Chapter 26: Problem 2
What is the difference between parkinsonian syndrome and Parkinson's disease?
Chapter 26: Problem 2
What is the difference between parkinsonian syndrome and Parkinson's disease?
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Get started for freeRegarding the cytotoxicity of inflammation, which statement is not correct? a. Both oxygen and nitrogen reactive species can participate in the deleterious effects of inflammation. b. Inactivation of NADPH-oxidase, but not of nitric oxide synthase matigates MPTP-induced neurodegeneration in mice. c. The detrimental effects of inflammation on dopaminergic neurons can be mediated by soluble factors. d. Astrocytes and microglial cells can mutually modulate their degree of activation. e. Dopaminergic neurons express receptors for various deleterious cytokines.
Which statement about experimental models of Parkinson's disease is true? a. Both genetic and toxic models exist, but only the former are commonly used. b. Inflammation has been described in all popular models of Parkinson's disease. c. The MPTP monkey model suggests that an acute intoxication produces an acute neurodegenerative event that is completed in a few days. d. The MPTP mouse model suggests that the toxin peosokes inflammation, which, in turn, kills dopaminergic neurons. e. Neuronophagia which suggests ongoing inflammation has been described in genetics, but not in toxic models of Parkinson's disease.
Name the three theories about the detrimental role of inflammation in \(\mathbf{P D}\) and explain their respective basis.
Glial cells can exacerbate neurodegeneration in Parkinson's disease by? a. Losing their ability to assist neighboring neurons. b. Accelerating the demise of compromised neurons. c. A process of indiscriminate toxicity. d. Decreasing extracellular glutamate levels. e. \(\mathrm{a}, \mathrm{b}\) and \(\mathrm{c}\)
Which of the following glial functions may improve neuronal survival or regeneration? a. Inhibit phagocytos?s. b. Secrete chemotactic molecules to recruit polynuclear cells. c. Produce trophic factors. d. Assist in the synthesis of neuronal superoxide dismutase. e. Stimulate the formation of myelin to guide new axons.
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