Linear and inverted U-shaped dose-response functions describe estrogen effects on hippocampal activity in young women.
Janine BayerJan GläscherJürgen FinsterbuschLaura H SchulteTobias SommerPublished in: Nature communications (2018)
In animals, 17-beta-estradiol (E2) enhances hippocampal plasticity in a dose-dependent, monotonically increasing manner, but this relationship can also exhibit an inverted U-shaped function. To investigate E2's dose-response function in the human hippocampus, we pharmacologically increased E2 levels in 125 naturally cycling women (who were in their low-hormone menstruation phase) to physiological (equivalent to menstrual cycle peak) and supraphysiological (equivalent to levels during early pregnancy) concentrations in a placebo-controlled design. Twenty-four hours after first E2 intake, we measured brain activity during encoding of neutral and negative pictures and then tested recognition memory 24 h after encoding. Here we report that E2 exhibits both a monotonically increasing relationship with hippocampal activity as well as an inverted U-shaped relationship, depending on the hippocampal region. Hippocampal activity exhibiting a U-shaped relationship inflects at supraphysiological E2 levels, suggesting that while E2 within physiological ranges stimulates hippocampal activity, supraphysiological ranges show opposite effects.
Keyphrases
- cerebral ischemia
- temporal lobe epilepsy
- brain injury
- endothelial cells
- subarachnoid hemorrhage
- blood brain barrier
- type diabetes
- working memory
- estrogen receptor
- physical activity
- radiation therapy
- pregnant women
- body mass index
- cognitive impairment
- adipose tissue
- skeletal muscle
- insulin resistance
- pregnancy outcomes
- neural network
- phase ii
- phase ii study