Neuronal disorder and repair Flashcards

1
Q

What is Wallerian degeneration?

A

Active process of degeneration that results when a nerve fibre damaged and the part of the axon distal to the injury degenerates.

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2
Q

What do oligodendrocytes required to survive?

A

Oligodendrocytes require axon signals to survive.

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3
Q

What happens to oligodendrocytes in injury?

A

Upon injury, the oligodendrocytes fail to clean up the myelin sheaths and their debris - glial scar formation -inhibits regeneration and reinnervation.

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4
Q

What is Vincristine peripheral neuropathy?

A

Vincristine = chemotherapy medication required to treat a number of types of cancer.

Vincristine works by binding to the tubular protein, stopping tubular dimers from polymerising to form microtubules. In cancer treatment stops chromosome separation and leads to apoptosis.

Symptoms of neuropathy are mainly sensory - pain, tingling and numbness. Sometimes motor nerves and ANS involvement. Thought that microtubule disturbance in nerves = cause.

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5
Q

What is neuropraxia?

A

Transient block (no degeneration and minimal lesion) recovers completely and rapidly

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6
Q

What is axonotmesis

A

Damage causes degeneration, but the nerve supporting structure remains

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7
Q

What is neurotmesis

A

Complete anatomical division of the nerve

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8
Q

Can the PNS regenerate?

A

Yes,

Schwann cells dedifferentiate and upregulate production of both neurotrophic factors and growth promoting ECM.

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9
Q

What happens when there is CNS damage?

A

Mechanical injury to the adult mammalian CNS always results in the formation of a lesion scar: a regeneration barrier.

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10
Q

What happens to the BBB in CNS damage?

A

BBB breakdown

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11
Q

What is the inflammatory response in response to CNS damage?

A

Recruitment of neutrophils
Recruitment of microglia cells/ macrophages, surrounding tissue accumulates with neutrophils, microglia, increased cytokines, induced inflammatory response and induced degeneration.

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12
Q

What factors stimulate glial scar formation?

A

Inflammatory factors .

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13
Q

What constitutes the glial scar?

A

Astrocytes, microglia and oligodendrocyte progenitor cells

mainly astrocytes

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14
Q

What is a fibrotic scar consistent of? How?

A

Fibrotic scar formed by fibroblasts, which have invaded the lesion site from adjacent meningeal and perivascular cells.

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15
Q

What is a theory about the impact of glial scars on healing?

A

Failure to regenerate is due to the blocking effect of the scar formed at the lesion site.

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16
Q

What do reactive astrocytes and fibroblasts form at the scar interface? What is its role?

A

Glia limitans - protective in reconstituting the BBB, preventing neuronal degeneration and limiting the spread of damage

17
Q

What two ways do scars inhibit regeneration?

A

Physically and chemically

18
Q

How do scars inhibit regeneration chemically?

A

Inhibiting factors upregulated prevent regrowth (Chondroitin sulfate proteoglycan (CSPG) family, tenascin, semaphorin 3A, myelin-associated molecules and subtypes of the Eph receptors and their ligands ephrins)

19
Q

How do scars inhibit regeneration physically?

A

Transected axons stop at the border of the fibrotic scar due to its complex, densely packed structure

20
Q

What are neurotrophic factors?

A

Neurotrophic factors promote survival and growth of neurons.

21
Q

What effects do neurotrophic factors have?

A

autocrine and paracrine - promote neuron growth and glial growth

22
Q

How does neuronal cell death occur in CNS damage? (two ways)

A

Either from neurotoxicity - excess glutamate causes Ca2+ influx and cell death.

Or axotomy prevents neurotrophic retrograde transport so neutrons die.

23
Q

What cells make neurotrophic factors?

A

Schwann cells

24
Q

Cell therapy: possible application in Parkinson’s?

A

Can we exploit regeneration promoting PNS Schwann cells to repair CNS.

Use enzymes to remove the inhibitory side chains of CSPGs?

Inject neurotrophic factors.

Is neural transplantation an option?