Reduction of beta-adrenergic receptors can explain the lack of rebound effect after tertatolol withdrawal

A. De Blasi, B. P L Pittana, C. M. Fratelli, S. Garattini

Research output: Contribution to journalArticlepeer-review

Abstract

Tertatolol is a potent beta-blocker with no intrinsic sympathomimetic activity (ISA) or β12 receptor subtype selectivity. We provide evidence that tertatolol competitively inhibits ß-adrenergic receptors (ß-AR) and induces a marked and persistent reduction of their number. This has been consistently found in vitro and in vivo. The in vitro study showed that the receptor reduction by tertatolol was rapid (about 1 h at 37°C) slowly reversible and independent of ISA. This effect was also observed in vivo. In healthy volunteers, seven days tertatolol treatment lowered the number of β-AR by 26%.This number gradually rose back to the pretreatment levels, and a significant effect was still present on day 3 after drug withdrawal. The redu tion of heart rate by tertatolol was also persistent and was still significant on day 3 to 5 after drug withdrawal. We conclude that the reduction of tin receptor numbers may be important in producing lack of a rebound effect after discontinuation of chronic tertatolol treatment. Am J Hypertens 1982;2:257S - 260S.

Original languageEnglish
Pages (from-to)257s-260s
JournalAmerican Journal of Hypertension
Volume2
Issue number11
DOIs
Publication statusPublished - 1989

Keywords

  • Human β-adrenoceptors
  • Tertatolol
  • β-adrenergic blocking therapy

ASJC Scopus subject areas

  • Internal Medicine
  • Cardiology and Cardiovascular Medicine

Fingerprint Dive into the research topics of 'Reduction of beta-adrenergic receptors can explain the lack of rebound effect after tertatolol withdrawal'. Together they form a unique fingerprint.

Cite this