Give typed explanation another type of antidepressant inhibits the enzymes that naturally break down seritonin at the synaptic cleft. can you explain how this might reduce the symptoms of depression?
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Give typed explanation
another type of antidepressant inhibits the enzymes that naturally break down seritonin at the synaptic cleft. can you explain how this might reduce the symptoms of depression?
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- Parkinson's Disease Parkinson's disease is neurodegenerative disorder that affects movement. Most people affected with Parkinson's disease demonstrate rigidity, slow movement, and shaking. The symptoms of Parkinson's disease occur when the cells that produce dopamine neurotransmitters die in the brain. Explain how the signal transmission at a synapse in an individual with Parkinson's disease is different than an unaffected individual. Describe the normal process of signal transmission at a synapse. Start with the arrival of an action potential at the axon terminal and include the name of the neurotransmitter that is affected by Parkinson's disease. Explain how the process is different in individuals affected with Parkinson's disease.Explain how the binding of heroin to presynaptic neurones raises the probability of action potentials in the postsynaptic neurone. asap typed onlySelective serotonin reuptake inhibitors (SSRIs) are drugs that can alleviate symptoms of depression by blocking the reuptake of serotonin (5-HT) from the synaptic cleft, thereby increasing the amount of time that 5-HT remains active. Elevated levels of 5-HT within the synapse are associated with feelings of well-being; conversely, low levels of 5-HT are correlated with depressive symptoms. Recent studies have shown that SSRIs can also mediate their antidepressant effects by increasing brain levels of certain cytokines, including interferon gamma (IFNY). IFNY directly induces the expression of the protein p11 in neighboring neurons, which then interacts with 5-HTR4, a 5-HT transmembrane receptor. Figures 1 and 2 provide information about this interaction. 5-HTR4 protein (% of WT) expression CAMP levels (% change control) from 120T 100+ 80+ 60+ 40+ 20+ 0 MEM TOT Figure 1 5-HTR4 protein expression in plasma membrane-enriched fraction (MEM) of hippocampal lysate and in total hippocampal…
- Drugs that block dopamine synapses tend to impair or slow limb movements. However, after people have taken such drugs for a long time, some experience involuntary twitches or tremors in their muscles. Based on material in this chapter, propose a possible explanation.Serotonin, norepinephrine, and dopamine are a group of neurotransmitters collectively called monoamines. A lack of these monoamines has been linked to depression. Depression is treated with dru that prolong the effect of these neurotransmitters either by preventing the re-uptake of the neurotransmitters, or by inhibiting the enzyme that breaks down these neurotransmitters. Which of the following statements about neurotransmitters'are true? The table lists the classifications of three antidepressants. Antidepressant Classification fluoxetine selective serotonin re-uptake inhibitor (SSRI) phenelzine monoamine oxidase (MAO) inhibitor amitriptyline tricyclic antidepressant Check all that apply. View Available Hint(s) MAO inhibitors are examples of monoamine antagonists. EFluoxetine inhibits the enzyme that breaks down monoamines. ODopamine plays a role in feelings of pleasure and pain. DA deficiency of serotonin norepinephrine, and dopamine is associated with depression. Some drug…In a cell line derived from normal rat thyroid, stimulation of the alpha1-adrenergic receptor increases both IP3 formation and release of arachidonic acid (AA). IP3 elevates cytosolic Ca, which mediates thyroxine efflux, whereas AA serves as a source of prostaglandin E2, which stimulates DNA synthesis. It is not clear how AA release is connected to the adrenergic receptor. AA could arise by cleavage from the DAG that accompanies IP3 production. Alternatively, AA could arise through an independent effect of the receptor on PLA2, which can directly release AA from intact phosphoglycerides. Consider the following experimental observations: a) Addition of noradrenaline to cell cultures stimulates production of both IP3 and AA. b) If the alpha1-adrenergic receptors are made unresponsive to noradrenaline by treatment with phorbol esters (which act through PKC to cause phosphorylation, and inactivation, of the receptor), addition of noradrenaline causes no increase in IP3 or AA. c) When…
- Changes in intracellular Ca2+ is one of the main governing factors that determines the direction of plasticity (i.e., whether a synapse potentiates or depresses). Provide a general mechanism to explain how changes in intracellular Ca2+ can result in either synaptic depression or synaptic potentiation (refer to our discussion on kinases and phosphatases).Describe in detail the proposed mechanism of action of the experimental anti-Parkinsonian drug Prosavin.What is the mechanism of LTP expression? Select one: a. Increase in the number of postsynaptic NMDA receptors b. Increase in the intracellular level of proteins involved in synaptic release c. Increase in the number of postsynaptic AMPA receptors d. Increase in the number of presynaptic AMPA receptors e. Decrease in the level of glutamate released into the synaptic cleft
- One of the initial symptoms a person can have for COVID-19 is the lost of taste and smell. Give a potential mechanism, including which portion of the reflex arc is being impacted, of how COVID is able to have this impact. Use an online source to support your argument.discuss the excitatory NMDA receptor, the role of the Mg++ ion, and how NMDA activation can produce Long Term Potentiation (which could underlie memory). Finally, what is the seemingly unique involvement of neighboring glia cells in helping to regulate both GABA and Glutamate neurotransmission and why might that glia cell role occurMalathion is an insecticide commonly used in the horticultural industry. Many homeowners apply this chemical to their trees to rid them of infestation by aphids or other insects. Malathion is classified as an organophosphate insecticide. Exposure to malathion is very dangerous to humans and animals because it acts as an irreversible inhibitor of acetylcholinesterase. Predict what might happen to synaptic communication between cholinergic neurons if an individual or animal was poisoned with malathion, and clearly describe the mechanisms at work.