Records |
Author |
Heistermann, M.; Palme, R.; Ganswindt, A. |
Title |
Comparison of different enzyme-immunoassays for assessment of adrenocortical activity in primates based on fecal analysis |
Type |
Journal Article |
Year |
2006 |
Publication |
American journal of primatology |
Abbreviated Journal |
Am. J. Primatol. |
Volume |
68 |
Issue |
3 |
Pages |
257-273 |
Keywords |
11-Hydroxycorticosteroids/*analysis; Adrenocorticotropic Hormone/pharmacology; Anesthesia; Animals; Corticosterone/analysis; Feces/*chemistry; Glucocorticoids/*analysis; Haplorhini/*metabolism; Hydrocortisone/analysis; Hypothalamo-Hypophyseal System/drug effects/physiology; Immunoenzyme Techniques/*methods; Pituitary-Adrenal System/drug effects/physiology; Species Specificity |
Abstract |
Most studies published to date that used fecal glucocorticoid measurements to assess adrenocortical activity in primate (and many nonprimate) species applied a specific cortisol or corticosterone assay. However, since these native glucocorticoids are virtually absent in the feces of most vertebrates, including primates, the validity of this approach has recently been questioned. Therefore, the overall aim of the present study was to assess the validity of four enzyme-immunoassays (EIAs) using antibodies raised against cortisol, corticosterone, and reduced cortisol metabolites (two group-specific antibodies) for assessing adrenocortical activity using fecal glucocorticoid metabolite (GCM) measurements in selected primate species (marmoset, long-tailed macaque, Barbary macaque, chimpanzee, and gorilla). Using physiological stimulation of the hypothalamo-pituitary-adrenocortical (HPA) axis by administering exogenous ACTH or anesthesia, we demonstrated that at least two assays detected the predicted increase in fecal GCM levels in response to treatment in each species. However, the magnitude of response varied between assays and species, and no one assay was applicable to all species. While the corticosterone assay generally was of only limited suitability for assessing glucocorticoid output, the specific cortisol assay was valuable for those species that (according to high-performance liquid chromatography (HPLC) analysis data) excreted clearly detectable amounts of authentic cortisol into the feces. In contrast, in species in which cortisol was virtually absent in the feces, group-specific assays provided a much stronger signal, and these assays also performed well in the other primate species tested (except the marmoset). Collectively, the data suggest that the reliability of a given fecal glucocorticoid assay in reflecting activity of the HPA axis in primates clearly depends on the species in question. Although to date there is no single assay system that can be used successfully across species, our data suggest that group-specific assays have a high potential for cross-species application. Nevertheless, regardless of which GC antibody is chosen, our study clearly reinforces the necessity of appropriately validating the respective assay system before it is used. |
Address |
Department of Reproductive Biology, German Primate Center, Gottingen, Germany. mheiste@gwdg.de |
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English |
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0275-2565 |
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PMID:16477600 |
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no |
Call Number |
Equine Behaviour @ team @ |
Serial |
4078 |
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Author |
Polley, L. |
Title |
Strongylid parasites of horses: experimental ecology of the free-living stages on the Canadian prairie |
Type |
Journal Article |
Year |
1986 |
Publication |
American Journal of Veterinary Research |
Abbreviated Journal |
Am J Vet Res |
Volume |
47 |
Issue |
8 |
Pages |
1686-1693 |
Keywords |
Animals; Canada; Ecology; Feces; Female; Horse Diseases/*epidemiology/parasitology; Horses; Larva; Ovum/cytology; Seasons; Strongyloides/isolation & purification; Strongyloidiasis/epidemiology/*veterinary |
Abstract |
Each month for a 1-year period (October through September), equine fecal masses containing eggs of strongylid nematodes were placed outdoors on small grass plots in Saskatchewan, Canada. Thereafter, feces and grass from the plots were sampled after intervals of 1 week or longer, and the strongylid eggs and larvae recovered were counted. These observations were made over a 2-year period. Development of eggs to infective larvae occurred in all experiments, except those established in October, December, and January. Infective larvae from experiments set up in April through September survived that winter. During the summer, there was a gradual build up of infective larvae in the fecal masses, which reached a peak in August and September and then decreased into the winter. These results are discussed in the context of the control of strongylid parasites of horses on the Canadian prairie and in other areas of the world with a similar climate and similar horse management practices. |
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English |
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ISSN |
0002-9645 |
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Notes |
PMID:3752676 |
Approved |
no |
Call Number |
Equine Behaviour @ team @ |
Serial |
2682 |
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Author |
Manning, G.S.; Ratanarat, C. |
Title |
Fasciolopsis buski (Lankester, 1857) in Thailand |
Type |
Journal Article |
Year |
1970 |
Publication |
The American Journal of Tropical Medicine and Hygiene |
Abbreviated Journal |
Am J Trop Med Hyg |
Volume |
19 |
Issue |
4 |
Pages |
613-619 |
Keywords |
Adolescent; Adult; Aged; Animals; Buffaloes; Cattle; Child; Child, Preschool; *Disease Reservoirs; Dogs; Ecology; *Fasciolidae; Feces; Female; Health Surveys; Horses; Humans; Infant; Infant, Newborn; Male; Middle Aged; *Plants, Edible; Sex Factors; *Snails; Swine; Thailand; Trematode Infections/*epidemiology |
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ISSN |
0002-9637 |
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Notes |
PMID:5425498 |
Approved |
no |
Call Number |
Equine Behaviour @ team @ |
Serial |
2734 |
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Author |
Carlsson, H.-E.; Lyberg, K.; Royo, F.; Hau, J. |
Title |
Quantification of stress sensitive markers in single fecal samples do not accurately predict excretion of these in the pig |
Type |
Journal Article |
Year |
2007 |
Publication |
Research in Veterinary Science |
Abbreviated Journal |
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Volume |
82 |
Issue |
3 |
Pages |
423-428 |
Keywords |
Cortisol; Immunoglobulin A; Stress; Pigs; Feces; Animal welfare |
Abstract |
All feces produced during 24 h were collected from five pigs and cortisol and immunoreactive cortisol metabolites (CICM), and IgA were quantified. Within pigs, the concentrations of CICM and IgA varied extensively between random samples obtained from a single fecal dropping, and deviated in most cases significantly from the true concentration measured in total fecal output (CV 6.7–130%). The CICM and IgA contents varied considerably (CV 8.1–114%) within and between individual fecal droppings from the same pig compared to the total fecal excretion. In conclusion, single random samples could not be used to reliably quantify the total fecal concentration or excretion of CICM or IgA in pigs. Analyses of all feces collected during shorter periods than 24 h did not provide an accurate estimate of the daily excretion of CICM. Thus, the concentration of stress sensitive molecules in random single fecal samples as an indicator of animal welfare should be interpreted with prudence. |
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ISSN |
0034-5288 |
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no |
Call Number |
Equine Behaviour @ team @ |
Serial |
5853 |
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Author |
Vetvik, H.; Grewal, H.M.S.; Haugen, I.L.; Åhrén, C.; Haneberg, B. |
Title |
Mucosal antibodies can be measured in air-dried samples of saliva and feces |
Type |
Journal Article |
Year |
1998 |
Publication |
Journal of Immunological Methods |
Abbreviated Journal |
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Volume |
215 |
Issue |
1–2 |
Pages |
163-172 |
Keywords |
Saliva; Feces; IgA; IgG; Air-drying |
Abstract |
IgA antibodies reflecting airways or intestinal mucosal immune responses can be found in saliva and feces, respectively, and IgG antibodies reflecting serum antibodies can be found in saliva. In this study, antibodies were detected in samples of saliva and feces which had been air-dried at room temperature (+20°C) or +37°C, and stored at these temperatures for up to 6 months. In saliva the antibody levels increased, while the antibodies in feces decreased upon storage. The individual IgA antibody concentrations which were adjusted by using the ratios of specific IgA/total IgA were relatively stable in both saliva and feces, and correlated with corresponding antibody levels in samples which had been stored at -20°C. The results indicate that air-dried saliva and feces can be used for semiquantitative measurements of mucosal antibodies, even after prolonged storage at high temperatures and lack of refrigeration. |
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Edition |
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ISSN |
0022-1759 |
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no |
Call Number |
Equine Behaviour @ team @ |
Serial |
5996 |
Permanent link to this record |