Myometrial Responses to Beta-Adrenoceptor Antagonists in Gynecological Malignancies.
Adrenergic beta-Agonists
/ metabolism
Adrenergic beta-Antagonists
/ pharmacology
Bupranolol
/ pharmacology
Endometrial Neoplasms
/ physiopathology
Ethanolamines
/ metabolism
Female
Genital Neoplasms, Female
/ physiopathology
Humans
Myometrium
/ drug effects
Ovarian Neoplasms
/ physiopathology
Propanolamines
/ pharmacology
Propranolol
/ pharmacology
Prospective Studies
Uterine Cervical Neoplasms
/ physiopathology
Uterine Contraction
/ drug effects
Uterus
Beta-adrenoceptor
Cervical cancer
Endometrial cancer
Ovarian cancer
Uterine contractions
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
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
162-169Informations de copyright
© 2021 S. Karger AG, Basel.