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Author Goldman, Alvin I.
Title A Causal Theory of Knowing Type Journal Article
Year 1967 Publication (down) The Journal of Philosophy Abbreviated Journal
Volume 64 Issue 12 Pages 357-372
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Notes Approved no
Call Number Equine Behaviour @ team @ Serial 4194
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Author Crosby, M.B.; Svenson, J.L.; Zhang, J.; Nicol, C.J.; Gonzalez, F.J.; Gilkeson, G.S.
Title Peroxisome proliferation-activated receptor (PPAR)gamma is not necessary for synthetic PPARgamma agonist inhibition of inducible nitric-oxide synthase and nitric oxide Type Journal Article
Year 2005 Publication (down) The Journal of pharmacology and experimental therapeutics Abbreviated Journal J Pharmacol Exp Ther
Volume 312 Issue 1 Pages 69-76
Keywords Animals; Cell Line; Gene Expression/drug effects; Macrophages/drug effects/metabolism; Mice; Mice, Inbred C57BL; Nitric Oxide/*metabolism; Nitric Oxide Synthase/*metabolism; Nitric Oxide Synthase Type II; PPAR delta/metabolism; PPAR gamma/*agonists/deficiency; Thiazolidinediones/pharmacology
Abstract Peroxisome proliferation-activated receptor (PPAR)gamma agonists inhibit inducible nitric-oxide synthase (iNOS), tumor necrosis factor-alpha, and interleukin-6. Because of these effects, synthetic PPARgamma agonists, including thiazolidinediones, are being studied for their impact on inflammatory disease. The anti-inflammatory concentrations of synthetic PPARgamma agonists range from 10 to 50 microM, whereas their binding affinity for PPARgamma is in the nanomolar range. The specificity of synthetic PPARgamma agonists for PPARgamma at the concentrations necessary for anti-inflammatory effects is thus in question. We report that PPARgamma is not necessary for the inhibition of iNOS by synthetic PPARgamma agonists. RAW 264.7 macrophages possess little PPARgamma, yet lipopolysaccharide (LPS)/interferon (IFN)gamma-induced iNOS was inhibited by synthetic PPARgamma agonists at 20 microM. Endogenous PPARgamma was inhibited by the transfection of a dominant-negative PPARgamma construct into murine mesangial cells. In the transfected cells, synthetic PPARgamma agonists inhibited iNOS production at 10 microM, similar to nontransfected cells. Using cells from PPARgamma Cre/lox conditional knockout mice, baseline and LPS/IFNgamma-induced nitric oxide levels were higher in macrophages lacking PPARgamma versus controls. However, synthetic PPARgamma agonists inhibited iNOS at 10 microM in the PPARgamma-deficient cells, similar to macrophages from wild-type mice. These results indicate that PPARgamma is not necessary for inhibition of iNOS expression by synthetic PPARgamma agonists at concentrations over 10 microM. Intrinsic PPARgamma function, in the absence of synthetic agonists, however, may play a role in inflammatory modulation.
Address Department of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA
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ISSN 0022-3565 ISBN Medium
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Notes PMID:15356214 Approved no
Call Number refbase @ user @ Serial 73
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Author Wilhelm, W.E.; Anderson, J.H.
Title Vahlkampfia lobospinosa (Craig. 1912) Craig. 1913: rediscovery of a coprozoic ameba Type Journal Article
Year 1971 Publication (down) The Journal of Parasitology Abbreviated Journal J Parasitol
Volume 57 Issue 6 Pages 1378-1379
Keywords Animals; Cattle; Ecology; Feces/microbiology; Horse Diseases/epidemiology; Horses; Protozoan Infections/epidemiology; *Protozoan Infections, Animal; Sarcodina/*classification/growth & development; Swine; Swine Diseases/epidemiology; Tennessee
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ISSN 0022-3395 ISBN Medium
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Notes PMID:5157177 Approved no
Call Number Equine Behaviour @ team @ Serial 2724
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Author Walker, M.L.; Becklund, W.W.
Title Occurrence of a cattle eyeworm, Thelazia gulosa (Nematoda: Thelaziidae), in an imported giraffe in California and T. lacrymalis in a native horse in Maryland Type Journal Article
Year 1971 Publication (down) The Journal of Parasitology Abbreviated Journal J Parasitol
Volume 57 Issue 6 Pages 1362-1363
Keywords Animals; *Animals, Zoo; Artiodactyla; California; Ecology; Eye Diseases/epidemiology/*veterinary; Female; Horse Diseases/*epidemiology; Horses; Male; Maryland; Nematode Infections/epidemiology/*veterinary; Spiruroidea/*classification
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ISSN 0022-3395 ISBN Medium
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Notes PMID:5157171 Approved no
Call Number Equine Behaviour @ team @ Serial 2725
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Author Malek, E.A.
Title The life cycle of Gastrodiscus aegyptiacus (Cobbold, 1876) Looss, 1896 (Trematoda: Paramphistomatidae: Gastrodiscinae) Type Journal Article
Year 1971 Publication (down) The Journal of Parasitology Abbreviated Journal J Parasitol
Volume 57 Issue 5 Pages 975-979
Keywords Animals; Bulinus; *Disease Vectors; Ecology; Feces; Female; Horse Diseases/*etiology; Horses; Metamorphosis, Biological; Ovum; Parasite Egg Count; Perissodactyla; Sudan; Trematoda/anatomy & histology/growth & development; Trematode Infections/etiology/*veterinary
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ISSN 0022-3395 ISBN Medium
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Notes PMID:5167379 Approved no
Call Number Equine Behaviour @ team @ Serial 2726
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Author Hoogstraal, H.; Mitchell, R.M.
Title Haemaphysalis (Alloceraea) aponommoides Warburton (Ixodoidea: Ixodidae), description of immature stages, hosts, distribution, and ecology in India, Nepal, Sikkim, and China Type Journal Article
Year 1971 Publication (down) The Journal of Parasitology Abbreviated Journal J Parasitol
Volume 57 Issue 3 Pages 635-645
Keywords Altitude; Animals; Artiodactyla; Birds; Buffaloes; Carnivora; Cattle; China; Deer; Dogs; Ecology; Female; Goats; Horses; Humans; India; Insectivora; Larva/anatomy & histology; Male; Mice; Nepal; Rats; Rodentia; Sciuridae; Seasons; Sheep; Tick Infestations/*epidemiology; Ticks/*anatomy & histology/growth & development
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ISSN 0022-3395 ISBN Medium
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Notes PMID:5090972 Approved no
Call Number Equine Behaviour @ team @ Serial 2730
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Author Hoogstraal, H.; Dhanda, V.; Bhat, H.R.
Title Haemaphysalis (Kaiseriana) davisi sp. n. (Ixodoidea: Ixodidae), a parasite of domestic and wild mammals in Northeastern India, Sikkim, and Burma Type Journal Article
Year 1970 Publication (down) The Journal of Parasitology Abbreviated Journal J Parasitol
Volume 56 Issue 3 Pages 588-595
Keywords Animals; Cattle; Cattle Diseases/etiology; Deer; Ecology; Goats; Horse Diseases/etiology; Horses; India; Mammals; Myanmar; Sheep; Sheep Diseases/etiology; Tick Infestations; Ticks/*classification/isolation & purification
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ISSN 0022-3395 ISBN Medium
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Notes PMID:4246255 Approved no
Call Number Equine Behaviour @ team @ Serial 2736
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Author Dierenfeld, E.S.
Title Vitamin E in exotics: effects, evaluation and ecology Type Journal Article
Year 1994 Publication (down) The Journal of Nutrition Abbreviated Journal J Nutr
Volume 124 Issue 12 Suppl Pages 2579s-2581s
Keywords Animal Feed/*analysis; Animals; Animals, Zoo/blood/*metabolism; Antelopes/blood/metabolism; Birds/blood/metabolism; Deer/blood/metabolism; Elephants/blood/metabolism; Equidae/blood/metabolism; Perissodactyla/blood/metabolism; Vitamin E/*administration & dosage/analysis/blood; Vitamin E Deficiency/pathology/physiopathology/veterinary
Abstract The pathophysiology and lesions associated with vitamin E deficiency are similar between domestic and exotic species, and circulating plasma concentrations are also similar between comparable groups. However, many ecological variables must be considered for the most relevant comparisons. Tissue values of vitamin E, apart from plasma, are unknown for most exotics. Dietary vitamin E requirements of exotic species and domestics appear to differ; based on natural foodstuff analyses and clinical observations, between 50 and 200 mg vitamin E/kg DM are necessary to prevent vitamin E deficiency, 5- to 10-fold higher than current livestock recommendations.
Address Department of Nutrition, Wildlife Health Center, Wildlife Conservation Society, Bronx, NY 10460
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ISSN 0022-3166 ISBN Medium
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Notes PMID:7996243 Approved no
Call Number Equine Behaviour @ team @ Serial 2661
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Author Tang, A.C.; Reeb, B.C.; Romeo, R.D.; McEwen, B.S.
Title Modification of Social Memory, Hypothalamic-Pituitary-Adrenal Axis, and Brain Asymmetry by Neonatal Novelty Exposure Type Journal Article
Year 2003 Publication (down) The Journal of Neuroscience Abbreviated Journal
Volume 23 Issue 23 Pages 8254-8260
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Abstract Although corticosterone (a stress hormone) is known to influence social behavior and memory processes, little has been explored concerning its modulatory role in social recognition. In rats, social recognition memory for conspecifics typically lasts <2 hr when evaluated using a habituation paradigm. Using neonatal novelty exposure, a brief and transient early life stimulation method known to produce long-lasting changes in the hypothalamic-pituitary-adrenal axis, we found that social recognition memory was prolonged to at least 24 hr during adulthood. This prolonged social memory was paralleled by a reduction in the basal blood concentration of corticosterone. The same neonatal stimulation also resulted in a functional asymmetry expressed as a greater right-turn preference in a novel environment. Rats that preferred to turn right showed better social recognition memory. These inter-related changes in basal blood corticosterone concentration, turning asymmetry, and social recognition memory suggest that stress hormones and brain asymmetry are likely candidates for modulating social memory. Furthermore, given that neonatal stimulation has been shown to improve learning and memory performance primarily under aversive learning situations, the neonatal novelty exposure-induced enhancement in social recognition broadens the impact of early life stimulation to include the social domain.
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Call Number Equine Behaviour @ team @ Serial 5754
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Author Hieshima, K.; Kawasaki, Y.; Hanamoto, H.; Nakayama, T.; Nagakubo, D.; Kanamaru, A.; Yoshie, O.
Title CC Chemokine Ligands 25 and 28 Play Essential Roles in Intestinal Extravasation of IgA Antibody-Secreting Cells Type Journal Article
Year 2004 Publication (down) The Journal of Immunology Abbreviated Journal
Volume 173 Issue 6 Pages 3668-3675
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Abstract CCL25 (also known as thymus-expressed chemokine) and CCL28 (also known as mucosae-associated epithelial chemokine) play important roles in mucosal immunity by recruiting IgA Ab-secreting cells (ASCs) into mucosal lamina propria. However, their exact roles in vivo still remain to be defined. In this study, we first demonstrated in mice that IgA ASCs in small intestine expressed CCR9, CCR10, and CXCR4 on the cell surface and migrated to their respective ligands CCL25, CCL28, and CXCL12 (also known as stromal cell-derived factor 1), whereas IgA ASCs in colon mainly expressed CCR10 and CXCR4 and migrated to CCL28 and CXCL12. Reciprocally, the epithelial cells of small intestine were immunologically positive for CCL25 and CCL28, whereas those of colon were positive for CCL28 and CXCL12. Furthermore, the venular endothelial cells in small intestine were positive for CCL25 and CCL28, whereas those in colon were positive for CCL28, suggesting their direct roles in extravasation of IgA ASCs. Consistently, in mice orally immunized with cholera toxin (CT), anti-CCL25 suppressed homing of CT-specific IgA ASCs into small intestine, whereas anti-CCL28 suppressed homing of CT-specific IgA ASCs into both small intestine and colon. Reciprocally, CT-specific ASCs and IgA titers in the blood were increased in mice treated with anti-CCL25 or anti-CCL28. Anti-CXCL12 had no such effects. Finally, both CCL25 and CCL28 were capable of enhancing α4 integrin-dependent adhesion of IgA ASCs to mucosal addressin cell adhesion molecule-1 and VCAM-1. Collectively, CCL25 and CCL28 play essential roles in intestinal homing of IgA ASCs primarily by mediating their extravasation into intestinal lamina propria.
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Notes 10.4049/jimmunol.173.6.3668 Approved no
Call Number Equine Behaviour @ team @ Serial 6011
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