y Day 3 of Week 1
Post a response answering the following:
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Write My Essay For MeExplain the difference between ion channels and G proteins as they relate to signal transduction and targets of medications.
How would you answer the following patient question:
My grandmother has a mental illness. I have the same genes as her. Will I also get the same mental illness?
Note: Your response needs to be supported and validated by three (3) scholarly peer-reviewed resources located outside of your course Learning Resources.
Q one response.
Ion channels and G protein-coupled receptors (GPCRs) are two major classes of proteins responsible for membrane signaling and are also drug targets. Similar to all membrane proteins, ion channels and GPCRs interact with lipids in cell membranes. These interactions may be of two types: interactions with the lipid bilayer as a hydrophobic environment of a certain thickness and fluidity, which exerts lateral pressure, or specific interactions of lipids as ligands. The latter interaction type has the potential to act as allosteric regulatory ligands of membrane proteins and thus offer potentially druggable sites (Duncan et al., 2020).
Ion channels, for instance, are responsible for ion fluxes and electrical excitability within the nervous system and elsewhere. Several phospholipids, particularly phosphatidylinositol 4,5-bisphosphate (PIP2) (Suh, 2008; Hansen, 2015; Duncan et al., 2020) and cholesterol (Levitan et al., 2014; Duncan et al., 2020), bind to and regulate ion channels (Duncan et al., 2020). When these ion channels are used, the electrical state of the cell alters, contributing to the process, such as when they open and close to regulate flow, leading to the cell’s composition and membrane potential.
On the other hand, g protein-coupled receptors (GPCRs) are the largest and most diverse group of membrane receptors in eukaryotes. They are activated by a wide variety of ligands in the form of light energy, lipids, sugars, peptides, and proteins (Billington & Penn, 2003: Schoneberg et al., 2004; lundstrom, 2009; Ahmad & Dalziel, 2020) which convey information from the outside environment into the cell to mediate their corresponding functional responses. The conformational changes of GPCRs upon ligand binding initiate a series of biochemical reactions within the cell, leading to a physiological response.
Q two response.
As a provider, you must take into consideration all factors that may affect a response, and the question about genes and their link with mental illness and mental health is complex. It may include the content of genetics, personal situations, and environmental factors. In responding to the client’s concern, genetics and mental health issues may be addressed. Still, the fact that it may run in the family may increase the risk but does not warrant the definite chance of having the disorder/disease, as other factors may play a significant role. This can include environmental factors, which may impose a stressful mark on your being, leading to increased risk. That is why it is so important to manage your life effectively by managing those stressors that may be affecting you. Attempt to be proactive with your health, seek early treatment, and seek preventive care, as this allows for timely intervention, resource optimization, reduced stigma, personalized treatments, and enhanced understanding of mental health, therefore promoting prevention and holistic well-being (Jayakumar & Reshman, 2024)
Reference
Ahmad, R., & Dalziel, J. E. (2020). G protein-coupled receptors in taste physiology and pharmacology. Frontiers in pharmacology, 11, 587664.
Duncan, A. L., Song, W., & Sansom, M. S. (2020). Lipid-dependent regulation of ion channels and G protein-coupled receptors: insights from structures and simulations. Annual review of pharmacology and toxicology, 60, 31-50.
Jayakumar, N., & Reshma, N. (2024, February). Modeling Mental Health: Advances in Predictive Science towards Proactive Health Care. In 2024 IEEE International Conference for Women in Innovation, Technology & Entrepreneurship (ICWITE) (pp. 202-206). IEEE.
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