Haematology, blood chemistry and urine parameters of free-ranging plains viscachas (Lagostomus maximus) in Argentina determined by use of a portable blood analyser (i-STAT) and conventional laboratory methods.

Haematology, blood chemistry and urine values were determined for 44 adult free-ranging plains viscachas (Lagostomus maximus; Rodentia, Chinchillidae) in their pampas habitat in central Argentina. The study animals were captured in the wild and anaesthetized with a ketamine-xylazine combination for physical examination and sampling. Blood was obtained by venipuncture of the saphenous vein. Results for many of the blood parameters fall within the reference ranges for pet chinchillas. Differentiation of white blood cells revealed a predominantly neutrophil count for plains viscachas, while chinchillas have predominantly lymphocytes. Mean values for blood urea nitrogen, creatinine, aspartate aminotransferase and sodium were higher than the upper limit of the reference range for pet chinchillas. The results of seven analytes (haematocrit, haemoglobin, glucose, blood urea nitrogen, sodium, potassium, chloride) were compared by using both a portable blood analyser (i-STAT) in the field and conventional laboratory methods. In general, correlation and agreement between the two methods were low for most parameters.

Seasonal acclimatization in water flux rate, urine osmolality and kidney water channels in free-living degus: molecular mechanisms, physiological processes and ecological implications.

The environmental modification of an organism's physiology in the field is often hypothesized to be responsible for allowing an organism to adjust to changing biotic and abiotic environmental conditions through increases in biological performance. Here, we examine the phenotypic flexibility of water flux rate, urine osmolality and the expression of kidney aquaporins (AQP; or water channels) in free-ranging Octodon degus, a South American desert-dwelling rodent, through an integrative study at cellular, systemic and organismal levels. Water flux rates varied seasonally and were significantly lower in austral summer than in winter, while urine osmolality was higher in summer than during winter. The observed water influx rate during summer was 10.3+/-2.3 ml day(-1) and during winter was 40.4+/-9.1 ml day(-1). Mean urine osmolality was 3137+/-472 mosmol kg(-1) during summer and 1123+/-472 mosmol kg(-1) during winter. AQP-2 medullary immunolabeling was more abundant in the kidneys of degus captured during summer than those captured during winter. This immunoreactivity was higher in apical cell membranes of medullary collecting ducts of degus in summer. AQP-1 immunostaining did not differ between seasons. Consistently, AQP-2 protein levels were increased in medulla from the summer individuals, as judged by the size of the 29 kDa band in the immunoblot. Here, we reveal how the integration of flexible mechanisms acting at cellular, systemic and organismal levels allows a small desert-dwelling mammal to cope with seasonal water scarcity in its semi-arid habitat.

Osmoregulation and water balance in the springhare (Pedetes capensis).

Springhares are large rodents that live in arid and semi-arid regions of Africa. We deprived springhares of water for periods of up to 7 days to determine what physiological adaptations. If any, enable them to survive in and regions without drinking. During water deprivation, springhares lost up to 30% body weight and produced a mean maximum urine concentration of 2548 mosmol kg-1 with a maximum of 3076 mosmol kg-1 in an individual animal. Haematocrit and plasma sodium and potassium concentrations were well regulated throughout water deprivation at 47.5 +/- 3.8% and 132.6 +/- 7.4 mmol l-1 and 3.5 +/- 0.7 mmol l-1, respectively, while plasma osmolality increased slightly from 293 +/- 12.5 mosmol kg-1 to 324 +/- 7.3 mosmol kg-1. Springhares thus appeared to be good osmoregulators and were able to maintain plasma volume during 7 days of water deprivation. In addition to the production of a relatively concentrated urine, water loss was limited by the lowered solute load and faecal water loss achieved by a reduction in food consumption and by the production of very dry faeces. These abilities, together with a favourable burrow microclimate and nocturnal activity pattern, enable them to survive in arid regions.

Clinical pathology and sample collection in the laboratory rodent.

Common laboratory rodents have always been a favorite choice as a pet. Although diagnostic clinical pathology has not been viewed as practical for the rodent patient, current advances in technology make processing of small samples possible. Cultivation of the technical skills necessary for rodent sample collection has the potential to improve the standard of rodent veterinary care. This article provides an overview of rodent sample collection techniques, hematology, clinical biochemistry, serology, and clinical pathology of other tissues and fluids for laboratory rodents. General principles of clinical pathology can be applied across species. This article emphasizes the subtleties of the different rodent species which may impact diagnostic interpretation.

Identification of the source of reagent variability in the xanthydrol/urea method.

Contamination of food and food packaging material by rodent urine is evidence of insanitary conditions. Urea from rodent urine is used as a chemical indicator of contamination. The limit of detection of the xanthydrol/urea AOAC Method 959.14 by formation of dixanthylurea crystals is 4 micrograms urea isolated from urine on packaging material. Six different lots of xanthydrol from 5 different manufacturers were compared. Differences in urea detection sensitivity of the xanthydrol of up to 1000-fold were observed. Melting points showed further evidence of variability and impurities in xanthydrol lots. A liquid chromatographic method was developed to separate and identify the impurities. Confirmation of analytes was performed by gas chromatography/mass spectrometry.

Sexual pheromones in lipids and other fractions from urine of the male mole rat, Spalax ehrenbergi.

Spalax ehrenbergi mole rats are blind, solitary, territorial, aggressive, subterranean rodents with a yearly breeding season that peaks in December and January. We confirm here an earlier report that estrous females are attracted to substances present in the urine of homospecific as compared to heterospecific adult males. We have also found that nonestrous female mole rats show avoidance behavior to the same homospecific urine. Our objective was to ascertain the nature of the pheromone(s) and gain insight as to its possible role in reproductive isolation and speciation. An active principle, detected in either two- or three-choice behavior tests, was found to be extractable from urine by methylene chloride (CH2Cl2) and mainly found in the neutral lipid fraction. Total lipids were chromatographed by thin layer chromatography on silica gel G60 plates. Most of the activity was found in a zone bounded by Rfs 0.2 and 0.7. Cholesterol, other sterols, and ethyl esters of fatty acids chromatographed in this zone as determined by standards and staining. Ethyl esters of fatty acids were also detected in this fraction by GC/MS analysis. Although a large amount of activity was found in lipids, it only accounted for about 1% of that found in urine. Some activity may have been destroyed or lost during the extraction procedure and some may remain in a lipid insoluble form. Preliminary tests of lipid extracts of various portions of the male urogenital tract revealed pheromonal activity present, particularly in tissues associated with testes, epididymis, prostate, and bladder.

Urinary characteristics of the Cape porcupine Hystrix africaeaustralis: effects of photoperiod and temperature.

The Cape porcupine Hystrix africaeaustralis is a large (11-18 kg), nocturnal, burrowing and group-living rodent. It experiences a metabolic response to seasonal acclimatization and is a hind gut fermenter. Changes in the urinary electrolyte and free urinary catecholamine concentrations of Cape porcupines were related to combined changes of ambient temperature and photoperiod regime. Three groups, A) Ta = 25 degrees C, 12L:12D; B) Ta = 32 degrees C, 16L:8D; C) Ta = 10 degrees C, 8L:16D, were studied to assess the influence of seasonal acclimatization on urinary bicarbonate and catecholamine concentrations. Urine volume was significantly (p < 0.001) higher in group C than in the other two groups. In groups B and C urinary pH was above 7 and this was associated with high concentrations of HCO3-. The total amount of catecholamines was higher in groups B and C than in group A. It is apparent that seasonal acclimatization of the Cape porcupine is also reflected by these parameters.

A field lab method to determine urine concentration in small mammals.

1. The concentrations of 136 urine samples from four species of small mammals were compared using osmometry, refractometry and a colorimetric test for urea concentration. 2. To obtain a wide range of concentrations (430-3950 mOsm/kg), urine samples were collected under normal and dehydration conditions. 3. Regression analyses of paired values indicate that measurements of total solids concentration (refractometric method) permit evaluations of urine osmolality and estimations of the concentration of urea with a high degree of confidence.

Urine analysis of three rodent species with emphasis on calcium and magnesium bicarbonate.

The urine composition of three rodent species, mole rat Spalax ehrenbergi, the golden hamster Mesocricetus auratus and the white rat Rattus norvegicus was studied. These three species represent different degrees of fossoriality. The results show that the urine of the species that show a higher degree of fossoriality, the mole rat and the hamster, contain high values of calcium and magnesium bicarbonates when compared with the white rat. From these results it may be assumed that the mole rat as well as the hamster can use the kidney as a pathway for releasing bicarbonate and carbonate. This mechanism may reduce the CO2 concentration in their hypercapnic environment.

[Population ecology of leptospires. 1. An experience with evaluation of leptospira count in a carrier and the intensity of elimination in the urine]. / K populiatsionnoi ékologii leptospir. Soobshchenie 1. Opyt otsenki chislennosti leptospir v organizme nositelia i intensivnosti vyvedeniia s mochoi.

The number of L. hebdomadis and L. grippotyphosa in the body of tundra voles (Microtus oeconomicus) has been shown to be approximately 500-800 million; about 100 million of them are daily eliminated from the body of a vole with urine. About 70% of the total volume and separate portions of urine contain leptospires, a single portion of urine containing about 2 million microbial cells. These data have proved to be the same for both L. hebdomadis and L. grippotyphosa.

Low-temperature urine collection apparatus for laboratory rodents.

An apparatus for the collection of urine at -19 degrees C from unrestrained small laboratory animals was developed. The cooling unit accommodated five rodent metabolism cages for the collection of urine volumes up to 50 ml per collection period. The unit operated continuously for 5--6 weeks with no maintenance other than removal of the urine specimens, cleaning of the cages and collection dishes, and provision of feed and water.