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Re: Investor2014 post# 175991

Monday, 12/24/2018 11:55:16 AM

Monday, December 24, 2018 11:55:16 AM

Post# of 517499
High occupancy of s1 receptors in the human brain after single oral administration of donepezil: a positron emission tomography study using [11C]SA4503



“The acetylcholinesterase (AChE) inhibitor donepezil is also a s1 receptor agonist. We examined whether donepezil binds to s1 receptors in the living human brain after a single oral administration. Dynamic positron emission tomography (PET) data acquisition using the selective s1 receptor ligand [11C]SA4503 was performed to evaluate quantitatively the binding of [11C]SA4503 to s1 receptors in eight healthy male volunteers. Each subject had a PET scan before and after receiving a single dose of donepezil (5 or 10 mg). The binding potential of [11C]SA4503 was calculated. Doses of 5 mg and 10 mg donepezil bound to s1 receptors in the human brain with occupancies of ~60% and ~75%, respectively, in a dose-dependent manner. This study demonstrated that donepezil binds to s1 receptors in the living human brain at therapeutic doses. Therefore, s1 receptors may be implicated in the pharmacological mechanism of donepezil in the human brain. “

https://academic.oup.com/ijnp/article/12/8/1127/678305

A bit puzzling to me how donepezil does not apparently have an impact on A2-73 results disclosed thus far by Anavex. Wasn’t (2-73 plus) 5mgs of donepezil plus 2-73?

As I understand it Sigma1 one agonists competes with any other in a winner take all fashion. Can both bind concurrently at different receptor locations?


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