Literature DB >> 1249588

Spinal cord blood flow after acute experimental cord injury in dogs.

I R Griffiths.   

Abstract

Spinal cord blood flow (SCBF) was measured in dogs before and following acute injury with 300 or 500 g-cm force (GCF). In addition, the responses to high and low PaCO2 and low PaO2 levels were studied. The hydrogen clearance technique was used and 0.3 mm platinum electrodes were placed in grey matter, central white matter or peripheral white matter of the L2 segment. The pre-trauma flows were: grey matter 12.5 +/- 2.7; central white matter 14.4 +/- 3.6 and peripheral white matter 15.1 +/- 4.2 ml/100g/min. Following a 300 GCF injury, a marked and progressive reduction in SCBF occurred in the grey and central white matter. This was present for the subsequent 4 hr of the study. The flow was lower than pre-trauma values during the second hour in the grey matter (9.0 +/- 1.4) and the third hour in the central white matter (10.8 +/- 1.8). By the fifth hour after trauma the flow in the grey matter was 5.0 +/- 3.5 and in the central white matter 9.7 +/- 1.5. In the peripheral white matter the SCBF was 10 +/-3.7 during the third hour but subsequently the flow increased to 11.5 +/- 3.9. Paired t-tests showed that this still significantly lower than pre-trauma levels. Two dogs showed a hyperaemic response which was persistent in one case but only temporary in the other dog. The vasodilatatory effect of CO2 was lost after trauma and in some cases a steal phenomenon was present. The sensitivity to an increase in CO2 was 0.48 +/- 0.23 ml/100g/min Hg before injury and this decreased to 0.0075 +/- 0.137 during the second hour after injury. The vasodilatation to hypoxia (30-40 mm Hg) was also absent but the vasoconstrictor effect to low PaCO2 appeared better preserved. These findings also applied to the peripheral white matter where the SCBF was not significantly reduced. The results were similar but more pronounced after 500 GCF injury. The results show that following injury the central areas of the cord become rapidly and progressively ischaemic. The peripheral white matter does retain a reasonably normal flow depending on the magnitude of the impact force. However, the vessels in all these areas lose their ability to respond to normal physiological stimuli.

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Year:  1976        PMID: 1249588     DOI: 10.1016/0022-510x(76)90065-4

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  7 in total

1.  Comparison of cellular architecture, axonal growth, and blood vessel formation through cell-loaded polymer scaffolds in the transected rat spinal cord.

Authors:  Nicolas N Madigan; Bingkun K Chen; Andrew M Knight; Gemma E Rooney; Eva Sweeney; Lisa Kinnavane; Michael J Yaszemski; Peter Dockery; Timothy O'Brien; Siobhan S McMahon; Anthony J Windebank
Journal:  Tissue Eng Part A       Date:  2014-08-11       Impact factor: 3.845

2.  Early vascular changes in the spinal grey matter following impact injury.

Authors:  I R Griffiths; N Burns; A R Crawford
Journal:  Acta Neuropathol       Date:  1978-01-19       Impact factor: 17.088

Review 3.  Early microvascular reactions and blood-spinal cord barrier disruption are instrumental in pathophysiology of spinal cord injury and repair: novel therapeutic strategies including nanowired drug delivery to enhance neuroprotection.

Authors:  Hari Shanker Sharma
Journal:  J Neural Transm (Vienna)       Date:  2010-12-16       Impact factor: 3.575

4.  Membrane lipid changes in laminectomized and traumatized cat spinal cord.

Authors:  P Demediuk; R D Saunders; D K Anderson; E D Means; L A Horrocks
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

5.  Interstitial and tissue cations and electrical potential after experimental spinal cord injury.

Authors:  L Leybaert; G De Ley
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

6.  Vascular disruption and the role of angiogenic proteins after spinal cord injury.

Authors:  Michelle T L Ng; Anthea T Stammers; Brian K Kwon
Journal:  Transl Stroke Res       Date:  2011-10-13       Impact factor: 6.829

Review 7.  Rat models of spinal cord injury: from pathology to potential therapies.

Authors:  Jacob Kjell; Lars Olson
Journal:  Dis Model Mech       Date:  2016-10-01       Impact factor: 5.758

  7 in total

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