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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Impaired behavioral suppression by light in metabotropic glutamate receptor subtype 6-deficient mice.
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Impaired behavioral suppression by light in metabotropic glutamate receptor subtype 6-deficient mice.

机译:代谢型谷氨酸受体亚型6缺陷小鼠的光行为抑制受到损害。

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The metabotropic glutamate receptor subtype 6 is localized on the dendrites of ON bipolar cells in mammalian retina, and is responsible for synaptic transmission from photoreceptors to ON bipolar cells. We have previously provided electrophysiological evidence that metabotropic glutmate receptor subtype 6-deficient mice have an impairment in the ON visual pathway. In this study, we compared, between metabotropic glutamate receptor subtype 6-deficient (n=9) and wild-type mice (n=7), their daily wheel-running activity in constant dark and light-dark cycle environments. There was no difference in their free-running rhythmicity in a constant dark environment nor in their ability to entrain their active/rest phase to the phase-shifted light-dark cycle environment, indicating that the circadian system in mutant mice was functioning normally. However, the wheel-running activity was suppressed immediately after light onset of the light-dark cycle in wild-type mice (suppressive effect), whereas that of mutant mice was prolonged for several hours in spite of light onset (very weak suppressive effect). The suppression of activity in wild-type mice is a "masking effect" of the endogenous circadian rhythm in response to light stimuli.The results indicate that the failure of mutant mice to suppress their activity upon light onset is not due to abnormality in their circadian system, but to their lack of response to light stimuli. This study clearly demonstrates that the dysfunction of the ON visual pathway in metabotropic glutamate receptor subtype 6-deficient mice impairs their behavioral responsiveness to light and yet preserves their circadian system.
机译:代谢型谷氨酸受体亚型6位于哺乳动物视网膜中ON双极细胞的树突上,并负责从光感受器到ON双极细胞的突触传递。我们以前已经提供了电生理学证据,即代谢型谷氨酸受体亚型6缺陷型小鼠的ON视觉通路受损。在这项研究中,我们比较了代谢型谷氨酸受体亚型6缺陷(n = 9)和野生型小鼠(n = 7)在恒定的黑暗和光明-黑暗循环环境中每天的车轮行驶活动。在恒定的黑暗环境中,它们的自律性没有变化,也没有将它们的活动/休息阶段带入相移的明-暗循环环境的能力,这表明突变小鼠的昼夜节律系统功能正常。然而,在野生型小鼠中,在明暗周期的光发作后,车轮行驶活动立即受到抑制(抑制作用),而突变小鼠,尽管有光发作,其轮转活动仍被延长了几个小时(抑制作用非常弱)。 。野生型小鼠活动的抑制是内源性昼夜节律对光刺激的“掩盖效应”。结果表明,突变型小鼠在光发作时不能抑制其活动并不是由于其昼夜节律异常引起的。系统,但对光刺激缺乏反应。这项研究清楚地表明,代谢型谷氨酸受体亚型6缺陷型小鼠的ON视觉通路功能异常会损害其对光的行为反应能力,并保留其昼夜节律系统。

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