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Jack Bergman

Harvard Medical School, McLean Hospital, Belmont, Massachusetts.

5 papers in the library · 10 citations · publishing 2018-2026

Papers

Environmental determinants of ketamine's prohedonic and antianhedonic efficacy: Persistence of enhanced reward responsiveness is modulated by chronic stress.

The Journal of pharmacology and experimental therapeutics May 1, 2025 Amaya R Jenkins, Daniela B Radl, Thomas J Kornecook et al. 8 citations

Ketamine produces short-lived increases in reward responsiveness in rats under nonstressful conditions, but under ongoing chronic stress it rescues blunted reward responsiveness for nearly one week. These findings highlight the role of environmental context in ketamine's effects on reward processing and suggest its antianhedonic action may contribute to its antidepressant efficacy.

Chronic Δ9-tetrahydrocannabinol exposure during adolescence is associated with persistent behavioural tolerance in adult nonhuman primates.

British journal of pharmacology November 1, 2025 Yasaman Razavi, Stephen J Kohut, Jack Bergman et al. 1 citation

Adolescent monkeys exposed daily to the cannabis compound Δ9-THC for six months, then tested about a year later as adults on a touchscreen attention task, required higher acute doses of Δ9-THC to impair their performance compared with animals that had not been exposed during adolescence. The impairment itself was dose-related and occurred whether the drug was given by injection or orally, though potency and timing differed. These results suggest that heavy cannabis use during adolescence can produce a lasting tolerance that persists into adulthood, even after a long period of abstinence.

2018/7/6/curcumin-breast-cancer-therapeutic-agent-to-replace-allopathic-treatments-with-extensive-side-effects

July 9, 2018 Chu Hsien Lim, Brian D. Kangas, Jack Bergman 1 citation

Cancer patients face elevated rates of depression and anxiety, often leading to worse healthcare outcomes. Given limited treatment options, interest has grown in using psychedelics like psilocybin to manage these complications. Recent studies have shown the potential of psilocybin to alleviate depression and anxiety in cancer patients.

Psychedelics produce enduring enhancement of reward responsiveness in male rats

Neuropsychopharmacology July 10, 2026 Christopher W. Thomas, Kayleigh S. Lamalfa, Tobias P. Whelan et al.

Psilocybin and ketamine acutely increased reward responsiveness in rats, and the effect persisted 24 hours after dosing. The increase from psilocybin, but not ketamine, was blocked by a 5-HT2A receptor antagonist. Other psychedelics, DMT and DOI, also acutely increased reward responsiveness but the effect did not last 24 hours. The non-psychedelic 5-HT2A agonist lisuride and the SSRI fluoxetine had no positive effects. These results suggest psychedelics can produce acute and enduring increases in reward responsiveness, partly through the 5-HT2A receptor, though the time course varies and clinical implications require further validation.

Δ 9 -Tetrahydrocannabinol-induced enhancement of reward responsivity via mesocorticolimbic modulation in squirrel monkeys.

bioRxiv : the preprint server for biology January 24, 2026 Kwang-Hyun Hur, Lisa D Nickerson, Jack Bergman et al.

THC, the psychoactive compound in cannabis, selectively amplifies behavioral and brain responses to cues that predict rewards, without affecting responses to neutral cues or baseline reward consumption. In squirrel monkeys, a low dose of THC (3 μg/kg) increased conditioned approach behavior toward a visual stimulus associated with food delivery. Functional MRI showed that THC enhanced activity in reward-related brain regions—anterior cingulate cortex, striatum, hippocampus, and substantia nigra-ventral tegmental area (SN-VTA)—while leaving visual and motor cortices unaffected. Resting-state connectivity analyses revealed that THC strengthened communication within mesocorticolimbic networks, with the SN-VTA acting as a central hub. These findings indicate that THC boosts incentive salience and motivational drive toward reward-associated stimuli through selective modulation of this circuitry.