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Loren Parsons' contribution to addiction neurobiology

机译:Loren Parsons对成瘾神经生物学的贡献

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Abstract Loren (Larry) H. Parsons passed away at the age of 51. In spite of his premature departure, Larry much contributed to the drug abuse field. Since his graduate studies for the Ph.D. in Chemistry in J.B. Justice lab, microdialysis is the tread that links Larry's research topics, namely, the role of dopamine (DA), serotonin (5‐HT), gamma‐aminobutyric acid (GABA), glutamate and endocannabinoids (eCBs) in drug reinforcement and dependence. Larry was the first to show that abstinence from chronic cocaine reduces extracellular DA in the NAc, consistent with the so called ‘dopamine depletion hypothesis’ of cocaine addiction. Another Larry's major contributions are the studies on 5‐HT and 5‐HT receptors' role in cocaine stimulant actions, which resulted in the identification of 5‐HT1B receptors as a critical substrate of cocaine reinforcement. By applying mass spectrometry to eCBs analysis in brain dialysates, Larry's lab showed that ethanol, heroin, nicotine and cocaine differentially affect anandamide and 2‐arachidonoylglicerol overflow in the NAc shell, a critical site of drugs of abuse DA stimulant actions. Larry also applied microdialysis to study GABA and glutamate's role in ethanol dependence and heroin reinforcement, providing in vivo evidence for a sensitization of corticotropin‐releasing factor‐dependent release of GABA in the central amygdala in withdrawal from chronic ethanol and for a reduction of GABA transmission in the ventral pallidum in heroin but not cocaine intravenous self‐administration. Larry showed the wide possibilities of microdialysis as a general purpose methodology for monitoring neurotransmitters and neuromodulators in the brain extracellular compartment. From this viewpoint, he stands as the best advocate for microdialysis.
机译:抽象Loren(Larry)H. Parsons在51岁时通过了。尽管他过早出发,Larry有助于滥用药物。自他的研究生以来为博士学位。在JB Justice Lab中的化学中,MicrodiaLysis是将Larry的研究主题联系起来的胎面,即多巴胺(DA),血清素(5-HT),γ-氨基丁酸(GABA),谷氨酸和内胆蛋白(ECBS)中的作用加强和依赖。拉里是第一个表明禁止慢性可卡因的禁欲减少了NAC的细胞外DA,与可卡因成瘾的所谓的“多巴胺耗尽假说”一致。另一个拉里的主要贡献是对可卡因兴奋剂作用中的5-HT和5-HT受体的作用的研究,这导致5-HT1B受体作为可卡因增强的关键基材。通过将质谱法施加到脑透析液中的ECBS分析中,Larry的实验室表明,乙醇,海洛因,尼古丁和可卡因差异地影响NAC壳中的Anandamide和2-arachidonlglicerol溢出,滥用DA兴奋剂药物的临界部位。 Larry还将Microdialysis应用于研究GABA和谷氨酸在乙醇依赖和海洛因增强中的作用,提供了体内证据,用于敏化Corticotropin释放因子依赖于慢性乙醇中的中央杏仁酵母中GABA的敏感性,并减少GABA传播在海洛因的腹侧苍白,但不可克里静脉的自我管理。 Larry显示了MicrodiaLysis的广泛可能性作为监测脑细胞外隔室中神经递质和神经调节剂的通用方法。从这个角度来看,他成为MicrodiaLysis的最佳倡导者。

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