Who has tried Isradipine?
With a new clinical trial it brings up the question of how many PD patients have already tried Isradipine?
|
Isradipine
Quote:
parkinsonsfocustoday.blogspot.com/ He has been on Isradipine since 2007 Good luck. If my forum does not allow me to post a URL -as I am a new member, Google search Parkinsonsfocustoday Kenki |
Isradipine
Quote:
Who is Steve? He writes well and sounds like a conservative scientist. Robert |
I have
I've been on Isradipine since 2007 as well.
|
Quote:
Robert |
fine
Robert, I'm doing fine - no problems with dynacirc cr. (I've been taking it since Dr. Surmeir spoke at PAN a couple of years ago - 2007?) it controls my hypertension. of course i have no evidence of what it does for pd. BUT i have had spect scans in 2003-05-07-09 (from a different clinical trial) and I hope at some point that they can be sent to dr. surmeir for anecdocal data if nothing else.
i think my pd progression is slow - haven't had to adjust my meds in quite a while - nearly 2 years maybe. current meds: azilect, stalevo 100 3x, mirapex .25 3x, requip xl 3 tablets 1x, dynacirc cr 5mg 2x, lexapro 1.0 jean |
Quote:
Robert |
exercise too
Robert,
I also exercise at least an hour a day - riding my trike, wii, swim ... Jean |
do I remember right....
That this is a calcium channel blocker? In reading about ginger for the other thread, I found reference to it also being one. Interesting.
|
here
Not sure where to put this so I will do both but suggest that we discuss in the other one-
1: J Cardiovasc Pharmacol. 2005 Jan;45(1):74-80. Ginger lowers blood pressure through blockade of voltage-dependent calcium channels. Ghayur MN, Gilani AH. Department of Biological and Biomedical Sciences, The Aga Khan University Medical College, Karachi, Pakistan. Ginger (Zingiber officinale Roscoe), a well-known spice plant, has been used traditionally in a wide variety of ailments including hypertension. We report here the cardiovascular effects of ginger under controlled experimental conditions. The crude extract of ginger (Zo.Cr) induced a dose-dependent (0.3-3 mg/kg) fall in the arterial blood pressure of anesthetized rats. In guinea pig paired atria, Zo.Cr exhibited a cardiodepressant activity on the rate and force of spontaneous contractions. In rabbit thoracic aorta preparation, Zo.Cr relaxed the phenylephrine-induced vascular contraction at a dose 10 times higher than that required against K (80 mM)-induced contraction. Ca2+ channel-blocking (CCB) activity was confirmed when Zo.Cr shifted the Ca2+ dose-response curves to the right similar to the effect of verapamil. It also inhibited the phenylephrine (1 microM) control peaks in normal-Ca2+ and Ca2+-free solution, indicating that it acts at both the membrane-bound and the intracellular Ca2+ channels. When tested in endothelium-intact rat aorta, it again relaxed the K-induced contraction at a dose 14 times less than that required for relaxing the PE-induced contraction. The vasodilator effect of Zo.Cr was endothelium-independent because it was not blocked by L-NAME (0.1 mM) or atropine (1 microM) and also was reproduced in the endothelium-denuded preparations at the same dose range. These data indicate that the blood pressure-lowering effect of ginger is mediated through blockade of voltage-dependent calcium channels. PMID: 15613983 [PubMed - indexed for MEDLINE] |
All times are GMT -5. The time now is 11:35 AM. |
Powered by vBulletin Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
vBulletin Optimisation provided by
vB Optimise v2.7.1 (Lite) -
vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.