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organizational/activational hypothesis
developed to explain how hormones guide behavioral sex differences
behavioral sex differences result from:
differential exposure to hormones that act early in development to organize/program neural circuitry underlying sexually dimorphic behaviors
differential exposure to sex steriod homones later in life that activate the neural circuitry previously organized
young’s hypothesis
hormonal events early in development are important for adult reproductive behavior
young’s experiment
organizational: testosterone was given to pregnant guinea pigs (at levels that did not masculinize the genitalia of female offspring) and a control group (no hormone administration)
activational: as adults, hormone-treated and control female offspring were ovarectomized and given estrogen/progesterone (to stimulate female sexual behavior) and testosterone (to stimulate male sexual behavior)
young’s results
females exposed to androgens prenatally - behaved liked males
estrogen/progesterone administration: reduced female sexual behaviors
testosterone administration: exhibited male sexual behaviors
control females - behaved like females
estrogen/progesterone administration: exhibited female sexual behaviors
testosterone: no effect on sexual behaviors
young’s conclusion
potential for masculine or feminine behavior is organized by early exposure to androgens
distinction can be made between pre-natal actions of hormones in causing differentiation or organization of the neural substrates for behavior/actions of hormones in adulthood in causing activation of these substrates
sensitive/critical period
a period of time when an animal is maximally sensitive to organizing effects of hormones to permanently change morphology/behavior
once it is over, hormones do not have organizing effect
presence of androgens
permanently organizes the brain to permit later demonstrate masculine behavior in response to activational effects of hormones
brain is masculinized and defeminized
absence of androgens
the brain and behavior develop in a female typical fashion
brain is demasculinized and feminized
development
sensitive period
relatively permanent
characteristics of organization o
organization
hormones organize or program the neural circuitry underlying sexually dimorphic behaviors
adulthood
no sensitive period
transitory
characteristics of activational
activational
hormones act on the neural circuitry that was previously organized
aromatization
mechanism in rodents that masculinizes the brain
conversion of testosterone to estrogen/estradiol
alpha-fetoprotein
binds to estrogen and prevents maternal estrogen from mascuilinizing the female brain
cyclic
pattern of GnRH in females; without androgen exposurem the neural circuitry involved in GnRH surge generation is spared
tonic
pattern of GnRH in males; exposure to androgens in development abolishes the potential to generate GnRH surges
interuterine environment
maternal stress
materal care
environmental endocrine disruptors
environmental influences on mammalian sexual development
interuterine environment
in female rat pups’ position in the uterine horn can subtly impact her physiology and behavior as an adult → 2M females are more aggressive less attractive to males, have longer ovarian cycles
maternal stress
male offpring of mothers stressed during pregnancy act more feminine, possibly due to androgen production suppression
maternal care
males require maternal licking to develop normal adult sexual behavior
females who are licked more as pups are more attentive mothers as adults
endocrine disrupting chemicals
mimic the effects of hormones or disrupt hormonal systems can interfere with sexual differentiation
atrazine
commonly used herbicide; affect reproductve development in fish, amphibians, reptiles and mammals
estrogen
in birth control pills are excreted through urine, which enters the waste system. estrogen is too small to be filtered out of the sewage system, so it remains in drinking water
bisphenol A
BPA; used in synthesis of plastics; has estrogenic effects
triclosan
antibacterial that interferes with estrogen, androgen and thyroid hormones, increases the risk for breast cancer and decreases male fertility
PFAS
endocrine disrupting properties and are linked to neurodevelopment disturbances