The SEX-specific role of sumoylation in heroin seeking

Active Project Grant Awarded Last action

Award ID
R21DA062756
Recipient
Awarding agency
Obligated
$377,586

Award facts

Assistance listing
93.279 Drug Use and Addiction Research Programs
Completion date 38% complete
Place of performance
Tulsa, OK 74107, USA

Award details come from USAspending.gov.

About this award

The National Institute on Drug Abuse awarded Oklahoma State University's Center for Health Sciences $377,586 on February 15, 2026, under the Drug Use and Addiction Research Programs (CFDA 93.279) to investigate sex-specific mechanisms of sumoylation in heroin-seeking behavior and neuroadaptation.

The research examines how sumoylation, a post-translational protein modification mediated by the enzyme UBC9, influences heroin seeking differently in males and females and affects target proteins underlying heroin-induced neurobiological changes. The work addresses a gap in understanding long-term neuroadaptations contributing to opioid use disorder, which remains a public health emergency with limited therapeutic options. Preliminary findings show sex-specific patterns in sumoylated proteins in the nucleus accumbens following heroin self-administration, with females demonstrating higher drug-taking behavior than males and altered UBC9 levels following ovarian hormone depletion.

The award funds basic research conducted in Tulsa, Oklahoma, with a performance period extending from February 15, 2026, through January 31, 2028. Virginia Polytechnic Institute & State University serves as a sub-recipient through Dr. Timothy Jarome, who functions as co-principal investigator and subcontractor. Dr. Jarome is responsible for tissue processing and analysis of tandem ubiquitin binding entity liquid chromatography–mass spectrometry (TUBE-LC/MS) data, provision of CRISPR plasmid materials to the principal investigator's laboratory, data interpretation, and collaboration on manuscript writing and presentation.

Description

Abstract
The goal of this proposal is to understand how SEX-specific sumoylation, a post-translational modification mediated by the enzyme UBC9, influences heroin seeking and the functionality of target proteins underlying heroin-induced neuroadaptations. Heroin use disorder has risen to a public health emergency with limited therapeutic options that do not provide permanent symptom alleviation. Limited understanding of long-term neuroadaptations has stymied the development of successful therapeutics. Moreover, despite females being more susceptible to opioid craving and relapse when compared to males, the mechanisms mediating this SEX- dependent predisposition remain equivocal. Our group has recently shown SEX-specific patterns in sumoylation underlying fear memory processing. However, the role of SEX-specific sumoylation in influencing brain mechanisms by drugs of abuse, including opioids, remains unknown. In our preliminary studies, we identified 9 sumoylated proteins in the nucleus accumbens of males at early abstinence following heroin self-administration, but no significantly altered proteins were identified in females. Parallelly, we found that females self-administered a significantly higher number of heroin infusions than males in self-administration behavior, and CUE-induced heroin-seeking is potentiated in both males and females at prolonged abstinence (abstinence day 14) when compared to early abstinence, which led US to hypothesize that temporal neuroadaptations contribute to persistent behavioral expression. We also found that depleting ovarian hormones through ovariectomy resulted in significantly higher drug-taking behavior and reduction in UBC9 levels in ovariectomized females when compared to the sham heroin counterpart. Based on these results, we propose to examine the SEX-specific mechanisms through which sumoylation dictates heroin-induced behavioral and neurobiological changes. In aim 1, we will utilize a novel sumo-specific proteomic analysis to identify SEX-specific sumoylated targets at prolonged abstinence. We will then examine how the viral mediated expression of sumo deficient TCP-1Η in the NAC shell changes its functionality. In aim 2, we will use crispr-mediated bidirectional regulation of UBC9 coding gene UBE2I and viral-mediated expression of wild-type and sumo deficient TCP-1Η to test if sumoylation is critical for active heroin taking and CUE-induced heroin-seeking behavior and if this modulation diverges based on SEX and abstinence. Collectively, this study will answer for the first time a comprehensive understanding of the role of SEX-specific sumoylation in influencing heroin-induced behavioral and neurobiological changes during abstinence. Such knowledge will hold clinical relevance in designing the next generation of therapeutics.

Subawards

Subrecipient Amount Awarded
Virginia Polytechnic Institute & State University Dr. Timothy Jarome will serve as a subcontractor and co-principal investigator on this R21 proposal. Dr. Jarome will be responsible for tissue processing and… $172,220

Quick answers

Who received award R21DA062756?

R21DA062756 was awarded to Oklahoma State University by National Institute on Drug Abuse (National Institutes of Health) on February 15, 2026.

How much is award R21DA062756 worth?

$377,586 has been obligated on R21DA062756.

On GovTribe

See this award's full record

  • Every transaction and subaward
  • The recipient's other awards and teaming partners
  • Similar grant awards
  • Ask GovTribe AI about this award