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MAOA
produces enzyme MAOA (e-MAOA), which breaks down neurotransmitters like serotonin
these neurotransmitters regulate impulse control and emotional responses
MAOA-L have lower levels of MAOA, leading to a reduction in serotonin breakdown
during prenatal development, MAOA-L gene results in overexposure of brain to high serotonin levels which could cause the brain to be less receptive to serotonin in the future
which could impair emotional regulation and increase potential for aggression
animal models
used in research to understand humans without risk of causing harm to a human during the process, however there are still some ethical considerations that must be followed even with animal studies
animal models eval
Strengths
Allows for a longitudinal study across whole lifespan
Can rigorously control environment allowing for less extranious variables
Human study to support - meyer lindenberg
Limitation
Animals are different to humans in their cognitive levels meaning the results might not be generalised to the human population
meyer-lindenberg study of support
aimed to investigate how MAOA-L affects brain function
found that MAOA-L condition had significant increase of activity in amygdala and reduced activity in PFC
these results demonstrate a clear link between MAOA-L and increased aggression
cases aim
to investigate the genetic origins of aggression in mice
cases method
erased MAOA in mice and observed their actions
resident intruder paradigm was used where mouse placed inside cage of another mouse
also conducted an autopsy of the brain after observations
cases results
adult mice showed signs of aggressive behaviour like biting researcher
in intruder paradigm, mice without MAOA adopted a threatening stance when other mouse introduced and would exhibit aggressive behaviour while control would just sniff other mouse
brains of mice without MAOA had an increase in serotonin of 9 times higher than controls
cases conclusion
in conclusion, mice without MAOA showed more signs of aggression because they were more aggressive to intruders compared to mice with MAOA
TPH-2 knockout gene
converts tryptophan into serotonin
sends info to nucleus to begin process of conversion
if gene is deleted or reduced then that will reduce the serotonin levels in the brain
examined through animals where TPH-2 is knocked out (deleted)
Mosienko aim
to investigate how knocking out TPH-2 would affect mice
mosienko method
compared genetically modified mice with TPH-2 knocked out with control group
resident intruder test done
mosienko results
TPH-2 mice attacked 6 times faster than the control group when meeting the intruder
more TPH-2 knockout mice attacked intruder compared to normal mice
mosienko conclusion
in conclusion, TPH-2 knockout caused mice to become more aggressive compared to mice with TPH-2 still intact because the TPH-2 knockout mice attacked 6 times quicker than control group and conducted more attacks overall