EFFECTS OF SEX, ENVIRONMENT, AND CONDITION ON THE MUSKING BEHAVIOR OF SYMPATRIC GARTERSNAKES (THAMNOPHIS SPP.)

Despite an abundance of studies documenting antipredator and defensive behaviors of gartersnakes (genus Thamnophis), few have quantitatively examined musking, a widely utilized antipredator tactic. In this study we quantify musking behaviors in the Terrestrial Gartersnake (Thamnophis elegans) and the Plains Gartersnake (T. radix) when hand-captured at four sites in and near Denver, Colorado, USA. Overall, Plains Gartersnakes musked significantly more often than Terrestrial Gartersnakes. Female Terrestrial Gartersnakes musked more frequently than males, a pattern not evident in the Plains Gartersnake. Additionally, we observed a positive correlation in body condition and musking propensity in Terrestrial Gartersnakes, suggesting resource-dependent behavior in this species. Musking behavior was consistent across variations in predation pressure, environmental conditions, and snake body size, all factors shown to influence other gartersnake defensive behaviors. These results corroborate other research which demonstrates that snake antipredator behaviors are determined by complex interactions of abiotic and biotic factors

Glomerular sieving of anionic and neutral bovine albumins in proteinuric rats

Glomerular sieving of anionic and neutral bovine albumins in proteinuric rats. To characterize the defect in glomerular permeability leading to albuminuria in rats made nephrotic acutely by infusion of hexadimethrine (HDM) or chronically by administration of Adriamycin® (doxorubicin) (Adria), we developed and validated a tissue accumulation method for simultaneous determination of the glomerular sieving coefficients (GSC) of anionic 131I-labeled bovine albumin (BSA-pI 4.9) and 125I-labeled charge-modified neutral BSA (nBSA-pI 7.5 to 8.0). Total filtered marker was calculated by adding marker excreted in the urine to that filtered but reabsorbed by the tubules. The latter was determined by subtracting interstitial marker present in the left kidney, rendered non-filtering by ureteral ligation during mannitol diuresis, from the total marker accumulating within the right, filtering kidney. Experiments showed that markers circulated and were excreted intact and were neither degraded nor deiodinated during the period of the clearance studies.In control animals the GSC of nBSA (0.026 ± 0.004) greatly exceeded that of BSA (0.0006 ± 0.0002), demonstrating the normal charge dependence of permeability. Both proteinuric groups had marked increases in the GSC of BSA (HDM: 0.021 ± 0.005; Adria: 0.025 ± 0.004), which correlated with appearance of rat albumin in their urine. HDM rats also had a twofold increase in the GSC of nBSA (0.049 ± 0.005), indicating alteration of the size dependence of permeability. The absolute increase of GSC of BSA and nBSA was similar, suggesting that albuminuria resulted from appearance of new “pores” in the glomerular filter that were not charge selective for proteins of the size of albumin. Thus, infusion of HDM, which binds to and neutralizes GBM anions, appears to produce albuminuria by inducing a structural change in the glomerular filter. Conversely, Adria rats had no significant increase in the GSC of nBSA (0.031 ± 0.005), indicating no significant change in the size dependence of permeability for proteins of the size of albumin. In these animals, the GSC of the anionic BSA approached that of the neutral nBSA, indicating that Adriamycin induces albuminuria by markedly reducing the normal charge dependence of permeability

Experimental glomerulonephritis induced by hydrocarbon exposure: A systematic review

BACKGROUND: Much epidemiological evidence suggests that hydrocarbon exposure may induce glomerulonephritis and worsen its course in many patients. The mechanisms are unknown, however, no specific microscopic pattern has been identified, and it has also been argued that hydrocarbon exposure causes tubular damage mainly. Studying experimental animals may best answer these questions, and as no systematic review of glomerulonephritis produced experimentally by hydrocarbon exposure has been performed previously, I found it relevant to search for and analyse such studies. METHODS: Animal experiments having mimicked human glomerulonephritis by hydrocarbon exposure were sought on Medline and Toxnet RESULTS: Twenty-six experiments using thirteen different hydrocarbons were identified. Several human subtypes were observed including IgA nephritis, mesangial, proliferative and extracapillary glomerulonephritis, focal and focal-segmental sclerosis, minimal change nephropathy, anti-GBM and anti-TBM nephritis, and glomerulonephritis associated with peiarteritis nodosa. Glomerular proteinuria was seen in 10/12 experiments that included urine analyses, and renal failure in 5/8 experiments that included measurements of glomerular function. All experiments resulted in various degrees of tubular damage as well. In most studies, where the animals were examined at different times during or after the exposure, the renal microscopic and functional changes were seen immediately, whereas deposits of complement and immunoglobulins appeared late in the course, if at all. CONCLUSION: These experiments are in accord with epidemiological evidence that hydrocarbon exposure may cause glomerulonephritis and worsen renal function. Probable mechanisms include an induction of autologous antibodies and a disturbance of normal immunological functions. Also, tubular damage may increase postglomerular resistance, resulting in a glomerular deposition of macromolecules. In most models a causal role of glomerular immune complex formation was unlikely, but may rather have been a secondary phenomenon. As most glomerulonephritis subgroups were seen and as some of the hydrocarbons produced more than one subgroup, the microscopic findings in a patient cannot be used as a clue to the causation of his disease. By the same reason, the lack of a specific histological pattern in patients with glomerulonephritis assumed to have been caused by hydrocarbon exposure is not contradictive

A monoclonal antibody against GBM heparan sulfate induces an acute selective proteinuria in rats

A monoclonal antibody against GBM heparan sulfate induces an acute selective proteinuria in rats. After immunization of mice with partially-purified heparan sulfate proteoglycan (HSPG) isolated from rat glomeruli, a monoclonal antibody (mAb JM-403) was obtained, which was directed against heparan sulfate (HS), the glycosaminoglycan side chain of HSPG. In ELISA it reacted with isolated human glomerular basement membrane (GBM) HSPG, HS and hyaluronic acid, but not with the core protein of human GBM HSPG, and not with chondroitin sulfate A and C, dermatan sulfate, keratan sulfate and heparin. Furthermore, it did not bind to laminin, collagen type IV or fibronectin. Specificity of JM-403 for HS was also suggested by results of inhibition studies, which found that intact HSPG and HS, but not the core protein, inhibited the binding of JM-403 to HS. In indirect immunofluorescence on cryostat sections of rat kidney, a fine granular to linear staining of the GBM was observed, along with a variable staining of the other renal basement membranes. Pretreatment of the sections with heparitinase completely prevented the binding of mAb JM-403, whereas pretreatment with chondroitinase ABC or hyaluronidase had no effect. The precise binding site of mAb JM-403 was investigated by indirect immunoelec-tron microscopy. It revealed a diffuse staining of the whole width of the GBM. One hour after intravenous injection of JM-403 into rats, the mAb was detected along the glomerular capillary wall in a fine granular pattern, which shifted towards a more mesangial localization after 24 hours. No binding was observed anymore by day 15. Intravenous injection induced a dose-dependent, transient and selective proteinuria that was maximal immediately after the injection. Administration of 2 mg of JM-403 increased the urinary albumin excretion within the first 24 hours after injection from (mean ± SD) 177 ± 19 to 20,755 ± 10,310 µg/24 hr (P < 0.01); the urinary IgG excretion increased from 5.8 ± 2.9 to 236.1 ± 132.2 µg/24 hr (P < 0.03); the selectivity index (clearance IgG/clearance albumin) decreased from 0.33 ± 0.12 to 0.12 ± 0.05 (P < 0.004)

Evaluation of high-resolution satellite precipitation products with ground-based measurements over Europe

Determining water quantity of precipitation, spatially and temporally is fundamental for weather forecasting, applications in hydrology and meteorology, climate science and for agriculture and industry. Only satellite measurements from space are able to perform large-scale measurements covering both, ocean and land. In order to prove the reliability of the satellite data for application, but also to develop and improve the satellite retrievals of precipitation data, the satellite products need to be evaluated with reliable ground-based measurements. The high-resolution satellite data that this study is based on, was provided at a global scale by the satellite network Global Precipitation Measurement (GPM) that builds an international constellation of research and operational satellites. Previous evaluation of GPM dataset have shown error characteristics, related to topography, climate and latitude, that are potentially linking back to the sensor input, such as the calibrated passive microwave estimates (PMW), being a fundamental source for the final product. Evaluating the PMW estimates over a large region can improve the understanding of the error sources in the combined final GPM product. This study evaluated the calibrated PMW estimates (the primary foundation of the GPM IMERG final product) over Europe for the period from March 2014 to the end of December 2019 by using the blended gauge data from, provided by European Climate Assessment and Dataset (ECA&D), as reference. The data was evaluated seasonally, conducting different error indices to compare the satellite product with the gauge data and linking it to topography, climate and latitude. The results showed clear relationships between PMW data accuracy with elevation and climate zones in Europe, that can be linked to difficulties for PMW sensors to measure e.g. frozen precipitation, observe from a cold background, or when convection occurs in warmer climates. Also, for the relation to latitude, a worse performance with latitude was found, however only in winter, when frozen precipitation is likely at higher latitudes. Correcting those input sources, based on accuracy assessments, such as it was assessed by this study, can be meaningful for further improving GPM product