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Receptor activation can happen within milliseconds to seconds when a ligand binds to the receptor, triggering a conformational change. The time it takes for the receptor to fully activate and initiate downstream signaling pathways can vary depending on the specific receptor and the cellular context.

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Drugs that increase receptor activation are those that?

Drugs that increase receptor activation are known as agonists. They bind to the receptor and produce a biological response. This can lead to a variety of effects depending on the specific receptor and drug involved.


The same receptor can have different effects depending on the properties of the?

ligand that binds to it. For example, a receptor can trigger different signaling pathways or cellular responses if it binds to different ligands, even if they bind to the same binding site on the receptor. This is known as ligand-dependent receptor activation.


What Cellular acetylcholine receptor is found in effector organs of the parasympathetic system?

The M2 muscarinic acetylcholine receptor is the primary receptor found in effector organs of the parasympathetic system. Activation of this receptor leads to inhibition of adenylate cyclase and decreased intracellular levels of cyclic AMP, resulting in various physiological responses in target tissues.


What is receptor desensitisation?

Receptors generate a cellular response upon binding their specific ligand. This response can vary in magnitude. Desensitisation is a phenomenon in which activation of a receptor can reduce the magnitude of the response if it is subsequently activated again. Usually the longer a receptor is activated for the greater the desensitisation will be. There are 3 general mechanisms as to how desensitisation occurs. The first is uncoupling of the receptor from proteins which generate the cellular response. The second is internalising receptors so that they cannot be activated. The third is reducing production of receptors so less are available. In general mechanism 1 is short term, 2 is mid-term and 3 is long term.


Primary opioid receptor is associated with analgesia?

The primary opioid receptor associated with analgesia is the mu-opioid receptor. Activation of the mu-opioid receptor by opioids such as morphine produces pain relief by modulating pain perception pathways in the brain and spinal cord. This receptor is also responsible for the euphoric effects of opioids, which can lead to their misuse and addiction.

Related Questions

Drugs that increase receptor activation are those that?

Drugs that increase receptor activation are known as agonists. They bind to the receptor and produce a biological response. This can lead to a variety of effects depending on the specific receptor and drug involved.


Activation of which kind of receptor causes heart rate to increase?

beta-one receptor


Which of the choices below is not a factor required for target cell activation by hormone receptor interaction?

Protein synthesis is not a factor required for target cell activation by hormone receptor interaction. The essential factors include binding of the hormone to its receptor, conformational changes in the receptor, and activation of intracellular signaling pathways.


The activation of receptor tyrosine kinases is characterized by?

The activation of receptor tyrosine kinases involves ligand binding to the extracellular domain, leading to receptor dimerization and autophosphorylation of tyrosine residues on the intracellular domain. This activation initiates downstream signaling cascades involved in cell growth, differentiation, and survival.


What membrane receptor undergoes dimerization and autophosphorylation?

Receptor tyrosine kinases (RTKs) are membrane receptors that undergo dimerization and autophosphorylation upon ligand binding. This activation leads to the recruitment and activation of downstream signaling molecules in the cell.


Is CD4 an adhesion molecule?

The glycoprotein CD4 is a co-receptor. A co-receptor is "a cell surface receptor, which, when bound to its respective ligand, modulates antigen receptor binding or affects cellular activation after antigen-receptor interactions." (MediLexicon)


When a signal molecule binds to a receptor protein the receptor protein may change the?

shape, leading to activation of signaling cascades within the cell. This activation can lead to changes in cell behavior or gene expression.


How does serotonin receptor down-regulation have an antidepressant effect if it results in a decrease in post-synaptic neuron activation?

The serotonin receptor down-regulation has an antidepressant effect if it results in a decrease in post-synaptic neuron activation by activation of the 5-HT receptors within the rostral ventrolateral medulla.


The same receptor can have different effects depending on the properties of the?

ligand that binds to it. For example, a receptor can trigger different signaling pathways or cellular responses if it binds to different ligands, even if they bind to the same binding site on the receptor. This is known as ligand-dependent receptor activation.


How goserelin works on downregulation of gnrh?

Goserelin is an GnRH receptor agonist and bings stronger than GnRH. Due to the constant activation of the GnRH receptor (Goserelin binds really strong; Superagonist) the cell internalizes the receptor -> Downregulation.


The activation of receptor tyrosine kinases is characterized by what?

Receptor tyrosine kinases, when activated by ligand binding, undergo dimerization and autophosphorylation of tyrosine residues. This promotes the recruitment and activation of downstream signaling molecules, ultimately leading to a cellular response such as cell growth, differentiation, or survival.


What Cellular acetylcholine receptor is found in effector organs of the parasympathetic system?

The M2 muscarinic acetylcholine receptor is the primary receptor found in effector organs of the parasympathetic system. Activation of this receptor leads to inhibition of adenylate cyclase and decreased intracellular levels of cyclic AMP, resulting in various physiological responses in target tissues.