2016
DOI: 10.1007/s11055-016-0228-7
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Changes in the Number of Neurons in the Rat Motor Cortex and Movement Activity with Age

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Cited by 9 publications
(4 citation statements)
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“…Paraffin embedded sections of 5 μm thickness are prepared F I G U R E 2 Schematic presentation of respiratory and cardiac cessation. After placement in the stereotaxic apparatus the animal was administrated with drugs that caused immediate respiratory arrest (propofol followed by cisatracurium) or acute cardiac cessation (lidocaine solution) with Microm HM 450 microtome (Microm International GmbH, Germany) stained with HE by standard protocols [25] and with our own patented Nissl staining and silver impregnation combined method [26]. This new approach allows to see both silver impregnated and cresyl violet stained neurons with different structural and functional properties.…”
Section: Methodsmentioning
confidence: 99%
“…Paraffin embedded sections of 5 μm thickness are prepared F I G U R E 2 Schematic presentation of respiratory and cardiac cessation. After placement in the stereotaxic apparatus the animal was administrated with drugs that caused immediate respiratory arrest (propofol followed by cisatracurium) or acute cardiac cessation (lidocaine solution) with Microm HM 450 microtome (Microm International GmbH, Germany) stained with HE by standard protocols [25] and with our own patented Nissl staining and silver impregnation combined method [26]. This new approach allows to see both silver impregnated and cresyl violet stained neurons with different structural and functional properties.…”
Section: Methodsmentioning
confidence: 99%
“…Organ samples were fixed in Carnoy's fluid and embedded in paraffin. 5 μm-thick sections were stained with 1% cresyl violet aqueous solution with acetate buffer (56 C) for 20 min (for brain sections), and the other organs' specimen were stained with hematoxylin and eosin by standard methods [23].…”
Section: Morphological Studies Of Organs and Tissuesmentioning
confidence: 99%
“…Выполняли фиксацию кусочков мозга в жидкости Карнуа с последующей заливкой в парафин. Получали срезы толщиной 5 микрометров, которые в дальнейшем окрашивали 1% раствором водного крезилвиолета на ацетатном буфере в термостате (56°С) в течение 20 мин, а также гематоксилином и эозином по стандартным методикам [10], после чего просветляли и накрывали покровными стеклами.…”
Section: морфологическое исследование коры головного мозгаunclassified