Jennifer Lynne Whistler

The paper examines how gut microbiota changes in mice with addiction-like behavior, finding that compulsive morphine use leads to stable dysbiosis while non-compulsive mice show more flexible microbial adaptation.

This study identifies D3R-expressing neurons in the NAc as mediators of quetiapine's aversive effects, showing that chronic treatment reduces this aversion.

The paper identifies microbiota-driven butyrate production as a factor maintaining antinociception in mice resistant to morphine tolerance.

This study shows that GASP1-mediated GLP-1R trafficking contributes to tolerance to incretin drugs, suggesting a strategy to prevent tolerance by biasing drug engagement toward G protein signaling.

This study examines dopamine release in the medial and lateral shell of the nucleus accumbens in response to acute and chronic morphine exposure in mice, revealing distinct responses between the two sub-regions.

This study identifies some second generation antipsychotics (SGAs) as arrestin-3 agonists at D3 dopamine receptors, showing that chronic use leads to receptor degradation and altered drug efficacy.