Search for dark matter produced in association with bottom or top quarks in √s = 13 TeV pp collisions with the ATLAS detector

A search for weakly interacting massive particle dark matter produced in association with bottom or top quarks is presented. Final states containing third-generation quarks and miss- ing transverse momentum are considered. The analysis uses 36.1 fb−1 of proton–proton collision data recorded by the ATLAS experiment at √s = 13 TeV in 2015 and 2016. No significant excess of events above the estimated backgrounds is observed. The results are in- terpreted in the framework of simplified models of spin-0 dark-matter mediators. For colour- neutral spin-0 mediators produced in association with top quarks and decaying into a pair of dark-matter particles, mediator masses below 50 GeV are excluded assuming a dark-matter candidate mass of 1 GeV and unitary couplings. For scalar and pseudoscalar mediators produced in association with bottom quarks, the search sets limits on the production cross- section of 300 times the predicted rate for mediators with masses between 10 and 50 GeV and assuming a dark-matter mass of 1 GeV and unitary coupling. Constraints on colour- charged scalar simplified models are also presented. Assuming a dark-matter particle mass of 35 GeV, mediator particles with mass below 1.1 TeV are excluded for couplings yielding a dark-matter relic density consistent with measurements

Neurobiological basis of the nicotine withdrawal reaction : an experimental analysis

The mesolimbocortical dopamine (DA) system is pivotal for the mediation of the reinforcing effects of many dependence-producing drugs. It consists of cell bodies in the ventral tegmental area (VTA) that project to e.g. the nucleus accumbens (NAC), the central nucleus of amygdala (CNA) and the medial prefrontal cortex. In experimental animals, nicotine increases DA output in the NAC, exerts a locomotor stimulatory effect and is readily self-administered. These effects of systemic nicotine appear largely mediated via nicotinic receptors (nAChRs) in the VTA. Moreover, recently the a7 nAChR subtype has been implicated in some of the acute effects of nicotine. The effects of nicotine withdrawal on behavior and mesolimbocortical dopaminergic neurotransmission in rats have remained largely unknown. Therefore, utilizing behavioral methods, in vivo microdialysis, intracerebral drug injections and immunohistochemistry, we explored in detail the effects of nicotine withdrawal on these parameters. Rats were, by means of subcutaneously implanted minipumps, treated chronically with a dose of nicotine that yielded plasma levels similar to those encountered in heavy smokers. A somatic nicotine abstinence reaction was induced through removal of the infusion pump or through administration of a nAChR antagonist, acting either centrally and peripherally or peripherally only. Administration of nicotine or of a peripherally acting nAChR agonist both reversed the withdrawal reaction. Systemic administration of the nAChR antagonist mecamylamine significantly reduced DA output in the NAC selectively in the nicotine-treated group. The somatic withdrawal signs and the reduction in NAC DA appeared not to be specifically or causally related. Also intrategmental injection of mecamylamine elicited a reduction in accumbal DA output, somatic withdrawal signs as well as hypolocomotion, whereas intraaccumbal administration of mecamylamine failed to elicit any changes in NAC DA output or in somatic signs. Similarly, intrategmental application of an a7 nAChR antagonist resulted in a decreased NAC DA output and a reduction in locomotor activity. Finally, nicotine withdrawal precipitated by a systemic injection of mecamylamine both attenuated DA output and activated c?fos in the CNA. These results demonstrate a significant contribution of peripheral nAChRs to the nicotine withdrawal reaction and predict that drugs stimulating selectively peripheral nAChRs may have some usefulness in smoking cessation. The withdrawal-induced reduction in NAC DA, if it occurs also in man, may have bearing on clinical symptoms such as depression and dysphoria that are often encountered in association with smoking cessation. In addition, the clinical efficacy of bupropion in smoking cessation programmes may largely be due to its ability to restore a compromised mesolimbic DA function. Specifically, nAChRs at the level of the VTA rather than in the NAC seem to contribute to the behavioral and biochemical consequences of nicotine withdrawal precipitated with systemic mecamylamine, and a role for a7 nAChRs within the VTA is indicated in this regard. The withdrawal-induced selective activation of c-fos in the CNA may have bearing on anxiety and distress, symptoms that in animals can be elicited from this brain region and frequently occur in nicotine abstinent humans