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pro vyhledávání: '"B. F. Cravatt"'
Autor:
J L, Wilkerson, S, Ghosh, D, Bagdas, B L, Mason, M S, Crowe, K L, Hsu, L E, Wise, S G, Kinsey, M I, Damaj, B F, Cravatt, A H, Lichtman
Publikováno v:
British journal of pharmacology. 173(10)
Inhibition of diacylglycerol lipase (DGL)β prevents LPS-induced pro-inflammatory responses in mouse peritoneal macrophages. Thus, the present study tested whether DGLβ inhibition reverses allodynic responses of mice in the LPS model of inflammatory
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Publikováno v:
British journal of pharmacology. 164(6)
Depolarization-induced suppression of inhibition (DSI) and excitation (DSE) are two forms of cannabinoid CB(1) receptor-mediated inhibition of synaptic transmission, whose durations are regulated by endocannabinoid (eCB) degradation. We have recently
Autor:
K. Monory, B. F. Cravatt, Shahnaz Christina Azad, G. Marsicano, W. Zieglgänsberger, G. Rammes, B. Lutz
Publikováno v:
AINS - Anästhesiologie · Intensivmedizin · Notfallmedizin · Schmerztherapie. 40
Autor:
M P, Patricelli, B F, Cravatt
Publikováno v:
Vitamins and hormones. 62
Fatty acid amides (FAAs) represent a growing family of biologically active lipids implicated in a diverse range of cellular and physiological processes. At present, two general types of fatty acid amides, the N-acylethanolamines (NAEs) and the fatty
Publikováno v:
Current pharmaceutical design. 4(4)
Oleamide is an endogenous fatty acid primary amide that accumulates in the cerebrospinal fluid under conditions of sleep deprivation and induces physiological sleep in animals. A review covering its discovery, its implications, and the emerging biolo
Publikováno v:
Journal of neuroscience research. 50(6)
Fatty acid amide hydrolase (FAAH) is a membrane-bound enzyme activity that degrades neuromodulatory fatty acid amides, including oleamide and anandamide. A single 2.5-kb FAAH mRNA is distributed throughout the rat CNS and accumulates progressively be