Washington, May 12 (ANI): Anti-inflammatory drugs can help block the rapid kidney destruction that can occur with hypertension, claim Medical College of Georgia researchers.
They found that treating hypertensive rats with the broad-acting anti-inflammatory drug pentosan polysulfate preserves the kidney”s ability to regulate pressure placed on tiny filters called glomeruli.
A million of these fragile structures are responsible for filtering the body”s total plasma volume 60 times daily.
Therapeutic intervention is a long-term goal, said Dr. Edward W. Inscho, corresponding author.
“Because the job is big, the kidneys are vulnerable to injury. If we can keep them functioning longer, quality of life is going to be better longer,” he added.
However, he noted that this exact approach isn”t a treatment option primarily because of side effects that can result from long-term use of anti-inflammatory drugs.
Hypertension and diabetes take a similar toll on kidneys and together, the pervasive conditions are creating a rapidly growing number of patients in kidney failure.
“The number of people going to dialysis because of these two maladies just grows exponentially so there is a really good reason to figure this out,” said Inscho.
In a rather vicious circle, kidneys are hurt by and contribute to hypertension— which comes first remains unresolved.
But one key way hypertension hurts kidneys is by blunting the function of afferent arterioles, tiny blood vessels that feed the filtering units.
Much like a dam operator controls water flow into a river, a mechanosensor, likely located inside the smooth muscle cells that form the blood vessel walls, keeps tabs on the pressure of the blood flowing through the afferent arteriolar into the filters.
If pressure gets too high, it prompts the small vessel to contract.
“You want the vasculature to constrict because filters are very delicate and the kidneys want to keep blood flow and filtration relatively constant,” said Inscho.
He noted that this balancing act enables kidney tubules, which reabsorb good things like glucose and amino acids, to do their job.
His animal studies have shown that mechanosensor function falters after just three days of high blood pressure.
He also wants to study the role the inflammatory factors TGF-ß and MCP-1 play in arteriole dysregulation.
Both factors are elevated in high blood pressure and implicated in other types of vascular injury.
Preliminary evidence suggests that the factors set up some sort of signaling event that turns mechanosensors off or at least down.
Ironically, impaired autoregulation leads to increased production of the inflammatory factors.
“We have data that argue that TGF-ß can definitely cause these blood vessels to fail. If you apply the cytokine to a healthy kidney, the blood vessel will not respond correctly; wash it off and it does. Now we also have data that if we protect the kidneys from MCP-1, we can improve the function of these vessels,” said Inscho.
He”s looking at the impact of anti-inflammatory drugs pentosan polysulfate as well as mycophenolate mofetil because of existing evidence that their use reduces protein excretion in the urine, a sign of kidney damage.
Rather than as a potential therapy, he views the drugs as tools for helping dissect a complex process.
“Hypertension-related kidney damage is multifaceted, but part of that cascade of progression to injury is functional impairment of that blood vessel. We have established that, I think, unequivocally,” said Inscho.
“The grant will enable us to get more information about normal function and pathology all at the same time,” he added.
The study has been reported in the May issue of American Journal of Physiology – Renal Physiology. (ANI)