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Why would this D2 receptor agonist cause sleepiness? This is a side effect of L-dopa, also a D receptor agonist. Seems to me it should perk you up.
i thought dopamine has this type of effect on its own? and that its only when it turns into norepinephrine that it turns activating....I can tell this difference between when I take Vyvanse (pure dexamp) and Adderall (dex-amp and lev-amp)
As I understand it DA is the neurotransmitter most closely associated with alertness, but D receptors are widely spread thru theout body and there are a lot of types with different effects.
For sure Epi, NE and DA are very similar structurally and are somewhat interconvertable. As for the dextro and levo: these chemicals are 3 dimentional as compared to a water molecule, fer instance, which is 2D. Any given 3D molecule can have 2 structures- just like a right hand and a left hand do. They are identicall as far as their constituants and structure go- but they are mirror images of each other and as such not have the same bioactivity. The L form of amino acids and the D form of sugars (primarily glucose) are usually the biologically reactive form.
Here is the big picture:
Isomer - Wikipedia, the free encyclopedia
Levorotation and dextrorotation - Wikipedia, the free encyclopedia
Racemization - Wikipedia, the free encyclopedia
As I understand it DA is the neurotransmitter most closely associated with alertness, but D receptors are widely spread thru theout body and there are a lot of types with different effects.
For sure Epi, NE and DA are very similar structurally and are somewhat interconvertable. As for the dextro and levo: these chemicals are 3 dimentional as compared to a water molecule, fer instance, which is 2D. Any given 3D molecule can have 2 structures- just like a right hand and a left hand do. They are identicall as far as their constituants and structure go- but they are mirror images of each other and as such not have the same bioactivity. The L form of amino acids and the D form of sugars (primarily glucose) are usually the biologically reactive form.
Here is the big picture:
Isomer - Wikipedia, the free encyclopedia
Levorotation and dextrorotation - Wikipedia, the free encyclopedia
Racemization - Wikipedia, the free encyclopedia