The effect of caffeine is biologically mediated by cyclic AMP (adenosine 5'-monophosphate cyclical) in a combined action on two levels:

Cyclic AMP Abbreviation for cyclic adenosine monophosphate.

Adenosine plays an important role in biochemical processes, such as energy transfer - as adenosine triphosphate (ATP) and adenosine diphosphate (ADP) - as well as in signal transduction as cyclic adenosine monophosphate, cAMP.

This process is instigated through the fact that forskolin increases the cellular levels of a compound called cyclic adenosine monophosphate, or cAMP.

The principal mechanism through which it accomplishes this is enhancing the cellular degrees of a compound called cyclic adenosine monophosphate, or cAMP.

This process is instigated by the fact that forskolin increases the cellular levels of a compound called cyclic adenosine monophosphate, or cAMP.

It increases cellular levels of cyclic adenosine monophosphate (cAMP), the knock-on effect of which is increased fat-burning and some protein synthesis.

Liraglutide action is mediated via a specific interaction with GLP-1 receptors, leading to an increase in cyclic adenosine monophosphate (cAMP).

One of the most interesting, researched and prospectively helpful is its it’s ability to promote healthy cells through the enzyme Cyclic Adenosine Monophosphate (cAMP).

According to the ForskolinFit Pro website, forskolin works by using the messenger cAMP (Cyclic Adenosine Monophosphate) to activate enzymes that burn existing fat.

One of the most interesting, researched and prospectively helpful is its ability to promote healthy cells through the enzyme Cyclic Adenosine Monophosphate (cAMP).

The present invention provides a fast, cost effective, reliable method for the detection and quantification of cyclic-di-adenosine monophosphate (c-di-AMP) by measuring c-di-AMP binding to a c-di-AMP-binding protein (CabP).

But other intracellular messengers such as cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) are also involved (see the section Principles of drug action).

This increases cAMP levels, especially in inflammatory cells where PDE4 is the dominant enzyme responsible for breaking down cAMP.

Receptors for CRH are present in the myometrium, but the mechanism of action of CRH should not cause contraction, but the relaxation of the myometrium, since CRH increases cAMP (intracellular cyclic adenosine monophosphate).