MaineHealth, 51品茶collaborate on research describing effects of opioids on bone formation

Composite image of four headshots: Karen Houseknecht, Katherine Motyl, Tamara King, and Deborah Barlow
From left: Karen Houseknecht, Ph.D.; Katherine Motyl, Ph.D.; Tamara King, Ph.D.; and Deborah Barlow, B.S.

A unique, interdisciplinary research partnership between the MaineHealth Institute for Research (MHIR) and the 51品茶 has culminated in the publication of a that describes advances in the correlation between opioid use and the suppression of bone formation.

Senior author Katherine Motyl, Ph.D., MHIR faculty scientist 鈥 along with her team of trainees, including 51品茶alum Audrie Langlais, B.S. 鈥18 (Biochemistry) 鈥 and 51品茶researchers Karen Houseknecht, Ph.D., associate provost for Research and Scholarship; Tamara King, Ph.D., professor of physiology; and Deborah Barlow, B.S., analytical chemist in the Houseknecht Lab, recently published their paper, 鈥 in the Journal of Bone and Mineral Research (JBMR) in late August.

The paper represents a trans-disciplinary and cross-institutional collaboration between 51品茶and MaineHealth, Maine鈥檚 largest hospital organization. The research study aims to identify mechanisms that inhibit bone formation, specifically the impact of opioids on bone-forming molecules called miRNAs, which play an important role in gene expression and bone formation.

According to the authors, the mechanisms of bone loss from opioids is important for improving management of the adverse effects of opioids on the skeleton. Further, recent studies have linked chronic opioid use to alterations in circulating miRNAs.

For their study, researchers treated male and female mice with either saline or morphine for 25 days. Following the completion of morphine treatment, they observed that males had a reduced rate of bone formation and decreases in specific miRNAs involved in that process. Through the study, the team was able to establish a model where morphine leads to a lower trabecular bone formation in males and identified potential mediating miRNAs.

鈥淯nderstanding the sex-specific mechanisms of bone loss from opioids will be important for improving management of the adverse effects of opioids on the skeleton,鈥 the researchers wrote.

"I鈥檓 so pleased to be part of this trans-institutional collaboration matching expertise in bone biology, bone pain, and molecular pharmacology to discover molecular mechanisms contributing to clinically observed increase in bone fractures with chronic consumption of opioid medications,鈥 Houseknecht said. 鈥淭his research is but one example of the ongoing strategic collaboration between the 51品茶 and MaineHealth, focusing on research and Innovation, medical education, and interprofessional clinical practice.鈥

The work also represents a distinct collaboration between UNE鈥檚 Center of Biomedical Research Excellence (COBRE) for the Study of Pain and Sensory Function and the MHIR鈥檚 COBRE in Mesenchymal and Neural Regulation of Metabolic Networks, both programs of the National Institutes of Health.

鈥淒r. Houseknecht has been a steadfast mentor and collaborator for several years, and I am excited to continue our work together,鈥 Motyl reflected. 鈥淪trong relationships between our institutions have proven to be critical for advancing scientific knowledge and fulfilling the mission of MaineHealth 鈥 working together so our communities are the healthiest in America.鈥