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Cresyl violet stained partial brain section of a Macaque. It is used in biology and medicine as a histological stain. Cresyl violet is an effective and reliable stain used for light microscopy sections. Initially, tissue sections are "defatted" by passing through graded dilutions of ethanol. Then, rehydrated by passing back through decreasing ...
Photomicrograph of Nissl bodies (two are indicated by arrows) in the cytoplasm of motor neurons in the anterior horn of the spinal cord; cresyl violet stain (purple) along with a luxol fast blue stain for myelin. Scale bar = 30 microns (0.03mm). Drawing of a motor neuron from the ventral horn of the medulla spinals of a rabbit.
These dyes intensely stain "Nissl bodies" (rough endoplasmic reticulum), which are abundant in neurons and reveal specific patterns of cytoarchitecture in the brain. Other common staining techniques used by histologists in other tissues (such as the hematoxylin and eosin or " H&E stain ") leave brain tissue appearing largely homogeneous and do ...
This is done by using various basic dyes (e.g. aniline, thionine, or cresyl violet) to stain the negatively charged RNA blue, and is used to highlight important structural features of neurons. The Nissl substance ( rough endoplasmic reticulum ) appears dark blue due to the staining of ribosomal RNA, giving the cytoplasm a mottled appearance.
The ligands cross the blood–brain barrier and attach to aggregated Aβ, and their retention in the brain is assessed by positron emission tomography. In addition, the presence of plaques and tangles can be estimated by measuring the amounts of the Aβ and tau proteins in the cerebrospinal fluid. [42] [43]
The hippocampal subfields are four subfields CA1, CA2, CA3, and CA4 that make up the structure of the hippocampus.Regions described in the hippocampus are the head, body, and tail, and other hippocampal subfields include the dentate gyrus, the presubiculum, and the subiculum.
The Schaffer collateral is located between the CA3 region and CA1 region in the hippocampus. Schaffer collaterals are the axons of pyramidal cells that connect two neurons (CA3 and CA1) and transfer information from CA3 to CA1. [5] [6] The entorhinal cortex sends the main input to the dentate gyrus (perforant pathway).
Low-threshold calcium spikes have been described in neurons from a variety of brain nuclei, including the thalamic relay, medial pontine reticular formation, lateral habenula, septum, deep cerebellar nuclei, CA1-CA3 of the hippocampus, association cortex, paraventricular and preoptic nuclei of the hypothalamus, dorsal raphe, globus pallidus ...