Exam 4: Stabilizing Long-Term Potentiation

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Describe how actin filaments are broken down into smaller units. Why is this beneficial?

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Myosin IIb motor proteins use actin as tracks, and when they move, they exert a shearing force, breaking filaments into smaller segments. In its unphosphorylated state, cofilin severs actin filaments. These segments then can be used to assemble filaments elsewhere in the spine.

In its non-phosphorylated state cofilin can sever actin filaments.

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Drugs like latrunculin and cytochalasin prevent actin polymerization.

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What is a benefit of larger spines?

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Inhibiting the activity of myosin IIb prevents enduring _______ but has no effect on its _______.

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When actin polymerization is inhibited the actin cytoskeleton will enlarge.

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Which action(s) influence(s) LTP stabilization but not induction? (Select all that apply.)

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In Harou Kasai's study of single spine enlargement, what was the effect of antagonizing NMDA receptors?

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Applying drugs that inhibit myosin IIb prior to TBS prevents the induction and stabilization of LTP.

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In its inactive state CaMKII _______ actin filaments.

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Briefly describe how the delivery of low-frequency stimulation prior to induction of LTP affects its generation and its stabilization.

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What is an "adhesive zipper"?

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Which statement(s) support(s) the hypothesis that actin polymerization is critical to stabilizing LTP? (Select all that apply.)

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_______ phosphorylates cofilin.

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In its normal non-phosphorylated state, cofilin _______. (Select all that apply.)

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Low-frequency stimulation delivered 15 minutes after LTP induction has no effect on stabilization

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Which statement(s) is/are true? (Select all that apply.)

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The stabilization of LTP depends on the reorganization of N-cadherins, but the generation of it does not.

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In Harou Kasai's study of single spine enlargement, what was the effect of the actin polymerization inhibitor, latrunculin

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In its active state, LIMK _______ cofilin.

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