Biochemistry
Greenlighter
- Joined
- Jan 4, 2012
- Messages
- 18
I was a long term user of escitalopram (Cipralex UK/Lexapro US) for major depression. After four years of daily usage, this medication simply stopped working entirely. I am now taking citalopram and it is working much better than the escitalopram ever did, particularly in the area of anxiolysis. Although escitalopram is pretty good for depression, I found it to be hugely anxiogenic, and I also found that tolerance builds very quickly. However, I find citalopram to be equally as good for depression and equal to diazepam for generalised anxiety.
I believe that Lundbeck/Forest Laboratories, due to a desire to extend the patent life of its product, have utterly manipulated the academic literature and clinical trials data in relation to the S and R enantiomers of citalopram. Although I have no evidence to back up my theory (because it seems like all of the academic research has been sponsored by Lundbeck/Forest Laboratories), from personal experience and intuition, I believe that R-citalopram is largely responsible for the anxiolytic properties of citalopram. If you read the academic literature about S-citalopram and R-citalopram, they all mention that R-citalopram counteracts the "antidepressant and anxiolytic" properties of S-citalopram based 5HT release in the frontal cortex. This is entirely disingenuous because it does not mention other potential modes of action that R-citalopram has on other neurotransmitter systems, such as gamma-Aminobutyric acid (GABA), for example.
What are your thoughts?
I believe that Lundbeck/Forest Laboratories, due to a desire to extend the patent life of its product, have utterly manipulated the academic literature and clinical trials data in relation to the S and R enantiomers of citalopram. Although I have no evidence to back up my theory (because it seems like all of the academic research has been sponsored by Lundbeck/Forest Laboratories), from personal experience and intuition, I believe that R-citalopram is largely responsible for the anxiolytic properties of citalopram. If you read the academic literature about S-citalopram and R-citalopram, they all mention that R-citalopram counteracts the "antidepressant and anxiolytic" properties of S-citalopram based 5HT release in the frontal cortex. This is entirely disingenuous because it does not mention other potential modes of action that R-citalopram has on other neurotransmitter systems, such as gamma-Aminobutyric acid (GABA), for example.
What are your thoughts?