Sun D.,120 Veterans Boulevard |
Ye Q.,Amgen |
Yan X.,120 Veterans Boulevard |
Rew Y.,120 Veterans Boulevard |
And 7 more authors.
ACS Medicinal Chemistry Letters | Year: 2014
In this letter, we reported the design and synthesis of three potent, selective, and orally bioavailable 11β-HSD1 inhibitors labeled with 14C: AMG 456 (1), AM-6949 (2), and AM-7715 (3). We evaluated the covalent protein binding of the labeled inhibitors in human liver microsomes in vitro and assessed their potential bioactivation risk in humans. We then studied the in vitro mechanism of 2 in human hepatocytes and the formation of reactive intermediates. Our study results suggest that 1 and 3 have low potential for metabolic bioactivation in humans, while 2 has relatively high risk. © 2014 American Chemical Society. Source
Dillon G.M.,Merck And Co. |
Lubbers L.S.,Neuroscience Drug Discovery |
Ferguson M.T.,Merck And Co. |
Lao J.Z.,Metabolic Disorders |
And 12 more authors.
Behavioural Pharmacology | Year: 2011
Cannabinoid receptors (CBRs) play an important role in a variety of physiological functions and have been considered drug targets for obesity and psychiatric disorders. In particular, the CB1R is highly expressed in brain regions crucial to learning and memory processes, and several lines of evidence indicate that pharmacological blockade of this receptor could have therapeutic applications in the treatment of cognitive disorders. In this study, we investigated whether MK-7128 (0.1, 0.3, and 1 mg/kg, orally), a novel and selective CB1R inverse agonist, could improve learning and memory deficits induced by scopolamine (1 mg/kg, subcutaneously) in mice. The investigators also assessed CB1R occupancy in the brain to ensure target engagement of MK-7128, and showed that MK-7128 significantly improved both Y-maze spontaneous alternation and object habituation performance in scopolamine-treated mice and inhibits the binding of radioiodinated AM251 in murine cortex and hippocampus. These data indicate that MK-7128 improves cognitive performance in a model of cholinergic hypofunction and suggest that efficacy is achieved at relatively low levels of CB1R occupancy in the brain. Our results extend earlier findings suggesting a role of CB1Rs in the modulation of memory processes and a potential therapeutic application for CB1R inverse agonists in cognitive disorders. © 2011 Wolters Kluwer Health | Lippincott Williams & Wilkins. Source
Researchers from the Duke-NUS Graduate Medical School Singapore (Duke-NUS) and Duke Medicine have identified a potential treatment strategy for an often-fatal inherited glycogen storage disease. E-published ahead of print recently in the Journal of Hepatology, the study provides much-needed hope for the management of glycogen storage disease Ia, known as GSDIa or von Gierke disease, a genetic metabolic disorder that requires lifelong dietary therapy. Patients with the disorder lack the enzyme that enables their livers to convert a glucose precursor to glucose during fasting conditions. Without release of glucose from the liver into the bloodstream, patients develop an extremely low blood sugar level that can lead to seizures, coma and death. To manage the condition, patients eat frequently and consume raw cornstarch on a strict schedule. But the inability of the liver to produce glucose results in an over-accumulation of glycogen and fat in the liver, which contributes to an enlarged and fatty liver. Eventually, many patients with GSDIa develop liver tumors and renal failure, and often die in early adulthood. “GSDIa is a devastating disease,” said senior author Paul Yen, M.D., of the Cardiovascular and Metabolic Disorders Programme at Duke-NUS. “Diet management is currently the only way to manage the disease, but it cannot prevent the more complex symptoms of the disorder related to organ failure.” Identifying the urgent need for alternative therapeutic strategies, Yen and colleagues collaborated with GSDIa expert Dwight Koeberl, M.D., Ph.D., a professor in the departments of Pediatrics and Molecular Genetics and Microbiology at Duke University School of Medicine. The international research team found that autophagy was impaired in animal liver cells modelled on GSDIa. Autophagy is a process in which a damaged cell degrades into its basic components and recycles itself for use by other cells. Impaired autophagy contributed to the pathology of GSDIa by disrupting fat metabolism that would otherwise aid the breakdown of fat stored in the liver. This disruption led to high fat levels, which would eventually cause fatty liver. With these findings, the team induced autophagy in cell and animal models and saw reductions in fat and glycogen levels. A drug commonly prescribed to prevent transplant rejection – rapamycin – stimulated autophagy and improved liver size and function in animal models. “By inducing autophagy, we are able to provide an alternate pathway for glycogen to be broken down into glucose,” said Benjamin Farah, first author of the study and a Duke-NUS M.D./Ph.D. student. “Activators of the autophagy pathway could be useful for treating GSDIa and other metabolic disease with fatty liver, without relying on the missing enzyme.” “I’ve been working with GSDIa patients throughout my career and have seen first-hand how difficult it is to manage,” Koeberl said. “At Duke, we’ve been working on gene therapies to target the missing enzyme, but I’m excited about the alternate treatment strategy that these findings offer. The possibility of using other approved drugs to develop therapeutic strategies to treat GSDIa gives us a more immediate solution.” The next step before the findings can be clinically applied is to conduct studies in animals using similar drugs, and determine the most effective drug therapy with the least side effects. The teams at Duke-NUS and Duke University plan to continue their collaboration to pursue this approach.
Kelly T.M.,Metabolic Disorders |
Kan Y.,Metabolic Disorders |
Palyha O.,Metabolic Disorders |
Guan X.-M.,Metabolic Disorders |
And 12 more authors.
ACS Medicinal Chemistry Letters | Year: 2012
Extensive structure-activity relationship studies of a series derived from atropisomer 1, a previously described chiral benzodiazepine sulfonamide series, led to a potent, brain penetrant and selective compound with excellent preclinical pharmacokinetic across species. We also describe the utilization of a high throughput mouse pharmacodynamic assay which allowed for expedient assessment of pharmacokinetic and brain distribution. © 2012 American Chemical Society. Source