4.7 Article

Dinitrosyl iron complexes with glutathione suppress experimental endometriosis in rats

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 727, Issue -, Pages 140-147

Publisher

ELSEVIER
DOI: 10.1016/j.ejphar.2014.01.002

Keywords

Endometriosis; Dinitrosyl iron complexes; Nitric oxide

Funding

  1. RAS Presidium Program Basic Science for Medicine
  2. Russian Foundation for Basic Research [12-04-00346a]

Ask authors/readers for more resources

Dinitrosyl iron complexes (DNIC) with glutathione exert a cytotoxic effect on endometrioid tumours in rats with surgically induced experimental endometriosis. Intraperitoneal treatment of rats (Group 1) with DNIC (12.5 mu moles/kg, daily, for 12 days), beginning with day 4 after the surgical operation (implantation of two 2 mm thick uterine fragments onto the abdominal wall) followed by 14 day keeping of animals on a standard feeding schedule (without medication) resulted in complete inhibition of the growth of endometrioid implants (EMI) in the majority of experimental animals. The ratio of mean EMI volumes in control and experimental Ears of Group 1 was 14:1. In Group 2 rats, the use of a similar treatment protocol 4 weeks after surgery changed this ratio to 14:1. Noteworthy, the decrease of this ratio was irrelevant to deceleration of EMI growth at later periods after surgery. The histopathological analysis of EMl samples from experimental rats of Group 2 demonstrated complete disappearance of endometrial cysts suggesting a cytotoxic effect of DNIC on the rumours. The data obtained demonstrate that DNIC with gluthathione and, probably, with other thiol-containing ligands hold considerable promise in the design of drugs for treating endometriosis in female patients. (C) 2014 Elsevier B.V. All rights reserved

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available