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

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858<br />

Chapter | 28 Avian <strong>Clinical</strong> <strong>Biochemistry</strong><br />

Bile acid (µmol/l)<br />

80<br />

60<br />

40<br />

20<br />

FIGURE 28-17 Plasma bile acid concentrations<br />

(mean SD) in peregrine falcons, Falco peregrinus<br />

(n 6) after a 42-h fasting period and 3, 8, 15, and 24 h<br />

after birds were fed a complete skinned quail, Coturnix<br />

coturnix, at 0 h. Values at 3, 8, and 15 h are significantly<br />

different from values at 0 and 24 h ( p 0.05). Reprinted<br />

with permission from Lumeij and Remple (1992 ).<br />

0<br />

0 5 10 15 20 25<br />

Time (hr)<br />

( Gracula religiosa ) and toucans ( Rhamphastos spp.). In these<br />

species, hemochromatosis is <strong>of</strong>ten associated with hepatic<br />

fibrosis, but the causal relation has not been confirmed.<br />

Hemosiderosis should be considered in the differential<br />

diagnosis <strong>of</strong> avian hepatopathy. Diagnostically, determination<br />

<strong>of</strong> blood iron concentrations is not reliable. There is,<br />

however, a positive correlation between the concentration<br />

<strong>of</strong> stainable iron determined by image analysis <strong>of</strong> histological<br />

sections and biochemically determined liver iron concentration.<br />

For a review, see Cork (2000) .<br />

K . <strong>Clinical</strong> Diagnosis <strong>of</strong> Liver Disease<br />

The index <strong>of</strong> suspicion <strong>of</strong> liver disease can be raised by the<br />

use <strong>of</strong> physical examination, plasma chemistry (enzymes,<br />

BA, TP, and PPE, galactose clearance test, and ultrasonography).<br />

However, to make a specific diagnosis, liver biopsy<br />

is the only method currently available (Lumeij, 1994a).<br />

VII . MUSCLE DISEASE<br />

Muscle enzyme pr<strong>of</strong>iles, half-lives <strong>of</strong> these enzymes in<br />

plasma, and plasma chemistry changes after experimentally<br />

induced muscle damage have been reported for racing<br />

pigeons (see Section VI.B). Enzyme pr<strong>of</strong>iles were<br />

studied for pectoral muscle, quadriceps muscle, and heart<br />

in pigeons and parrots ( Fig. 28-13 ). Creatine kinase (CK)<br />

was the most important enzyme in these three muscles,<br />

followed by LDH, AST, and ALT. Muscle damage was<br />

induced by injection <strong>of</strong> doxycycline in the pectoral muscle<br />

in pigeons ( Fig. 28-16 ). Creatine kinase activity in plasma<br />

was markedly elevated (about 20-fold) 16 h after injection.<br />

However, within 66h plasma activities <strong>of</strong> CK had returned<br />

to the maximum value <strong>of</strong> the reference range. LD activities<br />

were only slightly elevated (about tw<strong>of</strong>old) and only<br />

for about 40 h. AST activities showed a marked increase<br />

(about fourfold) for about 140 h, whereas ALT showed a<br />

marked increase (about fivefold) for about 214 h. Despite<br />

the fact that ALT activities in individual muscles are low,<br />

elevated plasma activities <strong>of</strong> this enzyme can be seen until<br />

9 days after muscle damage. Plasma CK activities, on the<br />

other hand, return to within the reference range within 3<br />

days after muscle damage, despite high tissue activities.<br />

LDH appeared to be a relatively poor indicator <strong>of</strong> muscle<br />

cell damage, despite relatively high activity <strong>of</strong> this enzyme<br />

in muscle ( Fig. 28-16 ). These findings can be explained by<br />

the differences in elimination half-lives <strong>of</strong> the respective<br />

enzymes (LDH 50 min, CK 3h, AST 7h, ALT 12 h; Tables<br />

28-1 and 28-2 ).<br />

Not all elevated concentrations <strong>of</strong> muscle enzymes in<br />

plasma are an indication for muscle disease. Extreme muscular<br />

activity in the period preceding blood sampling is an<br />

important cause <strong>of</strong> elevated enzyme activities in plasma. In<br />

dogs, plasma CK activities increase approximately tw<strong>of</strong>old<br />

with exercise ( Heffron et al ., 1976 ). Trained persons have<br />

plasma CK activities that are twice those <strong>of</strong> more sedentary<br />

people ( Okinaka et al ., 1964 ). In humans, elevated activities<br />

<strong>of</strong> plasma CK can persist for about 1 week after exercise<br />

( Newham et al ., 1983 ). Chronic elevated plasma CK<br />

activities have been reported in certain occupational workers<br />

as a result <strong>of</strong> local muscular strain ( Brewster and De Visser,<br />

1988 ; Hagberg et al ., 1982 ). In healthy turkeys, plasma CK<br />

activity is extremely sensitive to physical exercise and stress.<br />

With controlled conditions <strong>of</strong> minimal exercise, stress, and<br />

time <strong>of</strong> handling, however, iatrogenic elevations <strong>of</strong> plasma<br />

CK activities can be prevented ( Tripp and Schmitz, 1982 ).<br />

Limited handling <strong>of</strong> penned mallards resulted in mean SD<br />

serum CK activities <strong>of</strong> 1325 1212 IU/L, whereas capture<br />

<strong>of</strong> wild mallards in entanglement nets resulted in serum CK<br />

activities <strong>of</strong> 12035 8125 IU/L, compared to 225 52 IU/L<br />

in control animals with minimal handling (Dabbert and<br />

Powll, 1993). Elevated plasma CK activities can be expected<br />

in birds with large muscle mass after capture stress (e.g.,<br />

ostrich). Intramuscular injections in birds are a well-known

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