LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Why do cholinergic agents make brain for worse?

 - UBBFriend: Email this page to someone!    
Author Topic: Why do cholinergic agents make brain for worse?
lymeHerx001
Frequent Contributor (1K+ posts)
Member # 6215

Icon 1 posted      Profile for lymeHerx001     Send New Private Message       Edit/Delete Post   Reply With Quote 
I just picked up some Shisandra at the local health food store. I have read that it helps support the liver and we all know we need that.

I took one and now I feel my heart racing and my fog is kicking in.

I dont get it? When I looked up why it has stimulating properties it says that its cholinergic meaning that it increases acetylcholine release of mimics it.

When I take DMAE or choline or piracetam (all of which effect choline) my brain fog gets much worse.

This never used to happen.

Why is this?

Posts: 2905 | From New England | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
lymeHerx001
Frequent Contributor (1K+ posts)
Member # 6215

Icon 1 posted      Profile for lymeHerx001     Send New Private Message       Edit/Delete Post   Reply With Quote 
^
Posts: 2905 | From New England | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't totally understand this either. When hubby had really bad episodes of tremors I could give him IV phenergan (an anticholinergic) to stop the tremors.

But he could take lecithin or phosphatidylcholine without a problem.

My guess is that at times his brain was agitated by something and the anticholinergic slowed down the nerve impulses.

I do know that mercury can block the receptor sites (for dopamine I think) and I think that is why it can cause tremors. Choline is the gas and dopamine is the brakes for the nerves.

Lecithin and choline also detox the liver so that could be the cause of the brain fog. IV phosphatidylcholine (the P.K. protocol) lowered hubby's GGT to normal.

I would try very low doses of the shisandra or other cholinergic things and see if you adjust over time.

This is not medical advice, just my opinion based on hubby's experiences.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
lymeHerx001
Frequent Contributor (1K+ posts)
Member # 6215

Icon 1 posted      Profile for lymeHerx001     Send New Private Message       Edit/Delete Post   Reply With Quote 
thanks for trying. I need a team!

In fact why cant the just build an island for all of us and the doctors to figure it all out. What would be wrong with that.

Ill sign.

Posts: 2905 | From New England | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
dan67
LymeNet Contributor
Member # 20344

Icon 1 posted      Profile for dan67     Send New Private Message       Edit/Delete Post   Reply With Quote 
up. This is interesting. Anyone else have any input?
Posts: 641 | From Nevada | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
Wolfed Out
LymeNet Contributor
Member # 23727

Icon 1 posted      Profile for Wolfed Out     Send New Private Message       Edit/Delete Post   Reply With Quote 
dan,

It's real interesting for me for a number of reasons.

1. I developed Cholinergic Urticaria about 10 years, which is activated by exposure to heat, the sun, and exercise. At this time, I couldn't even take anti-histamines to resolve the issue, because they made my hives even worse. I found drinking alcohol reduced them.

2. I have several supplement problems, and unusual medication reactions. I'm trying to implicate this area as the cause.

3.....

I just had an OMG moment.

I was taking a supplement called RegeneMAX which contains Choline in the form Choline-Stabilized Orthosilicic Acid. I couldn't tolerate the supplement, even though it's supposed to be support for hair and skin.

I was having severe difficulty thinking while taking it, and my skin was looking unhealthier.

Dont know what this means yet... Hopefully someone will CHIME IN!

Posts: 829 | From MD | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
dan67
LymeNet Contributor
Member # 20344

Icon 1 posted      Profile for dan67     Send New Private Message       Edit/Delete Post   Reply With Quote 
I react very poorly to taking lecithin which is primarily choline. I wanted to take it to help bile formation.

But what is very bizarre, is the fact that egg yolk (which contains a ton of choline) makes me feel GREAT. For some reason, my body likes the natural choline but not the pill form. And I'm not allergic to soy, which is the kind of lecithin I have in supplement form. They make lecithin from sunflower in supplement form, but at this point I think I'll ditch the choline supplements and stick with consuming egg yolks regularly.

Posts: 641 | From Nevada | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.