Myometrial Responses to Beta-Adrenoceptor Antagonists in Gynecological Malignancies.


Journal

Gynecologic and obstetric investigation
ISSN: 1423-002X
Titre abrégé: Gynecol Obstet Invest
Pays: Switzerland
ID NLM: 7900587

Informations de publication

Date de publication:
2021
Historique:
received: 23 07 2020
accepted: 11 12 2020
pubmed: 1 3 2021
medline: 29 6 2021
entrez: 28 2 2021
Statut: ppublish

Résumé

The aim of the study was to determine the influence of beta-adrenoceptor (ADRB) antagonists on contractile activity of the nonpregnant human uterus in patients affected by gynecological malignancies. This was a controlled and prospective ex vivo study. The work was conducted as a collaboration between 4 academic departments. Myometrial specimens were obtained from women undergoing hysterectomy for benign gynecological disorders (reference group; N = 15), and ovarian (N = 15), endometrial (N = 15), synchronous ovarian-endometrial (N = 3), and cervical cancer (N = 10). Contractions of myometrial strips in an organ bath before and after applications of ADRB antagonists (propranolol, bupranolol, SR 59230A, and butoxamine) were studied under isometric conditions. Propranolol and bupranolol attenuated contractions in the endometrial and cervical cancer groups similar to that in the reference group (all p < 0.05), whereas opposite effects were observed in the ovarian and synchronous ovarian-endometrial cancer groups. SR 59230A and butoxamine significantly increased contractions in the ovarian cancer group (both p < 0.001). These results require now to be placed into a firm clinical context. Our study indicates that ovarian cancer considerably alters contractile activity of the nonpregnant human uterus in response to ADRB antagonists. This suggests a pathogenetic role of beta-adrenergic pathways in this malignancy. Furthermore, propranolol and bupranolol substantially influence spontaneous uterine contractility.

Identifiants

pubmed: 33640886
pii: 000513718
doi: 10.1159/000513718
doi:

Substances chimiques

3-(2-ethylphenoxy)-1-(1,2,3,4-tetrahydronaphth-1-ylamino)-2-propanol oxalate 0
Adrenergic beta-Agonists 0
Adrenergic beta-Antagonists 0
Ethanolamines 0
Propanolamines 0
Bupranolol 858YGI5PIT
Propranolol 9Y8NXQ24VQ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

162-169

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Beata Modzelewska (B)

Department of Biophysics, Medical University of Białystok, Białystok, Poland.

Marcin Jóźwik (M)

Department of Gynecology and Obstetrics, Faculty of Medicine, Collegium Medicum, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland.

Tomasz Kleszczewski (T)

Department of Biophysics, Medical University of Białystok, Białystok, Poland.

Stanisław Sulkowski (S)

Department of General Pathomorphology, Medical University of Białystok, Białystok, Poland.

Maciej Jóźwik (M)

Department of Gynecology and Gynecologic Oncology, Medical University of Białystok, Białystok, Poland, jozwikmc@interia.pl.

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Classifications MeSH