Rats were trained to switch-off aversive electrical brain stimulations applied to the periaqueductal gray (PAG) or mesencephalic locomotor region (MLR) by pressing a bar (switch-off behavior). We investigated the effects of IP injections of the benzodiazepine (BZ) receptor inverse agonist FG 7142 (2.5, 5, 10 mg/kg) or BZ receptor agonist chlordiazepoxide (CDP: 5 mg/kg) on the switch-off latency, i.e., the time elapsed between the onset of the stimulation and its offset by a press of the bar. It was found that FG 7142 decreased, whereas CDP increased the mean switch-off latency for electrical stimulation of the PAG, which is interpreted as a potentiating effect of FG 7142 and a reducing effect of CDP on the electrically induced aversive state. By contrast, neither FG 7142 nor CDP were found to affect the mean switch-off latency for MLR stimulations. These results suggest a difference in the pharmacological sensitivity to BZ receptor ligands between aversive states elicited by electrical stimulation of the PAG or MLR.
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http://dx.doi.org/10.1016/0091-3057(90)90340-n | DOI Listing |
Phys Med Biol
August 2019
Author to whom any correspondence should be addressed.
The step-and-shoot method of pencil beam scanning delivers the dose on a 3D grid in the target volume, with one dimension defined by the proton energy. While the dose per pencil beam may vary substantially within an iso-energy layer, the beam current typically remains constant. In this static operation mode, the inherent latency of the beam switch-off mechanism results in a lower limit for the deliverable spot dose, which may prevent the application of some of the low-weighted spots prescribed by the treatment planning system.
View Article and Find Full Text PDFIntegr Zool
September 2019
Department of Automation, Tsinghua University, Beijing, China.
Some shallow and middle optic tectum (OT) neurons have stable, asymmetric full-screen ON and OFF stimulus response properties, which makes them candidates for delay encoding. In this paper, we investigated the delay encoding mechanism for the neuronal clusters in the OT region of pigeons and determined the mechanism of delay coding in the OT region. By analyzing the responses of the neuron cluster under full-screen switch-on and switch-off stimulation, we found that the delay coding was widespread in the OT region where the ON/OFF stimulation time difference was 4-6 ms.
View Article and Find Full Text PDFNeuroscience
October 2016
Laboratory of Neuropsychopharmacology, FFCLRP, São Paulo University, Campus USP, Ribeirão Preto, São Paulo 14040-901, Brazil; Instituto de Neurociências e Comportamento, Avenida do Café, 2450, Ribeirão Preto, SP 14050-000, Brazil.
Recent discussions on the ethics in animal experimentation instigate the refinement of methods used in Behavioral Neuroscience, particularly regarding fear/anxiety paradigms. We propose the Light Switch-Off Test (LSOT), based on the innate motivation to cease an aversive stimulus (bright light), displayed naturally by rodents in their habitat. Forty-six male adult Wistar rats were allocated into independent groups: control, diazepam at 1 or 2mg/kg, and meta-Chlorophenylpiperazine (mCPP) at 0.
View Article and Find Full Text PDFJ Exp Biol
April 2010
UMR 1272 INRA-UPMC Physiologie de l'Insecte: Signalisation et Communication, F-78000 Versailles, France.
In the male moth, Agrotis ipsilon, mating induces a transient inhibition of behavioural and central nervous responses to sex pheromone. Newly mated males are not attracted to sex pheromone, and the sensitivity of their antennal lobe (AL) neurons is lower than in virgin males. This rapid transient olfactory inhibition prevents them from re-mating unsuccessfully until they have refilled their sex glands.
View Article and Find Full Text PDFExp Gerontol
April 2006
Department of Carcinogenesis and Oncogerontology, N.N.Petrov Research Institute of Oncology, Pesochny-2, St Petersburg 197758, Russian Federation.
Studies in mammals have led to the suggestion that hyperglycemia and hyperinsulinemia are important factors both in aging and in the development of cancer. Insulin/insulin-like growth factor 1 (IGF-1) signaling molecules that have been linked to longevity include DAF-2 and InR and their homologues in mammals, and inactivation of the corresponding genes is followed by increased life span in nematodes, fruit flies and mice. It is possible that the life-prolonging effects of calorie restriction are due to decreasing IGF-1 levels.
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