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Tissue functions mediated by beta(3)-adrenoceptors-findings and challenges

  • Martin C. Michel
  • , Peter Ochodnicky
  • , Roger J. Summers

Research output: Contribution to journalEditorialAcademicpeer-review

Abstract

As beta(3)-adrenoceptor agonists metamorphose from experimental tools into therapeutic drugs, it is vital to obtain a comprehensive picture of the cell and tissue functions mediated by this receptor subtype in humans. Human tissues with proven functions and/or a high expression of beta(3)-adrenoceptors include the urinary bladder, the gall bladder, and other parts of the gastrointestinal tract. While several other beta(3)-adrenoceptor functions have been proposed based on results obtained in animals, their relevance to humans remains uncertain. For instance, beta(3)-adrenoceptors perform an important role in thermogenesis and lipolysis in rodent brown and white adipose tissue, respectively, but their role in humans appears less significant. Moreover, the use of tools such as the agonist BRL 37344 and the antagonist SR59230A to demonstrate functional involvement of beta(3)-adrenoceptors may lead in many cases to misleading conclusions as they can also interact with other beta-adrenoceptor subtypes or even non-adrenoceptor targets. In conclusion, we propose that many responses attributed to beta(3)-adrenoceptor stimulation may need re-evaluation in the light of the development of more selective tools. Moreover, findings in experimental animals need to be extended to humans in order to better understand the potential additional indications and side effects of the beta(3)-adrenoceptor agonists that are beginning to enter clinical medicine
Original languageEnglish
Pages (from-to)103-108
JournalNaunyn-Schmiedeberg s archives of pharmacology
Volume382
Issue number2
DOIs
Publication statusPublished - 2010

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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