A new experimental mouse model of water intoxication with sustained increased intracranial pressure and mild hyponatremia without side effects of antidiuretics

• Published in: Experimental Animals Vol. 69; no. 1; pp. 92 - 103
• Main Authors: Bordoni, Luca, Jiménez, Eugenio Gutiérrez, Nielsen, Søren, Østergaard, Leif, Frische, Sebastian
• Format: Journal Article
• Language: English
• Published: Japan Japanese Association for Laboratory Animal Science 01.01.2020; Japan Science and Technology Agency
• Subjects: Acetic acid; Animals; Antidiuretic Agents - administration & dosage; Antidiuretics; Blood pressure; Body weight; Brain stem; Deamino Arginine Vasopressin - administration & dosage; Desmopressin; Disease Models, Animal; Diuresis; Extreme values; Hyponatremia; Hyponatremia - chemically induced; Hyponatremia - physiopathology; Injection; Injections, Intraperitoneal; Intoxication; Intracranial Hypertension - chemically induced; Intracranial Hypertension - physiopathology; Intracranial Pressure; Male; Mice; Mice, Inbred C57BL; mouse model; Original; Potassium chloride; Side effects; Sodium bicarbonate; Sodium chloride; Urine; water intoxication; Water Intoxication - physiopathology; intracranial pressure; mouse model; water intoxication; hyponatremia; desmopressin
• ISSN: 1341-1357; 1881-7122
• DOI: 10.1538/expanim.19-0040

The most used experimental mouse model of hyponatremia and elevated intracranial pressure (ICP) is intraperitoneal injection of water in combination with antidiuretics. This model of water intoxication (WI) results in extreme pathological changes and death within 1 h. To improve preclinical studies of the pathophysiology of elevated ICP, we characterized diuresis, cardiovascular parameters, blood ionogram and effects of antidiuretics in this model. We subsequently developed a new mouse model with mild hyponatremia and sustained increased ICP. To investigate the classical protocol (severe WI), C57BL/6mice were anesthetized and received an intraperitoneal injection of 20% body weight of MilliQ water with or without 0.4 µg·kg−1 desmopressin acetate (dDAVP). Corresponding Sham groups were also studied. In the new WI protocol (mild WI), 10% body weight of a solution containing 6.5 mM NaHCO3, 1.125 mM KCl and 29.75 mM NaCl was intraperitoneally injected. By severe WI, ICP and mean arterial pressure increased until brain stem herniation occurred (23 ± 3 min after injection). The cardiovascular effects were accelerated by dDAVP. Severe WI induced a halt to urine production irrespective of the use of dDAVP. Following the new mild WI protocol, ICP also increased but was sustained at a pathologically high level without inducing herniation. Mean arterial pressure and urine production were not affected during mild WI. In conclusion, the new mild WI protocol is a superior experimental model to study the pathophysiological effects of elevated ICP induced by water intoxication.