Atherosclerosis
Volume 170, Issue 1 , Pages 141-146, September 2003

Remodelling of cerebrospinal fluid lipoproteins after subarachnoid hemorrhage

  • A.D. Kay

      Affiliations

    • Department of Neurosurgery, University of Glasgow, Institute of Neurological Sciences, Southern General Hospital, Glasgow G51 4TF, UK
    • Corresponding Author InformationCorresponding author. Tel.: +44-141-201-1100; fax: +44-141-201-2998
  • ,
  • S.P. Day

      Affiliations

    • Department of Pathological Biochemistry, University of Glasgow, 4th Floor Queen Elizabeth building Glasgow Royal Infirmary, 10 Alexandra Parade, Glasgow G31 2ER, UK
    • Tel.: +44-141-211-4979; fax: +44-141-553-2558.
  • ,
  • J.A.R. Nicoll

      Affiliations

    • Division of Clinical Neurosciences (formerly department of Neuropathology, University of Glasgow), University of Southampton, Southampton General Hospital, Southampton SO16 6YD, UK
    • Tel.: +44-2380-79-6634; fax: +44-2380-79-6839.
  • ,
  • C.J. Packard

      Affiliations

    • Department of Pathological Biochemistry, University of Glasgow, 4th Floor Queen Elizabeth building Glasgow Royal Infirmary, 10 Alexandra Parade, Glasgow G31 2ER, UK
    • Tel.: +44-141-211-4979; fax: +44-141-553-2558.
  • ,
  • M.J. Caslake

      Affiliations

    • Department of Pathological Biochemistry, University of Glasgow, 4th Floor Queen Elizabeth building Glasgow Royal Infirmary, 10 Alexandra Parade, Glasgow G31 2ER, UK
    • Tel.: +44-141-211-4979; fax: +44-141-553-2558.

Received 20 November 2002; received in revised form 4 June 2003; accepted 11 June 2003.

Abstract 

Lipoprotein particles (Lps) in normal human cerebrospinal fluid (CSF) are distinct from those found in plasma and include unique apolipoprotein E (apoE indicates protein; APOE, gene) containing lipoproteins rarely seen in human plasma. Less favourable neurological recovery after subarachnoid hemorrhage (SAH) has been observed in patients who posses the APOE ε4 allele raising the possibility that apoE influences neuronal survival after brain injury. We analysed Lps from control and SAH CSF testing the hypotheses that following brain injury CSF Lps undergo remodelling and apoE containing Lps are selectively depleted from brain injury CSF. Lipoproteins were fractionated using CSF from six control pools and six patients with SAH on a sepharose 6HR 10/30 size exclusion column. Fractions were assayed for total cholesterol (TC), free cholesterol (FC), phospholipid, triglyceride (TG), apoE, apolipoprotein B (apoB), and apolipoprotein AI (apoAI). Compared to control CSF there were significant (P<0.05) increases in TC, FC, TG, and apoAI in SAH CSF. Plasma sized apoB-containing lipoproteins and a very small apoAI-containing Lps were identified in the SAH CSF, which were not present in controls. However, despite the release of plasma lipoproteins into the subarachnoid space, there was no significant increase in CSF apoE. These data provide novel indirect evidence suggesting that after SAH CSF Lps undergo remodelling and apoE containing Lps are selectively reduced in brain injury CSF. The remodelling of CSF Lps and selective reduction of apoE containing lipoproteins may reflect an important response of the human brain to injury.

Keywords: Cerebrospinal fluid, Lipoproteins, Subarachnoid hemorrhage, Brain injury

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PII: S0021-9150(03)00249-1

doi:10.1016/S0021-9150(03)00249-1

Atherosclerosis
Volume 170, Issue 1 , Pages 141-146, September 2003