Determining factors for optimal neuronal and glial Golgi-Cox staining.

Golgi staining allows for the analysis of neuronal arborisations and connections and is considered a powerful tool in basic and clinical neuroscience. The fundamental rules for improving neuronal staining using the Golgi-Cox method are not fully understood; both intrinsic and extrinsic factors may c...

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Published in:Histochemistry & Cell Biology Vol. 154; no. 4; pp. 431 - 449
Main Authors: Narayanan, Sareesh Naduvil, Bairy, Laxminarayana Kurady, Srinivasamurthy, Suresh Kumar
Format: Journal Article
Published: Springer Nature Oct2020
Online Access:View this record in EBSCOhost
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      dt: Oct2020
      vid: 154
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00418-020-01891-9
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        atl: Determining factors for optimal neuronal and glial Golgi-Cox staining.
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        au:
          Narayanan, Sareesh Naduvil
          Bairy, Laxminarayana Kurady
          Srinivasamurthy, Suresh Kumar
        affil: Department of Physiology, RAK College of Medical Sciences, RAK Medical and Health Sciences University, PO Box 11172, Ras Al Khaimah, United Arab Emirates
      sug:
      ab: Golgi staining allows for the analysis of neuronal arborisations and connections and is considered a powerful tool in basic and clinical neuroscience. The fundamental rules for improving neuronal staining using the Golgi-Cox method are not fully understood; both intrinsic and extrinsic factors may control the staining process. Therefore, various conditions were tested to improve the Golgi-Cox protocol for vibratome-cut rat brain sections. Optimal staining of cortical neurons was achieved after 72 h of impregnation. Well-stained neurons in both cortical and subcortical structures were observed after 96 h of impregnation. The dendritic arborisation pattern of cortical neurons derived from the 72-h impregnation group was comparable to those of the 96 and 168-h impregnation groups. The entire brain was stained well when the pH of the Golgi-Cox solution was 6.5 and that of the sodium carbonate solution was 11.2. Lack of brain perfusion or perfusion with 0.9% NaCl did not influence optimal neuronal staining. Perfusion with 37% formaldehyde, followed by impregnation, only resulted in glial staining, but perfusion with 4% formaldehyde facilitated both glial and neuronal staining. Whole brains required longer impregnation times for better staining. Although every factor had a role in determining optimal neuronal staining, impregnation time and the pH of staining solutions were key factors among them. This modified Golgi-Cox protocol provides a simple and economical procedure to stain both neurons and glia separately.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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