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

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592<br />

Chapter | 18 Pituitary Function<br />

test and directly by measuring plasma VP during hypertonic<br />

saline infusion. Both procedures are described here<br />

in detail, as they have been developed for use in the dog<br />

(Biewenga et al. , 1987 ; Mulnix et al. , 1976 ). It should be<br />

noted that because <strong>of</strong> interference <strong>of</strong> plasma proteins, the<br />

radioimmunoassay for VP requires prior extraction <strong>of</strong> the<br />

peptide with ethanol and validation <strong>of</strong> the assay for the dog<br />

(Biewenga et al. , 1991 ; Hellebrekers et al. , 1987 ). Antisera<br />

against AVP may possess 100% cross-reactivity with AVT<br />

( Choy and Watkins, 1986 ; Hellebrekers et al. , 1987 ).<br />

1 . Modifi ed Water-Deprivation Test<br />

a . Indication<br />

Differentiation between neurogenic and nephrogenic diabetes<br />

insipidus, when the administration <strong>of</strong> DDAVP (Minirin)<br />

has not resolved the diagnosis.<br />

b . Procedure<br />

Following 12 h <strong>of</strong> fasting, water is withheld and plasma<br />

and urine are collected every hour or 2 h, depending on the<br />

severity <strong>of</strong> the polyuria. Osmolality is measured in both<br />

samples. At each collection the animal is weighed. When<br />

the weight loss approaches 5% <strong>of</strong> initial body weight, the<br />

test should be stopped.<br />

When, in the presence <strong>of</strong> an adequate osmotic stimulus<br />

(Posm 305 mOsm/kg), urine concentration is maximal<br />

(less than 5% increase in Uosm between consecutive collections),<br />

2IU <strong>of</strong> lysine vasopressin are administered subcutaneously.<br />

Uosm is measured again 1h later.<br />

c . Interpretation<br />

In both nephrogenic diabetes insipidus and neurogenic<br />

diabetes insipidus, Uosm will remain low during water<br />

deprivation. In neurogenic diabetes insipidus, Uosm will<br />

rise by 50% or more following the injection <strong>of</strong> vasopressin,<br />

whereas in nephrogenic diabetes insipidus, there will<br />

be little or no rise in Uosm.<br />

However, as mentioned earlier, in some cases the outcome<br />

may not be conclusive and erroneous results may<br />

also occur.<br />

2 . VP Measurements during Hypertonic Saline Infusion<br />

a . Indications<br />

Differential diagnosis <strong>of</strong> polyuric conditions and suspicion<br />

<strong>of</strong> inappropriate VP secretion.<br />

b . Procedure<br />

The euhydrated animal is infused for 2 h via the jugular<br />

vein with 20% NaCl solution at a rate <strong>of</strong> 0.03 ml/kg body<br />

weight per minute. Samples for plasma VP and Posm<br />

are obtained at 20-minute intervals. Especially in the<br />

severely polyuric animal, there is a risk <strong>of</strong> inducing critical<br />

hypertonicity. In these cases the samples collected at 0, 40,<br />

and 80 min should be checked for Posm immediately.<br />

c . Interpretation<br />

The slope <strong>of</strong> the regression line for Posm and plasma VP<br />

concentration is used as a measure <strong>of</strong> the sensitivity <strong>of</strong> the<br />

osmoregulatory system. In the nomogram developed by<br />

Biewenga et al. , (1987), the 90% range for sensitivity was<br />

0.24 to 2.47 (pg/ml)/(mOsm/kg). The 90% range for the<br />

threshold <strong>of</strong> the system was 276 to 309 mOsm/kg. After<br />

hypophysectomy in the dog, there is no VP response to<br />

hypertonic saline infusion ( Meij et al. , 1997c ).<br />

However, as mentioned earlier, the occurrence <strong>of</strong> spontaneous<br />

VP pulses makes it difficult to differentiate these<br />

from VP pulses (to the magnitude <strong>of</strong> “ erratic bursts ”) during<br />

hypertonic saline infusion ( van Vonderen et al. , 2004b ).<br />

REFERENCES<br />

Agre , P. , King , L. S. , Yasui , M. , Guggino , W. B. , Ottersen , O. P. ,<br />

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channels—from atomic structure to clinical medicine. J. Physiol. 542 ,<br />

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Alam , S. M. , Ain , R. , Konno , T. , Ho-Chen , J. K. , and Soares , M. J.<br />

( 2006 ): The rat prolactin gene family locus: species-specific gene<br />

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Alexander , S. L. , Roud , H. K. , and Irvine , C. H. ( 1997 ). Effect <strong>of</strong><br />

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Amann , J. F. , Smith , R. M. , Ganjam , V. K. , Paull , W. K. , McClure , R. C. ,<br />

Green , E. M. , and Garner , H. E. ( 1987 ). Distribution and implications

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