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Growth --- Cattle --- Regulation endocrine
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Aggression. --- Endocrine system. --- Endocrine. --- Male rat. --- Male. --- Rat.
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Behavior. --- Development. --- Endocrine. --- Gerbil. --- Gerbils. --- Morphology. --- Time.
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Cattle --- monoclonal antibodies --- animal growth promoters --- Immune response --- Endocrine glands
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Abnormal behaviour. --- Animal welfare. --- Animal-welfare. --- Animal. --- Diseases. --- Endocrine system. --- Environment. --- Physiological. --- Pig. --- Stereotypy. --- Stress. --- Welfare.
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N
Aggression. --- Aggressive. --- Behaviour. --- Dba/2j. --- Dominance hierarchies. --- Dominance. --- Endocrine. --- Enrichment. --- Environmental enrichment. --- Hierarchy. --- Male.
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2 inbred strains. --- Activation. --- Aggression. --- Cage design. --- Cage. --- Consequences. --- Design. --- Endocrine. --- Inbred strains. --- Laboratory. --- Male. --- Mouse. --- Social-organization.
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Abstract Our aim was to study the role of the olfactory amygdala (medial and cortical nuclei) and the ventromedial nucleus of the hypothalamus (VMN) in the ability of the male odour or live males to induce a release of luteinizing hormone in anoestrus ewes. To achieve this, we temporarily blocked the activity of these structures by localized retrodialysis administration of the anaesthetic lidocaine. The effect of ram odour on the secretion of luteinizing hormone was completely blocked by inactivation of the cortical nucleus of the amygdala. In contrast, inactivation of part of the accessory olfactory system (the medial nucleus of the amygdala or the VMN) had no effect. In the presence of the male, lidocaine never impaired the endocrine response of the ewes. These results show that modulation of reproduction by the sexual partner even through pheromonal cues does not occur via the direct circuit of the accessory system. On the contrary, the cortical nucleus of the amygdala is absolutely necessary for the treatment of and/or the response to the male olfactory signal but this structure can be bypassed when other sensory cues are available
Ability. --- Activity. --- Amygdala. --- Cues. --- Endocrine. --- Ewe. --- Ewes. --- Hormone. --- Hypothalamus. --- Luteinizing-hormone. --- Male. --- Males. --- Modulation. --- Nucleus. --- Odour. --- Olfactory. --- Ram. --- Release. --- Reproduction. --- Response. --- Secretion. --- Sensory. --- Sexual. --- System. --- Treatment.
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Melatonin, a hormone produced in the pineal gland and released into the general circulation on a diurnal basis, has been implicated in many behavioral processes, where it has been shown to have anxiolytic, sedative, and anticonvulsant effects. Male gerbils (Meriones unguiculatus) injected daily with melatonin (25 mu g, s,c.) exhibited a reduced seizure response to pentylenetetrazol (PTZ, 60 mg/kg, s.c.). The present studies determined 1) whether melatonin's effect was related to the time of day that it was administered and 2) whether a single acute injection of melatonin at various doses could produce anticonvulsant activity. Gerbils provided with 13 weeks of daily melatonin injections (25 mu g, s.c,) exhibited fewer convulsions after PTZ treatment irrespective of the time of day melatonin was injected. In addition, the melatonin-treated gerbils had lower mortality rates (1/12) than the untreated or vehicle-injected gerbils (5/12). On the other hand, single acute injections of melatonin (0.1-10 mg/kg, i.p,) produced no anticonvulsant activity. It appears that the anticonvulsant effects of melatonin occur only after the animals are chronically exposed to the indole. In addition, melatonin's anticonvulsant ability may utilize a different mechanism than those involved in its endocrine effects, since no diurnal difference in melatonin's anticonvulsant activity was observed
Ability. --- Activity. --- Animal. --- Animals. --- Anxiolytic activity. --- Boxes. --- Brain. --- Endocrine. --- Epilepsy. --- Gerbil. --- Gerbils. --- Gland. --- Hormone. --- Human. --- Implants. --- Induced gonadal regression. --- Injections. --- Male. --- Melatonin. --- Meriones unguiculatus. --- Meriones-unguiculatus. --- Mice. --- Mortality. --- Mouse. --- Pentylenetetrazol. --- Pineal. --- Response. --- Seizure. --- Seizures. --- Sleep. --- Time. --- Treatment. --- Unguiculatus.
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