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'Love hormone' from insects as potential drug lead for inhibiting preterm labor

Date:
February 1, 2017
Source:
Medical University of Vienna
Summary:
An oxytocin-like neuropeptide ("inotocin") exhibited a specific pharmacological profile for the human receptors of oxytocin (known as the "love hormone") and vasopressin, report scientists at conclusion of their study. At the same time, the researchers were able to show that a synthetic analogue of inotocin serves as a molecular tool for the fundamental understanding of biochemical signalling processes of oxytocin and vasopressin receptors and could possibly be used as drug lead molecule to develop pharmaceuticals for inhibiting preterm labor, for example.
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In a recent study published in Scientific Reports, an international team of researchers led by MedUni Vienna report that an oxytocin-like neuropeptide ("inotocin") exhibited a specific pharmacological profile for the human receptors of oxytocin (known as the "love hormone") and vasopressin. At the same time, the researchers were able to show that a synthetic analogue of inotocin serves as a molecular tool for the fundamental understanding of biochemical signalling processes of oxytocin and vasopressin receptors and could possibly be used as drug lead molecule to develop pharmaceuticals for inhibiting preterm labor, for example.

A team of scientists from Austria, Australia, Denmark, England and the Czech Republic, led by Christian Gruber from the MedUni Vienna's Institute of Pharmacology managed to isolate a neuropeptide from ants that is very similar to the human "love hormone" oxytocin, and the closely related hormone vasopressin. "Surprisingly, by introducing a small chemical modification into this insect neuropeptide, we were able to develop a very stable and highly selective inhibitor of the human vasopressin V1a receptor," explains Christian Gruber. "This ligand was tested on human uterine tissue and effectively inhibited muscular contractions. Further tests are now necessary to explore clinical applications of the active lead molecule."

Preventing uterine contractility in preterm labor

Vasopressin (also known as the anti-diuretic hormone) plays an important role in regulating water balance through the kidneys; however, in combination with oxytocin, it can also influence the blood supply to the uterus and uterine contractility during childbirth. An inhibitor for the human vasopressin V1a receptor could therefore be given to patients at risk of premature labor to inhibit undesirable, preterm uterine muscle contractions. The vasopressin V1a receptor also plays an important role in the brain and in the cardiovascular system. Hence, there are other conceivable clinical applications -- for example, to treat anxiety disorders, aggression, depression, as well as congestive heart failure, stroke or menstrual pain.

The recently published study is part of a life science project (LS13-017) funded by the Vienna Science and Technology Fund (WWTF).

600-million-year-old oxytocin-vasopressin signalling system

In order to decode or uncover such relationships between neuropeptide hormones and their receptors, the researchers used a unique strategy for ligand discovery, exploiting the advantages of the evolutionary similarities of the oxytocin-vasopressin signalling system, which exists since about 600 million years. Comparing these related receptors at a molecular level provides new insights and allows the identification of important receptor residues that might aid the development of better drug candidates in the future. "Our concept is innovative and fascinating: take an insect neuropeptid, skip over approximately 600 million years of evolution and, with a small chemical modification, this substance may be suitable to act as a drug candidate for use in humans," explains Gruber. "It is equally important to utilize these new molecules as research "tools." Only by developing receptor subtype-selective ligands, it will be possible to investigate the biochemical principles of such complex signalling systems," adds Gruber.

Oxytocin-vasopressin signalling system throughout the animal kingdom?

Unlike for other animals, there has so far been little information available about the biology of this neuropeptide signalling system in insects. "In a parallel study, by analysing genetic data sets, we have now been able to show that many insects have an oxytocin or vasopressin-like signalling system, and it is presumably functionally related throughout the animal kingdom," reports Gruber. With this information in hand, the future aim of the researchers is to explain the physiology and pharmacology of this signalling system in insects, and utilize this information to develop novel pharmaceutical tools or drug candidates for humans.


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Materials provided by Medical University of Vienna. Note: Content may be edited for style and length.


Journal References:

  1. Zita Liutkeviciute, Johannes Koehbach, Thomas Eder, Esther Gil-Mansilla, Christian W. Gruber. Global map of oxytocin/vasopressin-like neuropeptide signalling in insects. Scientific Reports, 2016; 6: 39177 DOI: 10.1038/srep39177
  2. Maria Giulia Di Giglio, Markus Muttenthaler, Kasper Harpsøe, Zita Liutkeviciute, Peter Keov, Thomas Eder, Thomas Rattei, Sarah Arrowsmith, Susan Wray, Ales Marek, Tomas Elbert, Paul F. Alewood, David E. Gloriam, Christian W. Gruber. Development of a human vasopressin V1a-receptor antagonist from an evolutionary-related insect neuropeptide. Scientific Reports, 2017; 7: 41002 DOI: 10.1038/srep41002

Cite This Page:

Medical University of Vienna. "'Love hormone' from insects as potential drug lead for inhibiting preterm labor." ScienceDaily. ScienceDaily, 1 February 2017. <www.sciencedaily.com/releases/2017/02/170201093449.htm>.
Medical University of Vienna. (2017, February 1). 'Love hormone' from insects as potential drug lead for inhibiting preterm labor. ScienceDaily. Retrieved May 24, 2017 from www.sciencedaily.com/releases/2017/02/170201093449.htm
Medical University of Vienna. "'Love hormone' from insects as potential drug lead for inhibiting preterm labor." ScienceDaily. www.sciencedaily.com/releases/2017/02/170201093449.htm (accessed May 24, 2017).

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