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Compositional changes, hydrophobic tail

The answer is E. Anesthetics are highly lipid-soluble and experiments with isolated membranes indicate that these molecules can dissolve in the hydrophobic center of the membrane bilayer. This causes a measurable increase in the membrane fluidity by disrupting the packed structure of phospholipids tails. This is considered to be the main, direct mechanism by which this class of drugs inhibits neurotransmission (pain sensations) in neurons. Hallucinogens and opiates may also affect membrane fluidity, but their effects occur by indirect mechanisms, resulting from changes in the protein or lipid composition of the membranes. [Pg.50]


See other pages where Compositional changes, hydrophobic tail is mentioned: [Pg.113]    [Pg.14]    [Pg.2843]    [Pg.557]    [Pg.266]    [Pg.115]    [Pg.296]    [Pg.115]    [Pg.61]   


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Composition change

Hydrophobic tail

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