PMID- 37358825 OWN - NLM STAT- MEDLINE DCOM- 20230908 LR - 20230911 IS - 1745-1701 (Electronic) IS - 0586-7614 (Print) IS - 0586-7614 (Linking) VI - 49 IP - 5 DP - 2023 Sep 7 TI - Social Psychopharmacology: Novel Approaches to Treat Deficits in Social Motivation in Schizophrenia. PG - 1161-1173 LID - 10.1093/schbul/sbad094 [doi] AB - BACKGROUND AND HYPOTHESIS: Diminished social motivation is a negative symptom of schizophrenia and leads to severe functional consequences for many patients suffering from the illness. However, there are no effective medications available to treat this symptom. Despite the lack of approved treatments for patients, there is a growing body of literature on the effects of several classes of drugs on social motivation in healthy volunteers that may be relevant to patients. The aim of this review is to synthesize these results in an effort to identify novel directions for the development of medications to treat reduced social motivation in schizophrenia. STUDY DESIGN: In this article, we review pharmacologic challenge studies addressing the acute effects of psychoactive drugs on social motivation in healthy volunteers and consider how these findings may be applied to deficits in social motivation in schizophrenia. We include studies testing amphetamines and 3,4-methylenedioxymethamphetamine (MDMA), opioids, cannabis, serotonergic psychedelics, antidepressants, benzodiazepines, and neuropeptides. STUDY RESULTS: We report that amphetamines, MDMA, and some opioid medications enhance social motivation in healthy adults and may represent promising avenues of investigation in schizophrenia. CONCLUSIONS: Given the acute effects of these drugs on behavioral and performance-based measures of social motivation in healthy volunteers, they may be particularly beneficial as an adjunct to psychosocial training programs in patient populations. It remains to be determined how these medications affect patients with deficits in social motivation, and in which contexts they may be most effectively administered. CI - Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center 2023. FAU - Bershad, Anya K AU - Bershad AK AUID- ORCID: 0000-0002-3011-3730 AD - Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles Semel Institute for Neuroscience and Human Behavior, Los Angeles, CAUSA. FAU - de Wit, Harriet AU - de Wit H AUID- ORCID: 0000-0002-7211-8994 AD - Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, ILUSA. LA - eng GR - R01 DA002812/DA/NIDA NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Review PL - United States TA - Schizophr Bull JT - Schizophrenia bulletin JID - 0236760 RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) SB - IM MH - Adult MH - Humans MH - *Schizophrenia MH - Motivation MH - *Psychopharmacology MH - *N-Methyl-3,4-methylenedioxyamphetamine/therapeutic use MH - *Apathy PMC - PMC10483474 OTO - NOTNLM OT - Amotivation OT - approach and avoidance OT - human behavioral pharmacology COIS- HdW is on the Board of Directors of PharmAla Biotech and consultant to Awakn Life Sciences and Gilgamesh Pharmaceuticals. These are unrelated to this manuscript. EDAT- 2023/06/26 13:07 MHDA- 2023/09/08 06:43 PMCR- 2024/06/26 CRDT- 2023/06/26 11:22 PHST- 2024/06/26 00:00 [pmc-release] PHST- 2023/09/08 06:43 [medline] PHST- 2023/06/26 13:07 [pubmed] PHST- 2023/06/26 11:22 [entrez] AID - 7207745 [pii] AID - sbad094 [pii] AID - 10.1093/schbul/sbad094 [doi] PST - ppublish SO - Schizophr Bull. 2023 Sep 7;49(5):1161-1173. doi: 10.1093/schbul/sbad094.