Skip to main content
Log in

Plasma chlorpropamide: A critical factor in chlorpropamide-alcohol flush

  • Originals
  • Published:
European Journal of Clinical Pharmacology Aims and scope Submit manuscript

Summary

The chlorpropamide-alcohol flush (CPAF) phenomenon was quantitatively related to blood levels of acetaldehyde and chlorpropamide in 105 Type II diabetics, of whom 74 had not previously taken the drug and 31 were on chronic treatment. Standardized skin temperature recordings were made with a sensitive probe. Plasma ethanol and acetaldehyde concentrations were determined by gas chromatography, and those of chlorpropamide by high-pressure liquid chromatography. There were significant positive correlations between plasma acetaldehyde and the skin temperature increase, between plasma chlorpropamide and plasma acetaldehyde, and between plasma chlorpropamide and the skin temperature increase. CPAF-positive patients became CPAF-negative and vice versa following reduction and increase, respectively, in the dose of chlorpropamide. Thus, the CPAF reaction is a consequence of chlorpropamide inhibition of the oxidation of ethanol-generated acetaldehyde, and it appears that the plasma concentration of chlorpropamide is critical. It remains an open question whether the CPAF test has any prognostic value.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Leslie RDG, Pyke DA (1978) Chlorpropamide-alcohol flushing: a dominantly inherited trait associated with diabetes. Br Med J 2: 1519–1521

    Google Scholar 

  2. Leslie RDG, Barnett AH, Pyke DA (1979) Diabetic retinopathy and chlorpropamide alcohol flushing. Lancet 1: 997–999

    Google Scholar 

  3. Barnett AH, Pyke DA (1980) Chlorpropamide-alcohol flushing and large-vessel disease in non-insulin-dependent diabetes. Br Med J 1: 261–262

    Google Scholar 

  4. Jerntorp P, Almér L-O (1981) Chlorpropamide-alcohol flushing in relation to macro-angiopathy and peripheral neuropathy in non-insulin dependent diabetes. Acta Med Scand [Suppl] 656: 33–36

    Google Scholar 

  5. Barnett AH, Leslie RDG, Pyke DA (1981) Chlorpropamide-alcohol flushing and proteinuria in non-insulin-dependent diabetics. Br Med J 1: 522–523

    Google Scholar 

  6. Köbberling J, Bengsch N, Brüggeboes B, Schwarck H, Tillil H, Weber M (1980) The chlorpropamide alcohol flush — lack of specificity for familial non-insulin dependent diabetes. Diabetologia 19: 359–363

    Google Scholar 

  7. De Silva NE, Tunbridge WMG, Alberti KGMM (1981) Low incidence of chlorpropamide-alcohol flushing in diet-treated, non-insulin-dependent diabetes. Lancet 1: 128–131

    Google Scholar 

  8. Jerntorp P, Almér L-O, Melander A (1981) Is the blood chlorpropamide critical in chlorpropamide alcohol flush? Lancet 1: 165–166

    Google Scholar 

  9. Podgainy H, Bressler R (1968) Biochemical basis of the sulfonylurea-induced Antabuse syndrome. Diabetes 17: 679–683

    Google Scholar 

  10. Jerntorp P, Öhlin H, Bergström B, Almér L-O (1981) Increase in plasma acetaldehyde; an objective indicator of the chlorpropamide alcohol flush. Diabetes 30: 788–791

    Google Scholar 

  11. Wåhlin-Boll E, Melander A (1979) High-performance liquid chromatographic determination of glipizide and some other sulfonylurea drugs in serum. J Chromatogr 164: 541–546

    Google Scholar 

  12. Stowell AR (1979) An improved method for the determination of acetaldehyde in human blood with minimal ethanol interference. Clin Chim Acta 98: 201–205

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jerntorp, P., Almér, L.O., Öhlin, H. et al. Plasma chlorpropamide: A critical factor in chlorpropamide-alcohol flush. Eur J Clin Pharmacol 24, 237–242 (1983). https://doi.org/10.1007/BF00613824

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00613824

Key words

Navigation