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Artifactual dendritic beading in rat spinal cord induced by perfusion with cold saline and paraformaldehyde

  • Shu Xin Zhang
  • , Eric G. Holmberg
  • , James W. Geddes

Producción científica: Articlerevisión exhaustiva

6 Citas (Scopus)

Resumen

Extensive dendritic beading of MAP2 (microtubule-associated protein 2) immunoreactivity has previously been observed in the contused rat spinal cord. However, we have also observed dendritic beading in occasional uninjured animals. The purpose of this study was to examine the possibility that perfusion conditions contributed to the dendritic beading. Under deep anesthesia, uninjured rats (adult female Long-Evans, 200-225 g) were transcardially perfused with 0.9% saline solution followed by 4% paraformaldehyde at cold (4 °C) or warm (20 °C) temperature, and at a low (20 ml/min) or high (50 ml/min) flow rate. Dendrites were visualized by MAP2 immunoreactivity. The results demonstrate that perfusion with cold solutions at a high flow rate induces pronounced dendritic beading, and when perfused at a low flow rate, results in moderate dendritic beading. Warm perfusates did not induce dendritic beading when administered at a low flow rate, but occasional beading was observed with a high flow rate. Western blots revealed spectrin breakdown, but not MAP2 loss, in rats perfused with cold saline solution at a high flow rate, conditions that also resulted in dendritic beading. These findings demonstrate that dendritic morphology is sensitive to both temperature and flow rate of the perfusate. Warm fixative and a low perfusion flow rate minimized the perfusion-induced dendritic beading.

Idioma originalEnglish
Páginas (desde-hasta)38-43
Número de páginas6
PublicaciónJournal of Neuroscience Methods
Volumen163
N.º1
DOI
EstadoPublished - jun 15 2007

Nota bibliográfica

Funding Information:
The authors are grateful to Fengfa Huang for excellent technical assistance. This study was supported by Paralysis Project of America grant (SXZ), Kentucky Spinal Cord and Head Injury Research Trust grant GA-9601-K (JWG), NIH RO1 NS045726 (JWG), and Spinal Cord Society USA.

Financiación

The authors are grateful to Fengfa Huang for excellent technical assistance. This study was supported by Paralysis Project of America grant (SXZ), Kentucky Spinal Cord and Head Injury Research Trust grant GA-9601-K (JWG), NIH RO1 NS045726 (JWG), and Spinal Cord Society USA.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilR01NS045726
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke Council
Paralysis Project of America
International Spinal Cord Society
Kentucky Spinal Cord and Head Injury Research TrustGA-9601-K
Kentucky Spinal Cord and Head Injury Research Trust

    ASJC Scopus subject areas

    • General Neuroscience

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