreatic<br />

hormone disorders: (1) acute pancreatitis or acute pancreatic<br />

necrosis, and (2) chronic pancreatitis resulting in<br />

pancreatic fibrosis and pancreatic exocrine insufficiency.<br />

The pathogenesis <strong>of</strong> acute pancreatitis involves the activation<br />

<strong>of</strong> pancreatic enzymes in and around the pancreas<br />

and bloodstream, resulting in coagulation necrosis <strong>of</strong> the<br />

pancreas and necrosis and hemorrhage <strong>of</strong> peripancreatic<br />

and peritoneal adipose tissue. Increased amylase and lipase<br />

activities in plasma have been reported from birds with<br />

active pancreatitis.<br />

Reference values for plasma lipase and amylase have<br />

been established in a population <strong>of</strong> 87 African grey parrots<br />

(Van der Horst and Lumeij, unpublished observations).<br />

α -Amylase activity in plasma was determined with a kinetic<br />

p -nitrophenylmaltoheptaoside method (Sopachem α-Amylase<br />

kit # 003-0311-00 Sopar-biochem, 1080 Brussels) at 30°C.<br />

Values ranged from 571 to 1987 U/L (inner limits <strong>of</strong> P 2.5 to<br />

P 97.5 with a probability <strong>of</strong> 90%).<br />

Lipase activity was measured at 30° C using a test based<br />

on the conversion <strong>of</strong> triolein by lipase to monoglyceride<br />

and oleic acid. The associated decreased turbidity was<br />

measured in the UV range (Boehringer Mannheim kit #<br />

MPR 3-1442651). Reference values ranged from 268 to<br />

1161 U/L.<br />

Hochleithner (1989b) reported reference values for<br />

plasma amylase in four different psittacine species using<br />

a dry chemistry system (Kodak Ektachem, Amylopectin,<br />

25°C; Kodak Company, 1986 ). The values were considerably<br />

lower as compared to the ones just discussed: budgerigar<br />

( n 50) 187 to 585 U/L, African grey parrot ( n 68 )<br />

211 to 519 U/L, Amazon parrot ( n 30) 106 to 524 U/L,<br />

and macaw 276 to 594 U/L.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!