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Pyridostigmine (brand: Mestinon) is an acetylcholinesterase inhibitor. Pyridostigmine is poorly absorbed in the gut and does not cross the blood-brain barrier.

Pyridostigmine works by preventing the breakdown of acetylcholine (ACh) in nervous system synapses. This leads to an increase in acetylcholine, a neurotransmitter widely found in both the peripheral and central nervous systems. Acting as both an excitatory and inhibitory neurotransmitter, acetylcholine performs a variety of functions. Within the skeletal muscular system it contracts muscle, allowing for movement. It slows the heart, and promotes REM sleep. In the central nervous system, ACh is closely associated with learning, attention, and short-term memory.

Pyridostigmine is mainly prescribed for myasthenia gravis, an autoimmune condition in which acetylcholine is blocked, leading to profound muscle weakness. In spite of the fact that it does not cross the blood-brain barrier, pyridostigmine is also used to enhance memory in people with Alzheimer's disease. Pyridostigmine has been administered as a treatment for the paralysis caused by organophosphate pesticide poisoning. In a similar vein, the military administered pyridostigmine as a prophylactic to soldiers during the Gulf War to block potential exposure to Soman, a nerve gas which acts on acetylcholine in much the same manner as organophosphate pesticides. Recently, pyridostigmine has been used to treat orthostatic intolerance.

USES IN ME/CFS: In his book, Betrayal by the Brain, Dr. Jay Goldstein proposed that pyridostigmine could be used in ME/CFS with much the same results as in patients with myasthenia gravis, namely the alleviation of muscle weakness. Surprisingly, Dr. Goldstein found that even though pyridostigmine does not cross the blood-brain barrier it increased mental clarity in his ME/CFS patients. He noted that because pyridostigmine helps increase the secretion of growth hormone (GH), it might be of benefit to ME/CFS patients, who tend to have low levels of GH.

In 2003 a group of Japanese researchers published a study in which low-dose pyridostigmine was administered to three ME/CFS patients with dysautonomia and positive Epstein-Barr virus (EBV) titers. In all three cases, a one-month course of pyridostigmine relieved fatigue and muscle weakness. The authors speculated that EBV infection induces antibodies, which, through an inhibition of calcium influx at motor terminals, reduces acetylcholine release and causes muscle weakness and cholinergic autonomic dysfunction. The authors concluded that their case studies “strongly suggest therapy using a small dose (10 mg per day) of oral pyridostigmine in patients with CFS who have had more than a 40% amplitude increase in response to the RNS [repetitive nerve stimulation] test, positive anti-VCA IgG of EBV and mild impairment of autonomic functions.”

Based on findings that pyridostigmine increases growth hormone, a 2008 study of fibromyalgia patients in Portland, Oregon was conducted comparing exercise, diet and treatment with pyridostigmine. While the researchers did not find that either pyridostigmine alone or pyridostigmine plus exercise produced an improvement in most FM symptoms, they did find that pyridostigmine improved anxiety and sleep. The authors speculated that pyridostigmine may have improved vagal tone, thus alleviating sleep and anxiety symptoms.


Treatment rating for Mestinon (pyridostigmine)

Rating keys:

1=LOW (I would not recommend this treatment)

5=HIGH (This treatment helped me a great deal)

Rating Side Effects Reason for Treatment Dosage / Duration Age Sex M/F # of years Ill Additional Comments Illness Severity Date Added
4 Almost immediately relieved symptoms of Orthostatic intolerance. Meant that I could sit and walk around without struggle, dizziness and nausea. Meant I had a little more energy for reading/writing/walking. Read about it from other PwME online. 6 month 60mg 2X day 27 Female 3 This is the only medication that has made some difference in my 3 years of ME. Moderate/Severe 06/20/18
4 Only good ones. Prescribed for POTS 30 day 30 mg 3X day 65 Female 15 Greater mental clarity, relieved dry eyes, relieved constipation. Moderate/Severe 08/12/18
4 Stomach upset Autonomic symptoms 1 year 180mg 1X day 49 Female 33 I was unable to sit up without feeling faint and had constant air hunger. This is the first medication that made me feel stronger. Moderate 07/18/19
5 Diarrhea at times if change times taken or add new doses for the first time. Double seronegative General Myasthenia Gravis, just diagnosed. 3 month 60 mg 6X day 58 Female 46 Mild 01/17/21
4 None For POTS and me/cfs 2 week 30 mg 3X day 47 Female 4 Helped immediately with my SIBO, my POTS was less pronounced and my muscles had more power,. Mestinon didn't improve pain or cognition. Tried Huperzine A which works similarly but crosses the blood brain barrier which helped with cognition. Unsure if I should take both as too much acetylcholine circulating can have side effects. Moderate/Severe 05/15/21
4 None so far neurogenic orthostatic hypotension 2 week 30 mg 3X day 59 Male 14 went from a dozen mild to moderate episodes a day to get a few after starting the drug - my fatigue has also improved greatly. Moderate/Mild 07/04/21
4 None so far neurogenic orthostatic hypotension 3 week 30 mg 3X day 59 Male 7 went from a dozen episodes of being lightheaded and presyncope a day to just a couple a week. My fatigue and weakness has also improved greatly. Moderate 07/15/21
5 none ME/CFS, POTS. Autonomic gut issues, lack of motility 1 month 30mg 2X day 39 Female 2 I no longer have constant GI pain and discomfort. Motility is improved. Moderate 03/02/22
5 - Muscle cramping - sometime severe. Settled down a little but still an issue. - Large flare-up of GERD - still is on-going. Need to take meds to keep it under control - Intestinal - had to cut back on my daily Magnesium - Lower blood pressue My ME/CFS has become worse over the past few years. Just a lack of energy. Plus no strength. 6 month 30 mg 2X day 63 Female 25 At first, this was an absolute miracle drug. Within just a few days the improvement was noticeable. More strength. Fatigue greatly reduce. However, the side effect management has been tricky and I also feel that my body has become accustomed to it and it's not working as well as it did. Part of that may be because I had to cut my dosage down from 180 mgs/day to 90 mgs/day. All that being said, I will continue to stay on it - the REM sleep improvement is HUGE. Moderate/Mild 06/02/22