FAQ/Help |
Calendar |
Search |
Today's Posts |
|
06-12-2017, 06:44 PM | #1 | ||
|
|||
Senior Member
|
As I understand it, there are two distinct mechanisms which have been used to reduce the peripheral metabolism of levodopa:
- DDC inhibitor (e.g carbidopa). Carbidopa [1] "inhibits aromatic-L-amino-acid decarboxylase (DOPA decarboxylase or DDC), ... an enzyme important in the ... biosynthesis of L-DOPA to dopamine (DA). DDC exists both outside of (body periphery) and within the confines of the blood brain barrier." - COMT inhibitor (e.g. entacapone). Entacapone [2] "is a selective and reversible inhibitor of the enzyme catechol-O-methyltransferase (COMT)... When taken together with levodopa (L-DOPA) and carbidopa, entacapone stops catechol-O-methyltransferase from breaking down and metabolizing levodopa, resulting in an overall increase of levodopa remaining in the brain and body." So, there's Sinemet (= levodopa + carbidopa) and Stalevo (= levodopa + carbidopa + entacapone). But, I've never seen levodopa + entacapone (i.e. without carbidopa). Why is this? References: [1] Carbidopa - Wikipedia [2] Entacapone - Wikipedia John
__________________
Born 1955. Diagnosed PD 2005. Meds 2010-Nov 2016: Stalevo(75 mg) x 4, ropinirole xl 16 mg, rasagiline 1 mg Current meds: Stalevo(75 mg) x 5, ropinirole xl 8 mg, rasagiline 1 mg Last edited by johnt; 06-12-2017 at 06:50 PM. Reason: typo |
||
Reply With Quote |
06-12-2017, 08:35 PM | #2 | ||
|
|||
Member
|
My understanding regarding DDC inhibitors is as follows:
- if you don't add a DDC inhibitor (i.e. carbidopa/benserazide), you need to use a much larger dose of levodopa, in order for sufficient levodopa to make it into the brain; - such large doses of levodopa cause unwanted side effects (e.g. nausea). My understanding regarding COMT inhibitors is that their main function (in PD treatment) is to (try to) stop COMT from breaking down dopamine in the brain. |
||
Reply With Quote |
"Thanks for this!" says: | johnt (06-13-2017) |
06-13-2017, 02:37 AM | #3 | ||
|
|||
Senior Member
|
Jeffreyn,
Thanks for your prompt reply. I agree when you write: "- if you don't add a DDC inhibitor (i.e. carbidopa/benserazide), you need to use a much larger dose of levodopa, in order for sufficient levodopa to make it into the brain; - such large doses of levodopa cause unwanted side effects (e.g. nausea)." You write: "My understanding regarding COMT inhibitors is that their main function (in PD treatment) is to (try to) stop COMT from breaking down dopamine in the brain." I'm not familiar with this process. However, what you describe is the role played by MAO-B inhibitors (e.g. rasagiline) [1]. "Selective MAOB inhibitors ... preferentially [inhibit] MAOB, which mostly metabolizes DA. If MAOB is inhibited, then more DA is available for proper neuronal function, especially in Parkinson's Disease. In a recent doctorial thesis [2] I've found a reference to the effect of levodopa plus entacapone without carbidopa: "That the Cmax and AUC of levodopa in both CSF and blood increased significantly when additional entacapone was given alone and in combination with carbidopa. The increase was more evident when entacapone was combined with carbidopa." Reference: [1] Monoamine oxidase B - Wikipedia [2] "Levodopa pharmacokinetics-from stomach to brain" Maria Nord, Dissertation, Linkoping University, 2017 https://liu.diva-portal.org/smash/ge...FULLTEXT01.pdf John
__________________
Born 1955. Diagnosed PD 2005. Meds 2010-Nov 2016: Stalevo(75 mg) x 4, ropinirole xl 16 mg, rasagiline 1 mg Current meds: Stalevo(75 mg) x 5, ropinirole xl 8 mg, rasagiline 1 mg |
||
Reply With Quote |
"Thanks for this!" says: | jeffreyn (06-13-2017) |
06-13-2017, 08:37 AM | #4 | ||
|
|||
Member
|
John, it's not just levodopa that the COMT enzyme acts on, it's all the catecholamines as well.
From Wikipedia (see link): "Catechol-O-methyltransferase (COMT) is one of several enzymes that degrade catecholamines (such as dopamine, epinephrine, and norepinephrine), catecholestrogens, and various drugs and substances having a catechol structure." Catechol-O-methyl transferase - Wikipedia In regards to your main point, if you had a drug which contained just levodopa and entacapone, you wouldn't be able to stop the DDC enzyme from converting a lot of the levodopa into dopamine, before the levodopa made it into the brain. The dopamine produced in this way would be of no benefit to the PwP, since dopamine cannot pass through the blood-brain barrier. |
||
Reply With Quote |
06-13-2017, 09:21 AM | #5 | ||
|
|||
Magnate
|
i don't think carbidopa and entacapone pass the BBB. if carbidopa entered the brain very little l-dopa would be converted to dopamine in the brain. this feature made carbidopa so attractive and reduced the l-dopa dosage from over 10grams and impractical to use to treat pd for the masses to what it is today.
entacapone also doesn't cross the BBB which makes it less potent than Tolcapone (tasmar) which i think is no longer used in the U.S. over liver toxicity risks and the need to monitor that. Medscape: Medscape Access Entacapone is highly protein bound, approximately 98%, with a limited body distribution.[42,44] It has poor brain penetration and predominately peripheral effects, although it may exhibit central effects if given in high doses.[ |
||
Reply With Quote |
06-13-2017, 10:54 AM | #6 | ||
|
|||
Member
|
ST is correct, entacapone has limited ability to pass the BBB. Tolcapone had significantly better absorption in both the body and brain.
|
||
Reply With Quote |
"Thanks for this!" says: | jeffreyn (06-13-2017) |
Reply |
|
|
Similar Threads | ||||
Thread | Forum | |||
Pain-RX - Cox 2 Inhibitor | Vitamins, Nutrients, Herbs and Supplements | |||
LRRK2 inhibitor may slow progression for all PWPs | Parkinson's Disease | |||
Ace inhibitor? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Common Herbs With MAO Inhibitor Activity | Parkinson's Disease | |||
FP0011 can be a potent, safe glutamate release inhibitor | Parkinson's Disease |