Researchers present novel principle for nitric oxide-mediated signalling in blood vessels
Although a simple molecule, nitric oxide is an important signal substance that helps to reduce blood pressure by relaxing the blood vessels. But how it goes about doing this has long been unclear. Researchers at Karolinska Institutet in Sweden now present an entirely novel principle that challenges the Nobel Prize-winning hypothesis that the substance signals in its gaseous form. Their findings are presented in the journal Nature Chemical Biology.
That the simple molecule nitric oxide or nitrogen monoxide (NO) serves as a signal substance in many important physiological processes has been known for some time. For example, the discovery of the compound’s significance was awarded the 1998 Nobel Prize in Physiology or Medicine.
One of its functions is to initiate a signalling cascade that causes the smooth muscles of the vasculature to relax, thus expanding the vessels and lowering blood pressure. This is also why nitroglycerin, which releases NO, has long been a common treatment for angina.
However, the results now presented surprisingly indicate that it is not the NO molecule per se that is the active partner in the chemical interaction.
Possible paradigm shift
“It’s a little controversial, something of a paradigm shift in the field, in fact,” says Professor Jon Lundberg, who is the main author of the paper together with Andrei Kleschyov and Mattias Carlström, all of whom are at the Department of Physiology and Pharmacology, Karolinska Institutet.
The NO is formed in the endothelium, the tissue that constitutes the inner lining of blood vessels. For almost 40 years, the hypothesis has been that it then diffuses as a gas, spreading out randomly until it encounters an enzyme called guanylyl cyclase in the vascular smooth muscle, upon which the vessel relaxes. It is a journey over a distance of less than a millimetre, but it is a long way for a molecule.
“It’s hard to believe that it can work, since NO is so reactive and volatile that it ought to have trouble surviving that journey,” says Professor Lundberg.
Since it has also been difficult to demonstrate the presence of free NO in the cells, the actual signalling mechanism has long been a mystery.
A new signal substance
The KI group has tested the hypothesis that NO bonds with a “heme group”, a complex surrounding a single iron atom that is found in haemoglobin and that is freely available also in endothelial cells. Together they form a new and much more stable compound: NO-ferroheme. This hypothesis was formulated in 2017 by Andrei Kleschyov, who is the corresponding author of the new article.
The researchers found that NO-ferroheme significantly expands the blood vessels of mice and rats, and that in controlled experiments directly activates guanylyl cyclase, thus acting as a signal substance in the signal cascade.
“What we need to do now is establish that the endogenous NO-ferroheme that’s formed in endothelial cells really is a true signal substance and ascertain exactly how it gets synthesised in the body,” says Professor Lundberg.
Their results can provide a more detailed understanding of the chemical interaction and eventually open the way for new, improved treatments for cardiovascular disease.
The study was financed by the Swedish Research Council, the Swedish Heart-Lung Foundation, Novo Nordisk, the EFSD/Lilly European Diabetes Research Programme, the Ekhaga Foundation and Karolinska Institutet. Andrei Kleschyov is the inventor of a patent related to NO-heme. Jon Lundberg and Eddie Weitzberg are co-inventors for a patent application related to the therapeutic use of inorganic nitrate. No other conflicts of interest have been reported.
“NO-ferroheme is a signaling entity in the vasculature”, Andrei L. Kleschyov, Zhengbing Zhuge, Tomas A. Schiffer, Drielle D. Guimarães, Gensheng Zhang, Marcelo F. Montenegro, Angela Tesse, Eddie Weitzberg, Mattias Carlström, Jon O. Lundberg. Nature Chemical Biology, online 14 September 2023, doi: 10.1038/s41589-023-01411-5.