Tamoxifen protects against obesity-related metabolic disorders

Tamoxifen protects against obesity-related metabolic disorders
Body weight evolution (A) and food intake (B) were recorded weekly. C: Body composition (fat mass) was assessed by magnetic resonance imaging (EchoMRI) after 12 weeks of HFD. D: i.p. glucose tolerance tests were performed after 6 weeks of HFD. E: Insulin resistance was estimated by homeostatic model assessment of insulin resistance (HOMA-IR) score, calculated after 12 weeks of HFD. F: Intrahepatic neutral lipid content and liver histology were assessed at sacrifice. Representative images of hematoxylin and eosin (H&E) and Oil Red O (ORO) staining on liver sections. Insets show higher magnification. Data are expressed as means ± SEM. *P < 0.05, **P < 0.01, and ***P < 0.001. Scale bars: 100 mm (Liver Histology); 50 μm (G, insets). Original magnification, ×40 (insets). VEH-Vehicle alone; TAM-Tamoxifen treated. Credit: The American Journal of Pathology

Tamoxifen, a selective estrogen receptor modulator, is the gold standard for endocrine treatment of estrogen-receptor positive breast cancer. Tamoxifen is also known to have metabolic effects. A new study in The American Journal of Pathology reports that the drug also prevents obesity, fatty liver, and insulin resistance in female mice who were fed a high-fat diet and whose ovaries had been removed. The study was also able to pinpoint which estrogen receptors underlie these protective effects, opening up possibilities for new therapies to treat these conditions.

"For the past two decades, estrogen receptor α (ERα) has been identified as a key regulator of energy and glucose homeostasis and consequently proposed as a promising target to develop new therapeutic strategies to fight against obesity-related metabolic disorders, such as type 2 diabetes and nonalcoholic fatty liver disease. However, understanding the mechanisms of the metabolic protection conferred by ERα activation has been a crucial challenge," explained Pierre Gourdy, MD, PhD, INSERM UMR1048, Institut des Maladies Métaboliques et Cardiovasculaires, Université de Toulouse (France).

Mice whose ovaries had been removed were fed a high-fat diet and treated with either or a placebo for 12 weeks. Investigators found that tamoxifen prevented weight gain, which was attributed to a significant reduction in food intake compared with controls. Tamoxifen-treated were less likely to develop glucose intolerance, insulin resistance, as well as deposits of fat in the liver.

The researchers knew that ERα exerts its effects through two activation functions known as ERα-AF1 and ERα-AF2, directly involved in the transcriptional regulation of gene expression. Tamoxifen acts as an ERα-AF1 agonist or an ERα-AF2 antagonist according to its tissue/organ targets. To better understand the molecular mechanisms underlying tamoxifen's metabolic effects, the scientists treated mice genetically bred to be deficient either for the entire ER-α (ERα-/-) or just ERα-AF1 (AF1-/-°) with either tamoxifen or placebo and compared the results to wild-type mice (ERα+/+ or AF1+/+) that underwent similar treatment. All the mice were fed a high-fat diet.

Prevention of -induced , , and fatty liver (steatosis) by tamoxifen was abrogated in mice with ERα-AF1 deficiency. According to Dr. Gourdy, "Altogether, these data indicate that activation of ERα-AF1 by tamoxifen is sufficient to elicit metabolic protective effects in vivo." In addition, the researchers found that selective activation of ERα-AF1 by tamoxifen also regulated most hepatic metabolic genes.

"Altogether, the present study first suggests that the of tamoxifen, as well as other selective modulators of ERα, deserve to be cautiously reconsidered in women, according to their menopausal status. It also opens new perspectives for the treatment of obesity-related complications toward a pharmacologic strategy eliciting selective ERα-AF1 activation," noted Dr. Gourdy.

More information: "Selective Activation of Estrogen Receptor α Activation Function-1 Is Sufficient to Prevent Obesity, Steatosis and Insulin Resistance in Mouse," American Journal of Pathology (2017). DOI: 10.1016/j.ajpath.2017.02.013

Journal information: American Journal of Pathology
Provided by Elsevier
Citation: Tamoxifen protects against obesity-related metabolic disorders (2017, May 11) retrieved 2 March 2024 from https://medicalxpress.com/news/2017-05-tamoxifen-obesity-related-metabolic-disorders.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

New gene discovered driving drug resistance


Feedback to editors