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Venthamarai chooranam, a polyherbal Siddha medicine, alleviates hypertension via AT 1 R and eNOS signaling pathway in 2K1C hypertensive rats
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The present study was aimed to scientifically demonstrate the anti-hypertensive action of Venthamarai chooranam (VMC) in renal hypertensive rats. Two Kidney One Clip (2K1C) Goldblatt model was adopted to induce hypertension in rats. Male Sprague Dawley rats (270–320 g) were randomized into sham ( n = 6), vehicle-treated 2K1C ( n = 9) and VMC-treated 2K1C (400 mg/kg, p.o; n = 8) and monitored for nine weeks. Systolic blood pressure (SBP), plasma nitrate/nitrite, carotid endothelial nitric oxide synthetase (eNOS), renal angiotensin type 1 receptor (AT
1
R), angiotensin type 2 receptor (AT
2
R), TNFα, IL-6, thioredoxin 1 (TRX1), and thioredoxin reductase 1 (TRXR1) mRNA expressions were studied. VMC upregulated eNOS expression which in turn improved plasma nitric oxide and decreased SBP in hypertensive rats. It down-regulated AT
1
R and simultaneously upregulated AT
2
R expression in comparison to vehicle-treated 2K1C rats. Further, renal TNFα and IL-6 expressions were down-regulated while TRX1 and TRXR1 were upregulated by VMC. VMC potentially interacts with renin-angiotensin components and endothelial functions, and thereby exerts its antihypertensive action. This is the first study to demonstrate the mechanism of anti-hypertensive action of VMC in an animal model of renovascular hypertension.
Title: Venthamarai chooranam, a polyherbal Siddha medicine, alleviates hypertension via AT
1
R and
eNOS
signaling pathway in 2K1C hypertensive rats
Description:
The present study was aimed to scientifically demonstrate the anti-hypertensive action of Venthamarai chooranam (VMC) in renal hypertensive rats.
Two Kidney One Clip (2K1C) Goldblatt model was adopted to induce hypertension in rats.
Male Sprague Dawley rats (270–320 g) were randomized into sham ( n = 6), vehicle-treated 2K1C ( n = 9) and VMC-treated 2K1C (400 mg/kg, p.
o; n = 8) and monitored for nine weeks.
Systolic blood pressure (SBP), plasma nitrate/nitrite, carotid endothelial nitric oxide synthetase (eNOS), renal angiotensin type 1 receptor (AT
1
R), angiotensin type 2 receptor (AT
2
R), TNFα, IL-6, thioredoxin 1 (TRX1), and thioredoxin reductase 1 (TRXR1) mRNA expressions were studied.
VMC upregulated eNOS expression which in turn improved plasma nitric oxide and decreased SBP in hypertensive rats.
It down-regulated AT
1
R and simultaneously upregulated AT
2
R expression in comparison to vehicle-treated 2K1C rats.
Further, renal TNFα and IL-6 expressions were down-regulated while TRX1 and TRXR1 were upregulated by VMC.
VMC potentially interacts with renin-angiotensin components and endothelial functions, and thereby exerts its antihypertensive action.
This is the first study to demonstrate the mechanism of anti-hypertensive action of VMC in an animal model of renovascular hypertension.
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