Drinking baking soda could be an
inexpensive, safe way to combat autoimmune disease
Medical College of Georgia at
Augusta University
A daily dose of baking soda may help
reduce the destructive inflammation of autoimmune diseases like rheumatoid
arthritis, scientists say.
They have some of the first evidence
of how the cheap, over-the-counter antacid can encourage our spleen to promote
instead an anti-inflammatory environment that could be therapeutic in the face
of inflammatory disease, Medical College of Georgia scientists report in
the Journal of Immunology.
They have shown that when rats or
healthy people drink a solution of baking soda, or sodium bicarbonate, it
becomes a trigger for the stomach to make more acid to digest the next meal and
for little-studied mesothelial cells sitting on the spleen to tell the
fist-sized organ that there's no need to mount a protective immune response.
"It's most likely a hamburger
not a bacterial infection," is basically the message, says Dr. Paul
O'Connor, renal physiologist in the MCG Department of Physiology at Augusta
University and the study's corresponding author.
Mesothelial cells line body cavities, like the one that contains our digestive tract, and they also cover the exterior of our organs to quite literally keep them from rubbing together. About a decade ago, it was found that these cells also provide another level of protection.
They have little fingers, called microvilli, that sense the environment, and warn the organs they cover that there is an invader and an immune response is needed.
Drinking baking soda, the MCG
scientists think, tells the spleen -- which is part of the immune system, acts
like a big blood filter and is where some white blood cells, like macrophages,
are stored -- to go easy on the immune response. "Certainly drinking
bicarbonate affects the spleen and we think it's through the mesothelial
cells," O'Connor says.
The conversation, which occurs with
the help of the chemical messenger acetylcholine, appears to promote a
landscape that shifts against inflammation, they report.
In the spleen, as well as the blood
and kidneys, they found after drinking water with baking soda for two weeks,
the population of immune cells called macrophages, shifted from primarily those
that promote inflammation, called M1, to those that reduce it, called M2.
Macrophages, perhaps best known for their ability to consume garbage in the body like debris from injured or dead cells, are early arrivers to a call for an immune response.
Macrophages, perhaps best known for their ability to consume garbage in the body like debris from injured or dead cells, are early arrivers to a call for an immune response.
In the case of the lab animals, the
problems were hypertension and chronic kidney disease, problems which got
O'Connor's lab thinking about baking soda.
One of the many functions of the
kidneys is balancing important compounds like acid, potassium and sodium. With
kidney disease, there is impaired kidney function and one of the resulting
problems can be that the blood becomes too acidic, O'Connor says. Significant
consequences can include increased risk of cardiovascular disease and
osteoporosis.
"It sets the whole system up to
fail basically," O'Connor says. Clinical trials have shown that a daily
dose of baking soda can not only reduce acidity but actually slow progression
of the kidney disease, and it's now a therapy offered to patients.
"We started thinking, how does
baking soda slow progression of kidney disease?" O'Connor says.
That's when the anti-inflammatory
impact began to unfold as they saw reduced numbers of M1s and increased M2s in
their kidney disease model after consuming the common compound.
When they looked at a rat model
without actual kidney damage, they saw the same response. So the basic
scientists worked with the investigators at MCG's Georgia Prevention Institute
to bring in healthy medical students who drank baking soda in a bottle of water
and also had a similar response.
"The shift from inflammatory to an anti-inflammatory profile is happening everywhere," O'Connor says. "We saw it in the kidneys, we saw it in the spleen, now we see it in the peripheral blood."
The shifting landscape, he says, is likely due to increased conversion of some of the proinflammatory cells to anti-inflammatory ones coupled with actual production of more anti-inflammatory macrophages.
The scientists also saw a shift in other immune cell types, like more regulatory T cells, which generally drive down the immune response and help keep the immune system from attacking our own tissues. That anti-inflammatory shift was sustained for at least four hours in humans and three days in rats.
The shift ties back to the
mesothelial cells and their conversations with our spleen with the help of
acetylcholine. Part of the new information about mesothelial cells is that they
are neuron-like, but not neurons O'Connor is quick to clarify.
"We think the cholinergic
(acetylcholine) signals that we know mediate this anti-inflammatory response
aren't coming directly from the vagal nerve innervating the spleen, but from
the mesothelial cells that form these connections to the spleen," O'Connor
says.
In fact, when they cut the vagal
nerve, a big cranial nerve that starts in the brain and reaches into the heart,
lungs and gut to help control things like a constant heart rate and food
digestion, it did not impact the mesothelial cells' neuron-like behavior.
The affect, it appears, was more
local because just touching the spleen did have an effect.
When they removed or even just moved
the spleen, it broke the fragile mesothelial connections and the
anti-inflammatory response was lost, O'Connor says. In fact, when they only
slightly moved the spleen as might occur in surgery, the previously smooth
covering of mesothelial cells became lumpier and changed colors.
"We think this helps explain
the cholinergic (acetylcholine) anti-inflammatory response that people have
been studying for a long time," O'Connor says.
Studies are currently underway at
other institutions that, much like vagal nerve stimulation for seizures,
electrically stimulate the vagal nerve to tamp down the immune response in
people with rheumatoid arthritis.
While there is no known direct connection between the vagal nerve and the spleen -- and O'Connor and his team looked again for one -- the treatment also attenuates inflammation and disease severity in rheumatoid arthritis, researchers at the Feinstein Institute for Medical Research reported in 2016 in the journal Proceedings of the National Academy of Sciences.
While there is no known direct connection between the vagal nerve and the spleen -- and O'Connor and his team looked again for one -- the treatment also attenuates inflammation and disease severity in rheumatoid arthritis, researchers at the Feinstein Institute for Medical Research reported in 2016 in the journal Proceedings of the National Academy of Sciences.
O'Connor hopes drinking baking soda
can one day produce similar results for people with autoimmune disease.
"You are not really turning
anything off or on, you are just pushing it toward one side by giving an
anti-inflammatory stimulus," he says, in this case, away from harmful
inflammation. "It's potentially a really safe way to treat inflammatory
disease."
The spleen also got bigger with
consuming baking soda, the scientists think because of the anti-inflammatory
stimulus it produces. Infection also can increase spleen size and physicians
often palpate the spleen when concerned about a big infection.
Other cells besides neurons are
known to use the chemical communicator acetylcholine. Baking soda also interact
with acidic ingredients like buttermilk and cocoa in cakes and other baked
goods to help the batter expand and, along with heat from the oven, to rise. It
can also help raise the pH in pools, is found in antacids and can help clean
your teeth and tub.
The research was funded by the
National Institutes of Health.