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Author Jordan, J.
Title [Modern views on the structure and function of the vomeronasal (Jacobson's) organ in mammals] Type Journal Article
Year 1970 Publication (up) Otolaryngologia Polska. The Polish Otolaryngology Abbreviated Journal Otolaryngol Pol
Volume 24 Issue 4 Pages 457-462
Keywords Animals; Cats; Dogs; Guinea Pigs; Horses; Humans; Mice; Nasal Septum/anatomy & histology/blood supply/cytology/innervation/physiology; Nose/*anatomy & histology/blood supply/innervation/*physiology; Rabbits; Rats; Sheep; Smell
Abstract
Address
Corporate Author Thesis
Publisher Place of Publication Editor
Language Polish Summary Language Original Title Obecne poglady na budowe i czynnosc narzadu lemieszowo-nosowego (Jacobsona) u ssakow
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0030-6657 ISBN Medium
Area Expedition Conference
Notes PMID:4918960 Approved no
Call Number Equine Behaviour @ team @ Serial 4315
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Author Miller, G.
Title Animal behavior. Signs of empathy seen in mice Type Journal Article
Year 2006 Publication (up) Science (New York, N.Y.) Abbreviated Journal Science
Volume 312 Issue 5782 Pages 1860-1861
Keywords Altruism; Animals; Behavior, Animal; *Empathy; Formaldehyde/administration & dosage; Mice/*psychology; Motivation; Pain/*psychology; *Social Behavior
Abstract
Address
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 1095-9203 ISBN Medium
Area Expedition Conference
Notes PMID:16809499 Approved no
Call Number refbase @ user @ Serial 461
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Author Scherer, W.F.; Dickerman, R.W.
Title Ecologic studies of Venezuelan encephalitis virus in southeastern Mexico. 8. Correlations and conclusions Type Journal Article
Year 1972 Publication (up) The American Journal of Tropical Medicine and Hygiene Abbreviated Journal Am J Trop Med Hyg
Volume 21 Issue 2 Pages 86-89
Keywords Animals; Birds; Cattle; Chiroptera; Cricetinae; Culex; Culicidae; *Disease Reservoirs; Ecology; Encephalitis Virus, Venezuelan Equine/immunology; Encephalitis Viruses/*isolation & purification; Encephalomyelitis, Equine/epidemiology/*etiology; Horses; Humans; *Insect Vectors; Mammals; Mexico; Mice; Opossums; Rats; Swine
Abstract
Address
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0002-9637 ISBN Medium
Area Expedition Conference
Notes PMID:4399844 Approved no
Call Number Equine Behaviour @ team @ Serial 2721
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Author Houpt, K.A.
Title Animal behavior as a subject for veterinary students Type Journal Article
Year 1976 Publication (up) The Cornell veterinarian Abbreviated Journal Cornell Vet
Volume 66 Issue 1 Pages 73-81
Keywords Aggression; Animals; *Behavior, Animal; Cats; Chickens; Dogs; Education, Veterinary; Goats; Horses; Humans; Maternal Behavior; Mice; New York; Sexual Behavior, Animal; Sheep; Sleep; Social Behavior; Social Dominance; Swine
Abstract Knowledge of animal behavior is an important asset for the veterinarian; therefore a course in veterinary animal behavior is offered at the New York State College of Veterinary Medicine as an elective. The course emphasizes the behavior of those species of most interest to the practicing veterinarian: cats, dogs, horses, cows, pigs and sheep. Dominance heirarchies, animal communication, aggressive behavior, sexual behavior and maternal behavior are discussed. Play, learning, diurnal cycles of activity and sleep, and controls of ingestive behavior are also considered. Exotic and zoo animal behaviors are also presented by experts in these fields. The critical periods of canine development are related to the optimum management of puppies. The behavior of feral dogs and horses is described. The role of the veterinarian in preventing cruelty to animals and recognition of pain in animals is emphasized. Whenever possible behavior is observed in the laboratory or on film.
Address
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0010-8901 ISBN Medium
Area Expedition Conference
Notes PMID:767053 Approved no
Call Number refbase @ user @ Serial 61
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Author Gavrilova, O.; Haluzik, M.; Matsusue, K.; Cutson, J.J.; Johnson, L.; Dietz, K.R.; Nicol, C.J.; Vinson, C.; Gonzalez, F.J.; Reitman, M.L.
Title Liver peroxisome proliferator-activated receptor gamma contributes to hepatic steatosis, triglyceride clearance, and regulation of body fat mass Type Journal Article
Year 2003 Publication (up) The Journal of biological chemistry Abbreviated Journal J Biol Chem
Volume 278 Issue 36 Pages 34268-34276
Keywords Adipose Tissue/*metabolism; Animals; Blotting, Southern; Blotting, Western; Female; Hypoglycemia/genetics; Insulin Resistance/genetics; Lipid Metabolism; Liver/*metabolism; Liver Diseases/genetics/*metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; RNA/metabolism; Receptors, Cytoplasmic and Nuclear/*genetics/*physiology; Recombination, Genetic; Thiazoles/pharmacology; *Thiazolidinediones; Time Factors; Transcription Factors/*genetics/*physiology; Triglycerides/*metabolism
Abstract Peroxisome proliferator-activated receptor gamma (PPAR gamma) is a nuclear receptor that mediates the antidiabetic effects of thiazolidinediones. PPAR gamma is present in adipose tissue and becomes elevated in fatty livers, but the roles of specific tissues in thiazolidinedione actions are unclear. We studied the function of liver PPAR gamma in both lipoatrophic A-ZIP/F-1 (AZIP) and wild type mice. In AZIP mice, ablation of liver PPAR gamma reduced the hepatic steatosis but worsened the hyperlipidemia, triglyceride clearance, and muscle insulin resistance. Inactivation of AZIP liver PPAR gamma also abolished the hypoglycemic and hypolipidemic effects of rosiglitazone, demonstrating that, in the absence of adipose tissue, the liver is a primary and major site of thiazolidinedione action. In contrast, rosiglitazone remained effective in non-lipoatrophic mice lacking liver PPAR gamma, suggesting that adipose tissue is the major site of thiazolidinedione action in typical mice with adipose tissue. Interestingly, mice without liver PPAR gamma, but with adipose tissue, developed relative fat intolerance, increased adiposity, hyperlipidemia, and insulin resistance. Thus, liver PPAR gamma regulates triglyceride homeostasis, contributing to hepatic steatosis, but protecting other tissues from triglyceride accumulation and insulin resistance.
Address Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA. oksanag@bdg10.niddk.nih.gov
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0021-9258 ISBN Medium
Area Expedition Conference
Notes PMID:12805374 Approved no
Call Number refbase @ user @ Serial 81
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Author Etienne, A.S.; Maurer, R.; Seguinot, V.
Title Path integration in mammals and its interaction with visual landmarks Type Journal Article
Year 1996 Publication (up) The Journal of Experimental Biology Abbreviated Journal J Exp Biol
Volume 199 Issue Pt 1 Pages 201-209
Keywords Animals; Cognition/physiology; Cricetinae; Gerbillinae; Humans; Locomotion/*physiology; Mammals/*physiology; Mesocricetus; Mice; Proprioception/physiology; Rats; Visual Pathways/*physiology; Visual Perception/*physiology
Abstract During locomotion, mammals update their position with respect to a fixed point of reference, such as their point of departure, by processing inertial cues, proprioceptive feedback and stored motor commands generated during locomotion. This so-called path integration system (dead reckoning) allows the animal to return to its home, or to a familiar feeding place, even when external cues are absent or novel. However, without the use of external cues, the path integration process leads to rapid accumulation of errors involving both the direction and distance of the goal. Therefore, even nocturnal species such as hamsters and mice rely more on previously learned visual references than on the path integration system when the two types of information are in conflict. Recent studies investigate the extent to which path integration and familiar visual cues cooperate to optimize the navigational performance.
Address Laboratoire d'Ethologie, FPSE, Universite de Geneve, Carouge, Switzerland
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0022-0949 ISBN Medium
Area Expedition Conference
Notes PMID:8576691 Approved no
Call Number Equine Behaviour @ team @ Serial 2758
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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 (up) 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
Abstract
Address
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0022-3395 ISBN Medium
Area Expedition Conference
Notes PMID:5090972 Approved no
Call Number Equine Behaviour @ team @ Serial 2730
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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 (up) 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
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0022-3565 ISBN Medium
Area Expedition Conference
Notes PMID:15356214 Approved no
Call Number refbase @ user @ Serial 73
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Author Guo, G.L.; Moffit, J.S.; Nicol, C.J.; Ward, J.M.; Aleksunes, L.A.; Slitt, A.L.; Kliewer, S.A.; Manautou, J.E.; Gonzalez, F.J.
Title Enhanced acetaminophen toxicity by activation of the pregnane X receptor Type Journal Article
Year 2004 Publication (up) Toxicological sciences : an official journal of the Society of Toxicology Abbreviated Journal Toxicol Sci
Volume 82 Issue 2 Pages 374-380
Keywords Acetaminophen/pharmacokinetics/*toxicity; Analgesics, Non-Narcotic/pharmacokinetics/*toxicity; Animals; Aryl Hydrocarbon Hydroxylases/biosynthesis; Biotransformation; Blotting, Northern; Chromatography, High Pressure Liquid; Cytochrome P-450 CYP3A; Membrane Proteins; Mice; Mice, Knockout; Oxidoreductases, N-Demethylating/biosynthesis; Pregnenolone Carbonitrile/pharmacology; Receptors, Cytoplasmic and Nuclear/*drug effects; Receptors, Steroid/*drug effects; Sulfhydryl Compounds/metabolism
Abstract The pregnane X receptor (PXR) is a ligand-activated transcription factor and member of the nuclear receptor superfamily. Activation of PXR represents an important mechanism for the induction of cytochrome P450 3A (CYP3A) enzymes that can convert acetaminophen (APAP) to its toxic intermediate metabolite, N-acetyl-p-benzoquinone imine (NAPQI). Therefore, it was hypothesized that activation of PXR plays a major role in APAP-induced hepatotoxicity. Pretreatment with the PXR activator, pregnenolone 16alpha-carbonitrile (PCN), markedly enhanced APAP-induced hepatic injury, as revealed by increased serum ALT levels and hepatic centrilobular necrosis, in wild-type but not in PXR-null mice. Further analysis showed that following PCN treatment, PXR-null mice had lower CYP3A11 expression, decreased NAPQI formation, and increased maintenance of hepatic glutathione content compared to wild-type mice. Thus, these results suggest that PXR plays a critical role in APAP-induced hepatic toxicity, probably by inducing CYP3A11 expression and hence increasing bioactivation.
Address Laboratory of Metabolism, CCR, NCI, NIH, Bethesda, Maryland 20892, USA
Corporate Author Thesis
Publisher Place of Publication Editor
Language English Summary Language Original Title
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 1096-6080 ISBN Medium
Area Expedition Conference
Notes PMID:15456926 Approved no
Call Number refbase @ user @ Serial 71
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Author Rumiantsev, S.N.
Title [Biological function of Clostridium tetani toxin (ecological and evolutionary aspects)] Type Journal Article
Year 1973 Publication (up) Zhurnal Evoliutsionnoi Biokhimii i Fiziologii Abbreviated Journal Zh Evol Biokhim Fiziol
Volume 9 Issue 5 Pages 474-480
Keywords Animals; Cats; Chickens; Dogs; Ecology; Evolution; Goats; Guinea Pigs; Haplorhini; Horses; Insectivora; Mice; Perissodactyla; Rabbits; Rats; Sheep; *Tetanus Toxin
Abstract
Address
Corporate Author Thesis
Publisher Place of Publication Editor
Language Russian Summary Language Original Title K voprosu biologicheskoi funktsii toksina Clostridium tetani (ekologicheskie i evolutsionnye aspekty
Series Editor Series Title Abbreviated Series Title
Series Volume Series Issue Edition
ISSN 0044-4529 ISBN Medium
Area Expedition Conference
Notes PMID:4203684 Approved no
Call Number Equine Behaviour @ team @ Serial 2713
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