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Hainline, J.

Publications and source records attributed to Hainline, J..

2 recordsLinked to original sources

Acetaminophen attenuates pathological pain through a mechanism that requires CB1 cannabinoid receptors and the enzyme diacylglycerol lipase in mice

Acetaminophen (APAP) produces analgesia through mechanisms that remain poorly understood. Here, we tested the hypothesis that APAP-induced suppression of pathological pain is associated with cannabinoid receptors and activity of enzymes regulating endogenous lipids (diacylglycerol lipase, DAGL; monoacylglycerol lipase, MAGL) including endocannabinoids. APAP suppressed mechanical hypersensitivity in mouse models of post-surgical and inflammatory pain and the DAGL inhibitors (RHC-80267, DO34) and MAGL inhibitor JZL184 blocked APAPs analgesic effects. Global (rimonabant, AM251) but not peripherally restricted (AM6545) cannabinoid receptor antagonists prevented APAP-induced analgesia. APAP increased corticosterone levels >2-fold and reduced prostaglandins >5-fold across the brain and in the paw skin. In addition, APAP reduced up to 39% of signaling lipids detected in the targeted screen in CFA-treated subjects in a tissue-dependent manner. These observations suggest that APAP plays a wider role in endogenous lipid signaling than previously hypothesized and provides novel insight into mechanisms of action.

neuroscience↗

Deep learning and cross-species analysis identify the influences of sex and cannabinoidsignaling on cerebellar vermis morphology

The cerebellum is the only folded cortical structure present in both rodents and humans, allowing mechanistic studies of gyrification across species. In mice, the extent of anterior vermis folding and the shapes of white matter exhibit sex-dependent differences. We trained a deep convolutional neural network to predict biological sex from midline cerebellar MRI images, showing that human cerebellar midvermis contains sex-dependent anatomical features. Our comparative cross-species analysis shows that in both species, sex and anterior vermis folding patterns are not enough to predict an individuals behavior because the variability in performance between individuals is far greater than the differences between conditions. Finally, utilizing constitutive cannabinoid receptor 1 (CB1) knockout (KO) mice, we identify developmental cannabinoid signaling as a novel molecular mechanism limiting secondary fissure formation. TeaserMales and females display differences in the architecture of cerebellar folding shaped by cannabinoid signaling during development.

neuroscience↗