TY - JOUR
T1 - The effects of delta-9-tetrahydrocannabinol exposure on female menstrual cyclicity and reproductive health in rhesus macaques
AU - Ryan, Kimberly S.
AU - Mahalingaiah, Shruthi
AU - Campbell, Lily R.
AU - Roberts, Victoria H.J.
AU - Terrobias, Juanito Jose D.
AU - Naito, Chelsey S.
AU - Boniface, Emily R.
AU - Borgelt, Laura M.
AU - Hedges, Jason C.
AU - Hanna, Carol B.
AU - Hennebold, Jon D.
AU - Lo, Jamie O.
N1 - Funding Information:
J.O.L. reports grants from the National Institutes of Health and March of Dimes for the submitted study. K.S.R. has nothing to disclose. S.M. has nothing to disclose. L.R.C. has nothing to disclose. V.H.J.R. has nothing to disclose. J.J.D.T. has nothing to disclose. C.S.N. has nothing to disclose. E.R.B. has nothing to disclose. L.M.B. has nothing to disclose. J.C.H. has nothing to disclose. C.B.H. has nothing to disclose. J.D.H. has nothing to disclose.
Funding Information:
The investigators thank the veterinary and husbandry staff that provided excellent care for the animals used in this study, in particular Dr. Lauren Drew Martin and Travis Hodge. Additionally, the investigators thank the Endocrine Technologies Core and Assisted Reproductive Core at the ONPRC as well as the Bioanalytical Shared Resource/Pharmacokinetics Core and Oregon Clinical and Translational Research Institute Laboratories at Oregon Health & Science University.
Funding Information:
For the financial support, all Oregon National Primate Research Center (ONPRC) cores and units were supported by the National Institutes of Health (NIH) Grant P51 OD011092. Research reported in this publication was supported by the Reproductive Scientist Development Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institute on Drug Abuse (NIDA), March of Dimes Foundation, and Silver Family Innovation Award under Award Numbers K12 HD000849 (to J.L.) and R03 HD097116 (to J.L.). The contents of this study are solely the responsibility of the investigators and do not necessarily represent the official view of NIH NICHD and NIDA.
Publisher Copyright:
© 2021 American Society for Reproductive Medicine
PY - 2021/8
Y1 - 2021/8
N2 - Objective: To determine the dose-dependent effect of contemporary marijuana exposure on female menstrual cyclicity and reproductive endocrine physiology in a nonhuman primate model. Design: Research animal study. Setting: Research institute environment. Animals: Adult female rhesus macaques (6–12 years of age; n = 8). Intervention(s): Daily delta-9-tetrahydrocannabinol (THC) edible at medically and recreationally relevant contemporary doses. Main Outcome Measure(s): Menstrual cycle length (MCL), anti-Müllerian hormone, prolactin, basal follicle-stimulating hormone (FSH), estradiol (E2) and progesterone, luteinizing hormone (LH), and thyroid-stimulating hormone. Result(s): The average before THC weight was 6.9 kg (standard deviation, 0.8), and at the highest THC dosing, the average weight was 7.2 kg (standard deviation, 0.8). With increasing THC dosing, MCL and FSH concentrations increased, while basal E2 concentration was stable. The average MCL concentration increased 4.0 days for each mg/7 kg/day of THC (95% CI, 1.4–6.6 days). Follicle-stimulating hormone concentration increased significantly with increasing THC dose, 0.34 ng/mL for each mg/7 kg/day of THC (95% CI, 0.14–0.57 ng/mL). No significant trends were observed between THC dosing and average basal progesterone, anti-Müllerian hormone, prolactin, LH, or thyroid-stimulating hormone concentrations. Conclusion(s): In rhesus macaques, a dose response toward increased MCL and basal FSH concentrations but plateau of basal E2 and LH concentrations was observed with increasing THC dosing, suggesting ovulatory dysfunction. Further studies are needed to determine the effects of a longer duration of exposure and whether the significant increase in MCL and FSH concentrations results in reduced fecundity.
AB - Objective: To determine the dose-dependent effect of contemporary marijuana exposure on female menstrual cyclicity and reproductive endocrine physiology in a nonhuman primate model. Design: Research animal study. Setting: Research institute environment. Animals: Adult female rhesus macaques (6–12 years of age; n = 8). Intervention(s): Daily delta-9-tetrahydrocannabinol (THC) edible at medically and recreationally relevant contemporary doses. Main Outcome Measure(s): Menstrual cycle length (MCL), anti-Müllerian hormone, prolactin, basal follicle-stimulating hormone (FSH), estradiol (E2) and progesterone, luteinizing hormone (LH), and thyroid-stimulating hormone. Result(s): The average before THC weight was 6.9 kg (standard deviation, 0.8), and at the highest THC dosing, the average weight was 7.2 kg (standard deviation, 0.8). With increasing THC dosing, MCL and FSH concentrations increased, while basal E2 concentration was stable. The average MCL concentration increased 4.0 days for each mg/7 kg/day of THC (95% CI, 1.4–6.6 days). Follicle-stimulating hormone concentration increased significantly with increasing THC dose, 0.34 ng/mL for each mg/7 kg/day of THC (95% CI, 0.14–0.57 ng/mL). No significant trends were observed between THC dosing and average basal progesterone, anti-Müllerian hormone, prolactin, LH, or thyroid-stimulating hormone concentrations. Conclusion(s): In rhesus macaques, a dose response toward increased MCL and basal FSH concentrations but plateau of basal E2 and LH concentrations was observed with increasing THC dosing, suggesting ovulatory dysfunction. Further studies are needed to determine the effects of a longer duration of exposure and whether the significant increase in MCL and FSH concentrations results in reduced fecundity.
KW - Cannabis
KW - female reproductive health
KW - marijuana
KW - menstrual cycle
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U2 - 10.1016/j.xfss.2021.05.001
DO - 10.1016/j.xfss.2021.05.001
M3 - Article
C2 - 34901892
AN - SCOPUS:85122742515
SN - 2666-335X
VL - 2
SP - 287
EP - 294
JO - F and S Science
JF - F and S Science
IS - 3
ER -