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    • Lowering BP : Salt...

    Lowering BP : Salt restriction more beneficial in women finds Hypertension study

    Written by Medha Baranwal Baranwal Published On 2018-12-17T20:28:48+05:30  |  Updated On 23 Aug 2021 4:32 PM IST

    Augusta, Georgia: Low salt diet s a hallmark for treatment of hypertension or high BP. Salt restriction is more beneficial in women than men for lowering BP, according to a new study. Also, drugs that directly block aldosterone benefits females. Aldosterone is a blood vessel constrictor and hormone that is naturally higher in female and further increased by a high-salt diet.

    The study, published in the journal Hypertension, found that while females have lower salt retention, but still there is an effect that increases the pressure.


    Salt-sensitive hypertension is more prevalent in women than men, indicate clinical studies. However, animal models of salt sensitivity have primarily focused on the mechanisms of salt sensitivity in male animals, therefore, there is a need for the elucidation of these mechanisms in female animal models.



    Eric Belin de Chantemele, physiologist in the Vascular Biology Center at the Medical College of Georgia at Augusta University, and colleagues hypothesized that female mice develop salt-sensitive increases in blood pressure to elucidate animal models of salt sensitivity on the mechanisms of salt sensitivity in female animals.


    Also Read: Too much salt in diet can cause irregular heartbeat

    After just seven days on a high-salt diet, the ability of female mice to relax blood vessels decreased while their blood pressure increased, says Dr. Belin de Chantemele.


    Treatment with the aldosterone antagonist eplerenone restored a healthier blood pressure and the ability of the lining of the blood vessels to relax, says Belin de Chantemele.


    Blood pressures in males and females were similar at the start of the studies and aldosterone levels were higher in the females, a typical difference between the sexes, which Belin de Chantemele had previously found.


    "We thought that if the female mice have more aldosterone than the males, they should be more salt- sensitive," says Belin de Chantemele. "That is what really pushed us to do this study."


    Eating too much salt is a daily occurrence for most of us and one of the aldosterone's functions is increasing sodium and fluid retention by the kidneys, the scientists say. There is supposed to be sort of seesaw effect so that when we eat too much salt, aldosterone levels go down so we don't retain too much salt, which drives up fluid retention and blood pressure.


    Also Read: Reducing salt intake to very low levels increases mortality risk

    The MCG scientists found that in males, the aldosterone-salt interaction action works: increased salt intake suppresses aldosterone, which helps protect males from this path to hypertension.


    However, females taking in a lot of salt don't suppress aldosterone as much, so aldosterone levels and blood pressure both are higher, Faulkner says.


    In this scenario, rather than holding onto more fluid and salt, aldosterone appears to cause problems by impairing the ability of blood vessels to relax. In fact, the scientists found no evidence that the kidneys, which should eliminate excessive sodium, were the problem. Both sexes excreted more sodium when they consumed more, and the females actually excreted the most.


    "In the salt-sensitivity field there are two main concepts," says Belin de Chantemele. "One is it's mediated by the kidney retaining more salt. Another one suggests that it's an improper relaxation of the blood vessels in people who are salt-sensitive. Our data support that second concept."


    When they used the drug, eplerenone - a diuretic that blocks the receptor for aldosterone and is already used to treat high blood pressure and more commonly heart failure - it restored blood pressure and endothelial function in the females.


    It decreased both day- and nighttime measures of the systolic blood pressure (top number which indicates pressure when the heart is contracting), diastolic pressure (bottom number, which indicates pressure when the heart is relaxed) and mean arterial pressure (an average between the two which gives an overall idea of blood flow).


    In males, the drug didn't affect any of those pressures or alter the function of the endothelial cells that line blood vessels and aid their contraction and relaxation.


    The findings provide more evidence that the aldosterone system is a particularly good target for females in the face of pathological problems like obesity and salt-sensitive hypertension, they write.


    The females actually experienced lower activity than males of the renin-angiotensin system, a kidney-based system for regulating blood pressure and fluid levels often targeted by common hypertension medications like ACE inhibitors.


    Clinical studies have indicated that females are generally more salt-sensitive, but those findings have not held up in animal studies - which mostly have been done in male rodents - until now.


    The INTERSALT study, for example, of more than 10,000 males and females worldwide from 1984-97 surmised that high salt intake is an important and preventable factor in increasing blood pressure trends and that females are more at risk than males for salt-sensitive increases in their blood pressure.

    blood pressureBPeplerenoneEric Belin de Chantemelefluid retentionHypertensionINTERSALT studylesslow saltlowering BPrenin angiotensin systemSaltsalt restrictionsalt retentionsalt sensitivesalt sensitivity
    Source : With inputs from Hypertension

    Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd

    Medha Baranwal Baranwal
    Medha Baranwal Baranwal
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