Development/ROS Flashcards

1
Q

embryonic bilaminar disc

A

when implantation is occuring, the embyoblast develops a bilaminar embryonic disc –> epiblast and hydpoblast

completes at the end of week 2

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2
Q

prechordal plate

A

by day 14 -> thickening of the hypoblast, forms within the bilaminar disc, marking the cranial region of the embryo

important for oranganizing the dev of head region

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3
Q

general gastrulation def

A

the convserion of the bilaminar embryonic disc to a trilaminar which gives rise to the 3 germ layers – endo, meso, and ectoderm

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4
Q

tissues derived from the ectoderm

A

epidermis, nervous system, eye, innner ear, neualr crest cell –> connective tissues of the head

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5
Q

tissues derived from the mesoderm

A

skeletal muclses, blood cells, lining of blood vessles, viercerl small muscular caots, serosal linings, ducts and organs of the reporductive and exretory systems, most of cardiovascualr system, connective tissue of the trunk

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6
Q

tissues derived from the endodererm

A

epithelila lining of resp, digestive, reporductive and uriniary systems

glandular cells of assocaited organis (liver, pancreas, thymus, thyroid, and parathyroid glands)

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7
Q

gastrulation steps

A

e appearance of the primitive streak on the caudal end of of the epiblast

this streak is the thickening of the epiblast caused by the proliferation of epiblast between the epiblast and hypoblast –> organizing into the mesoderm

signaling moelcules like bone morphogenetic proteins (BMPs), Wnt and fibroblast growth factors (FGFs)

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8
Q

general neurlation

A

the process of the neural tube formation and closure

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9
Q

neuralation general steps

A

the CNA is formed form the neuroectoderm of the neural plate while the peripheral nevous sytem is derived fom the neuarl crest cells, the nural tube and mesoderm

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10
Q

1st 2nd and 3rd tirmester correlates to which daysin rodetns

A

1st- 1-10/11
2nd- 12- 21/22
3rd- PND 1-10

brian brain developemnt grows rapidly from week 25-38 weeks

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11
Q

teratogenesis and windows of suseptability

A

certain periods of embryonic or fetal development are more suseptiable to distruption than others

firt 2 weeks-> no effect or in utero death
emrbyonic period -> humans 4-8 weeks, mice GD 5-14 will result in strucutral birth defects, the specific type depend on the organ being developing
fetal period -> humnad week 9- birth, mice GD 14-19, results in functional defects like cognitive or motor defets, metabolic diseases like diabetes

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12
Q

reactive intermediate mediated mechanisms -> electrophili reactive intermediates bvs.

A

ex. benzo[a]pyrene

electrophillic reactive intermedaite-> structures have electron defient centers; ex. epxosides, bioactivation is usually catalzed by P450 CYPs

embryo has low levels of detoxifiying enzymes

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13
Q

reactive intermediate mediated mechanisms – free radical reactive intermediates

A

ex. phenyotin, methamphetamine, thalidomide, Etoh

bioactivation of xenobiotics to free radical intermediates

embryo expresses high levels of PHS and lipoxygenases but low levels of CYP enzymes

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14
Q

ROS types - superoxide anion

A

one electron reduction of O2

can react with nitric oxide to make peroxynitire

can be converted to H2O2 enzymatically by SOD

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15
Q

ROS types: H2O2

A

non radical

can easily cross biological membranes,

removed by catalase or by glutathione peroxidases

fenton reaction –> reacts with iron or copper metals to make hydroxy radicals

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16
Q

ROS types

hydroxyal radical

A

3 electron reduction of oxygen

very short half life 10^-9 and dose not diffuse from the site of generation

damage to protins leads to loss of activity, damage to lipids can lead to lipid peroxidation

17
Q

endogenous sources of ROS

A

MTC - oxidative phosphorylation, ROS can be formed through the electron transfers, 5% of electrons that go through complex 1 and 3 ae diverted to superoxide, but the mitochondria have high levels of SOD

ER contains CYP enzymes
peroxisomes
NADPH oxidases

xanthine oxidases
auto oxidation of small molecules liek dopamine

18
Q

mouse brain development - neurulation

A

neural tube formation -> finished GD 10-11

○ PAE specifically effects the neurulation

19
Q

mouse brain development - neurogenesis

A

Neuogenesis and cell migration for forebrain, midbrain and hindbrain -> starts GD 5-11

20
Q

mouse brain development - GD 11-21

A

most CNS areas have distinct differentiation processes and several neuronal cell types emerge and migrate to specific parts of the brain
PAE effect prolication and migration processes of the neocortex, cerebellum, hippocampus and basal ganglia

21
Q

mouse brain development - GD 18- PND 9

A

prolifation of astroglia and oligofendroglial cells, synaptogenesis, and dendritic arborization
○ Alochol exposure results in sever nuronal loss, reactive fliosis, impaired myelination and damage to prefrontal cortex, hippocampal and cerebellar regions

22
Q

• What is the definition of oxidative stress

A

o Oxidative stress was originally defined as an imbalance between ROS and antioxidant defence mechanisms, but the definition has been recently modified, recent version –> imbalance between oxidant and antioxidants in faou of the oxidants, leading to a disruption of redox singling and control and or molecular damage