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Translational Research Institute

UAMS Synthetic ‘Marijuana’ Researcher Presents Findings at National Meeting

Anna Radominska-Pandya, Ph.D., (left front) with UAMS synthetic “marijuana” research team members, including Laura James, M.D., (right), and (back, l-r) Principal Investigator Paul Prather, Ph.D., Jeff Moran, Ph.D., and William Fantegrossi, Ph.D.

LITTLE ROCK — Some people who use so-called synthetic marijuana, known by names such as K2 and Spice, may be unable to metabolize the drug, leading them to experience its most harmful effects, a UAMS researcher said at the recent national Experimental Biology 2017 meeting in Chicago.

Anna Radominska-Pandya, Ph.D., part of a UAMS research team examining how the body processes the man-made cannabinoids, presented the team’s findings on the harmful effects of synthetic marijuana at the American Society for Pharmacology and Experimental Therapeutics annual meeting, which was held during Experimental Biology, a meeting that draws thousands.

Synthetic “marijuana” is a growing group of man-made cannabinoids marketed as alternatives to marijuana. Although the man-made drugs activate the same receptors in the brain as natural marijuana, they are known to have volatile effects that can lead to severe injury and death.

Radominska-Pandya is a professor in the UAMS College of Medicine Departments of Biochemistry and Molecular Biology and Medicine. Her work could identify genetic risk factors that make some people susceptible to the synthetic cannabinoids’ most harmful consequences, potentially leading to antidotes that counteract the worst effects.

Radominska-Pandya and her colleagues have found that some people are unable to metabolize and excrete synthetic cannabinoids. They now hypothesize that a person’s genetic makeup could produce the metabolism defects that cause the most harmful effects from the drug. Future genetics tests could potentially identify those people.

“It is important to understand the underlying causes and toxicity of synthetic cannabinoids so that effective treatments and antidotes can be developed,” Radominska-Pandya said.

UAMS has been a national leader of synthetic cannabinoid research since the UAMS Translational Research Institute funded the team’s work in 2011 with a $100,000 pilot award. In 2016, the team, led by Paul Prather, Ph.D., a professor in the Department of Pharmacology and Toxicology, received a five-year, $2.7 million National Institute of Drug Abuse grant that builds on the work of the pilot study.

Synthetic cannabinoids come in more than 150 chemical forms and the list is growing. As new synthetic cannabinoids appear on the market, the UAMS research team will study their properties and how the body’s metabolism may contribute to their harmful effects.

Experimental Biology is an annual meeting comprised of more than 14,000 scientists and exhibitors from six host societies and multiple guest societies. With a mission to share the newest scientific concepts and research findings shaping clinical advances, the meeting offers an unparalleled opportunity for exchange among scientists from across the United States and the world who represent dozens of scientific areas, from laboratory to translational to clinical research.

Filed Under: Front, News Tagged With: Anna Radominska-Pandya, Experimental Biology, genetics, k2, spice, synthetic marijuana, Translational Research Institute, UAMS

TRI Part of NIH Milestone to Accelerate Multisite Clinical Studies

CTSA Program paves way for nationwide single IRB model.

Developing new treatments for diseases often requires large numbers of clinical research participants enrolled in the same study at numerous geographical sites. These multisite clinical trials are well-positioned to discover whether a promising therapeutic is safe and effective, and may provide medical professionals with the information needed for treating their patients. However, the initiation of such studies may be delayed because each site typically relies on its own Institutional Review Boards (IRBs) to provide ethics reviews of the risks and benefits of the proposed research.

Christopher P. Austin, M.D.

The National Institutes of Health (NIH) is leading policy and programmatic initiatives to streamline this overly cumbersome process. NIH’s National Center for Advancing Translational Sciences (NCATS) announced today that all Clinical and Translational Science Awards (CTSA) Program sites (including the UAMS Translational Research Institute) have signed on to the NCATS Streamlined, Multisite, Accelerated Resources for Trials (SMART) IRB authorization agreement. This agreement — which now includes a total of more than 150 top medical research institutions — will enable all participating study sites to rely on the ethics review of one IRB for each study, making it possible to initiate multisite studies within weeks instead of months. For patients waiting to enroll in a study, this could make a life-saving difference.

The SMART IRB authorization agreement serves as a model to help investigators adhere to the NIH’s policy on single IRB use for multisite studies. This policy was designed to improve IRB efficiencies while ensuring the protection of research participants so that research can proceed expeditiously.

The authorization agreement effort was led by Harvard Catalyst, University of Wisconsin-Madison Institute for Clinical and Translational Research, and Dartmouth Synergy. Through these institutions, a team of NCATS-supported SMART IRB ambassadors facilitated and provided critical guidance and support to assist institutions in joining and implementing the SMART IRB authorization agreement.

“This milestone is a giant step toward a nationwide model for greater efficiency in IRB review, which is critical to getting more treatments to more patients more quickly,” said NCATS Director Christopher P. Austin, M.D. “It was made possible by the teamwork of hundreds of experts across the country who worked together to achieve what was thought to be impossible even a few years ago.”

In addition, the SMART IRB authorization agreement will provide the foundation for NCATS’ Trial Innovation Network central IRBs. The Trial Innovation Network is a collaborative CTSA Program initiative designed to address critical roadblocks in clinical research, and to optimize and streamline the clinical trial and studies process.

Next steps for the NCATS SMART IRB Platform include the development of education, training and harmonization of best practices for a single IRB review. Learn more at https://ncats.nih.gov/expertise/clinical/smartirb and https://smartirb.org (link is external).

About the National Center for Advancing Translational Sciences (NCATS): To get more treatments to more patients more quickly, NCATS incorporates the power of data, new technologies and strategic collaborations to develop, demonstrate and disseminate innovations in translational science. Rather than targeting a particular disease or fundamental science, NCATS focuses on what is common across all diseases and the translational process. Learn more at https://ncats.nih.gov.

About the National Institutes of Health (NIH): NIH, the nation’s medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit www.nih.gov.

Filed Under: Front, News, Newsroom Tagged With: Christopher P. Austin, CTSA, IRB, NCATS, NIH, SMART IRB, Translational Research Institute, UAMS

TRI Seeks Early-Career Researchers Interested in Becoming Grant Reviewers

TRI is looking for early-career investigators at UAMS/ACRI/CAVHS who are interested in participating in mentored grant reviews.

This learning opportunity will include mentored reviews of TRI-sponsored pilot awards and KL2 Scholar awards along with independent training utilizing NIH resources.

If you are interested, please submit this brief form. After collecting names through the end of the year, TRI will contact registrants about next steps.  

Filed Under: Front, News, Newsroom Tagged With: early career, grant reviewer, researchers, Translational Research Institute, UAMS

‘Dos & Don’ts of Community Engagement’ Workshop for Researchers

A new workshop on the Dos and Don’ts of Community Engagement is being offered to researchers, students and staff, Oct. 18, 1 – 5 p.m., College of Public Health, G232.

The workshop was developed by the Translational Research Institute, College of Public Health and UAMS’ community partners. The workshop will include simulation and role reversal, video testimonials, and group reflection and debriefing.  The objective is to increase researchers’ knowledge of the dos and don’ts of community engaged research in the research domains of entering the community; the realities and constraints of community-based organizations; and dissemination.

The workshop is supported by the Arkansas Prevention Research Center and the Arkansas Center for Health Disparities.

For more information, contact jcoffey@uams.edu.

Filed Under: Front, News, Newsroom Tagged With: Community Engagement, Dos and Don'ts, research, Translational Research Institute, TRI, UAMS, University of Arkansas for Medical Sciences

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