Some receptors remain unoccupied even when an agonist produces a maximal response. Such empty ones are called spare receptors. In presence of spare receptors the maximum effect of an agonist drug is achieved with fewer than 100% of the receptors being occupied. To determine the presence of spare receptors, scientists often compare the concentration of the drug needed to produce 50% of the maximum effect (EC50) with the concentration of the drug needed to occupy 50% of the receptors (Kd). If the EC50 is smaller than the Kd, spare receptors are said to be present.
Spare receptors act as functional reserves and allow cells to economically use endogenous agonists such as hormones and neurotransmitters.
The presence of spare receptors is indicated by two mechanisms that amplify signal duration and intensity.
The availability of these surplus receptors increases the cell's sensitivity toward the agonist. Cells are sensitive to a small change in insulin levels because 99% of them are spare. This indicates that only a small fraction of activated insulin receptors are enough to allow glucose uptake and meet the energy requirement of cells.
These spare receptors make a small amount of agonist more effective. At the same time, these receptors indicate that a higher concentration of antagonist is needed to diminish the agonist's effect. In the example of insulin receptors, even in the presence of insulin, 99% of receptors are unoccupied. To counteract insulin's response, the antagonist also needs to occupy these 99% spare receptors, indicating the need for higher antagonist concentration compared to the agonist. In contrast, the heart has only 5% to 10% of spare β-adrenoceptors, indicating that a low amount of β-blockers is sufficient to revive a failing heart.
Typically, agonists generate maximal biological response by binding only some of the total available receptors. The unoccupied ones are called spare receptors.
Spare receptors can result from two mechanisms. In some pathways, one agonist-receptor complex interacts with many intermediary protein molecules to activate multiple effector molecules. So, the number of receptors exceeds the available effector molecules, leaving many receptors spare.
In other cases, even after the agonist-receptor complex disassembles, the activated intermediary proteins keep interacting with the effector proteins. As a result, only a few activated receptors are enough to evoke a maximal response, leaving the rest unused.
Such mechanisms allow the cell to use a low concentration of endogenous agonists, such as hormones and neurotransmitters, to produce the full response.
For example, 99% of insulin receptors are spare. The remaining are activated at low insulin concentration, maintaining blood glucose levels around the clock.
Spare receptors also increase the cell's sensitivity to agonist drugs as the chances of drug-receptor interaction increase in a large receptor pool.
繁體中文
