Psychopharmacology

, Volume 180, Issue 4, pp 595–606 | Cite as

GABA-benzodiazepine receptor function in alcohol dependence: a combined 11C-flumazenil PET and pharmacodynamic study

  • A. R. Lingford-Hughes
  • S. J. Wilson
  • V. J. Cunningham
  • A. Feeney
  • B. Stevenson
  • D. J. Brooks
  • D. J. Nutt
Original Investigation

Abstract

Rationale

Gamma-aminobutyric acid (GABA)-benzodiazepine receptor function is hypothesised to be reduced in alcohol dependence.

Objectives

We used positron emission tomography (PET) with [11C]flumazenil, a non-selective tracer for brain GABA-benzodiazepine (GABA-BDZ) receptor binding, to determine in vivo the relationship between BDZ receptor occupancy by an agonist, midazolam, and its functional effects.

Methods

Abstinent male alcohol dependent subjects underwent [11C]flumazenil PET to measure occupancy of BDZ receptors by midazolam whilst recording its pharmacodynamic effects on behavioural and physiological measures. Rate constants describing the exchange of [11C]flumazenil between the plasma and brain compartments were derived from time activity curves.

Results

A 50% reduction in electroencephalography (EEG)-measured sleep time was seen in the alcohol dependent group despite the same degree of occupancy by midazolam as seen in the control group. The effects of midazolam on other measures of benzodiazepine receptor function, increasing EEG beta1 power and slowing of saccadic eye movements, were similar in the two groups. No differences in midazolam or flumazenil metabolism were found between the groups.

Conclusions

In summary, our study suggests that alcohol dependence in man is associated with a reduced EEG sleep response to the benzodiazepine agonist, midazolam, which is not explained by reduced BDZ receptor occupancy, and is consistent with reduced sensitivity in this measure of GABA-BDZ receptor function in alcohol dependence. The lack of change in other functional measures may reflect a differential involvement of particular subtypes of the GABA-BDZ receptor.

Keywords

PET Flumazenil Alcoholism GABA-benzodiazepine receptor EEG Saccadic eye movements 

Notes

Acknowledgements

We are grateful to Dr. Mike Franklin, Oxford for measurement of midazolam, all staff at Hammersmith Imanet Ltd. (formerly MRC Cyclotron Unit) but particularly Safiye Osman, Jo Holmes, and Andy Blythe, Mr. Lindsay Taylor, University of Bristol and all staff and patients at the Robert Smith Unit, Bristol and ACAD, Weston-super-Mare. This study was funded by an MRC Programme Grant, G9515859.

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Copyright information

© Springer-Verlag 2005

Authors and Affiliations

  • A. R. Lingford-Hughes
    • 1
    • 2
  • S. J. Wilson
    • 1
  • V. J. Cunningham
    • 3
  • A. Feeney
    • 1
    • 2
  • B. Stevenson
    • 1
    • 2
    • 4
  • D. J. Brooks
    • 2
    • 3
  • D. J. Nutt
    • 1
  1. 1.Psychopharmacology UnitUniversity of BristolBristolUK
  2. 2.MRC Clinical Sciences Centre and Division of Neuroscience, Faculty of MedicineImperial College School of MedicineLondonUK
  3. 3.Hammersmith Imanet Ltd.Hammersmith HospitalLondonUK
  4. 4.Community Drug TeamPaget HouseLeicesterUK

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