Scientists at Indiana University and international collaborators have found a way to link two hormones into a single molecule, producing a more effective therapy with fewer side effects for potential use as treatment for obesity and related medical conditions.
The studies were carried
out in the laboratories of Richard DiMarchi, the Standiford H. Cox
Distinguished Professor of Chemistry and the Linda & Jack Gill Chair in
Biomolecular Sciences in the IU Bloomington College of Arts and Sciences, and
of Matthias Tschöp, professor of medicine and director of the Institute of
Diabetes and Obesity, Helmholtz Center Munich, Germany.
Results were published
online this week by the journal Nature
Medicine.
Researchers combined a
peptide hormone from the digestive system, GLP-1, with the hormone estrogen and
administered it to obese laboratory mice. While both GLP-1 and estrogen have
demonstrated efficacy as therapy for obesity and adult-onset diabetes, the combination
was more effective in producing weight loss and other beneficial results than
using either compound on its own. And it produced fewer adverse effects, such
as excessive tissue growth linked to tumor formation.
"We find that
combining the hormones as a single molecule dramatically enhanced their
efficacy and their safety," DiMarchi said. "The combination improves
the ability to lower body weight and the ability to manage glucose, and it does
so without showing the hallmark toxicities associated with estrogen."
The researchers believe
GLP-1 acts as a "medicinal chaperone," targeting estrogen to the
hypothalamus and pancreas, which are involved with metabolic processes. The
precise targeting reduces the likelihood that the estrogen will produce negative
effects, such as cancer and stroke.
Brian Finan, a former
doctoral student in DiMarchi's lab, is the lead author of the paper,
"Targeted estrogen delivery reverses the metabolic syndrome."
Co-authors include Bin Yang and Vasily Gelfanov, research scientists in the IU
Bloomington Department of Chemistry, and DiMarchi. Finan is now a post-doctoral
researcher at the Helmholtz Zentrum München in Germany, directed by Tschöp, who
is DiMarchi's longtime collaborator and a corresponding co-author. Affiliations
of the other 20 co-authors include the University of Cincinnati where, also led
by Tschöp, many of the in vivo pharmacology and molecular mechanism studies
were conducted; Northwestern University; and research laboratories in Germany
and China.
Associated with what health
authorities are calling a global epidemic of obesity, the metabolic syndrome
consists of obesity associated with other factors such as high blood pressure,
high triglycerides, hyperglycemia and low HDL cholesterol. The International
Diabetes Federation estimates that as much as 20 percent of the world's adult
population has some form of the metabolic syndrome and that they are three
times as likely to have a heart attack or stroke and five times as likely to
develop adult-onset diabetes as people without the syndrome.
DiMarchi said investigation
continues in the optimization of the peptide-based hormone conjugates with an
emphasis on determining the specific mechanism of biological action and
identification of an optimal drug candidate suitable for human study. The
combination of other peptides and nuclear hormones for targeting other medical
conditions holds considerable promise and opportunity for future research.
Partial funding of the
research was provided by Marcadia Biotech and more recently Roche Pharma.
Marcadia is a company that DiMarchi co-founded and was acquired in 2010 by
Roche Pharma, to which he remains a research consultant.
Journal Reference:
1. Brian
Finan, Bin Yang, Nickki Ottaway, Kerstin Stemmer, Timo D Müller, Chun-Xia Yi,
Kirk Habegger, Sonja C Schriever, Cristina García-Cáceres, Dhiraj G Kabra,
Jazzminn Hembree, Jenna Holland, Christine Raver, Randy J Seeley, Wolfgang
Hans, Martin Irmler, Johannes Beckers, Martin Hrabě de Angelis, Joseph P Tiano,
Franck Mauvais-Jarvis, Diego Perez-Tilve, Paul Pfluger, Lianshan Zhang, Vasily
Gelfanov, Richard D DiMarchi, Matthias H Tschöp.Targeted estrogen
delivery reverses the metabolic syndrome. Nature Medicine, 2012; DOI: 10.1038/nm.3009
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