There is growing evidence that certain gut bacteria may contribute to high blood pressure (hypertension), along with smoking, high-sodium diets, and stress. In a few studies, when gut bacteria were killed off with antibiotics, patients with hypertension saw a drop in blood pressure.
And when gut bacteria were transplanted from hypertensive people into normal mice, they developed high blood pressure. The evidence is compelling, but until now, scientists have not identified a mechanism to explain how bacteria increase blood pressure.
Researchers from the University of Illinois and Brown University are pursuing a promising lead. Jason Ridlon, an assistant professor in the Department of Animal Sciences at U of I, first discovered the gene for an enzyme in certain bacteria that changes cortisol, a steroid hormone, into another steroid known as an androgen.
Gut Bacteria Metabolism
Ridlon worked with endocrinologist David Morris at Brown and found that when bacteria break that androgen down further, the end product, a molecule called a GALF, disrupts a process that regulates sodium transport out of human kidney cells. When that happens, sodium builds up in cells, and blood pressure rises.
To maintain normal blood pressure, a particular receptor has to bind with a molecule called aldosterone and then move into the cell nucleus. That sparks a cascade of reactions whose end-product is a protein that manages normal sodium and potassium transport into and out of the cell. But the receptor can be fooled, binding to cortisol instead of aldosterone.
If that happens, as it does in rare individuals with a disease called apparent mineralocorticoid excess (AME), the cascade of reactions goes into hyperdrive. Sodium is imported faster than it can be exported, and the cell begins to swell into a dangerous hypertensive state.
In normal individuals, an enzyme called 11βHSD2 acts as the guardian of that receptor, keeping cortisol from binding by changing it to cortisone.
GALFs – and there are a number of them – stop 11βHSD2 from working. Cortisol floods the receptor binding sites, and hypertension ensues as previously described.
From a different research effort, Ridlon has found that not all gut bacteria metabolize cortisol in the same way, or generate GALFs.
“There are probably multiple mechanisms through which gut bacteria can affect hypertension, but this is one that needs to be pursued,” Ridlon says. “Two people might have same amount of the bacterium Clostridium scindens, for example, but one person might have the type that has the pathway for generating these steroids. You can only tell by quantifying the genes, but we have to find them first.”
In a recent article he does just that, reporting the genes involved in GALF formation in Butyricicoccus desmolans.
“The next step is trying to see if these pathways correlate in patients that have certain forms of hypertension,” Ridlon says. “Are there higher abundances of these genes?”
The hope is that one day the research will lead to a drug therapy to combat hypertension. Ridlon says if they are better able to understand what the bacteria are doing, it would be possible to develop inhibitors of the enzymes that produce GALFs in these bacteria.
David J. Morris, Jason M. Ridlon
Glucocorticoids and gut bacteria: “The GALF Hypothesis” in the metagenomic era
Steroids, 2017; 125: 1 DOI: 10.1016/j.steroids.2017.06.002