Δ9-tetrahydrocannabinol(THC)of cannabis is the main psychoactive component which is a global significant concern to human health.Evaluation on THC reported its drastic effect on the brain dopaminergic(DAergic)system ...Δ9-tetrahydrocannabinol(THC)of cannabis is the main psychoactive component which is a global significant concern to human health.Evaluation on THC reported its drastic effect on the brain dopaminergic(DAergic)system stimulating mesolimbic DA containing neurons thereby increasing the level of striatal DA.Cannabidiol(CBD),with its anxiolytic and anti-psychotic property,is potent to ameliorate the THC-induced DAergic variations.Legal authorization of cannabis use and its analogs in most countries led to a drastic dispute in the elicitation of cannabis products.With a recent increase in cannabis-induced disorder rates,the present review highlighted the detrimental effects of THC and the effects of CBD on THC induced alterations in DA synthesis and release.Alongside the reported data,uses of cannabis as a therapeutic medium in a number of health complications are also being briefly reviewed.These evaluated reports led to an anticipation of additional research contradictory to the findings of THC and CBD activity in the brain DAergic system and their medical implementations as therapeutics.展开更多
Cannabinoids are lipophilic substances derived from Cannabis sativa that can exert a variety of effects in the human body.They have been studied in cellular and animal models as well as in human clinical trials for th...Cannabinoids are lipophilic substances derived from Cannabis sativa that can exert a variety of effects in the human body.They have been studied in cellular and animal models as well as in human clinical trials for their therapeutic benefits in several human diseases.Some of these include central nervous system(CNS)diseases and dysfunctions such as forms of epilepsy,multiple sclerosis,Parkinson’s disease,pain and neuropsychiatric disorders.In addition,the endogenously produced cannabinoid lipids,endocannabinoids,are critical for normal CNS function,and if controlled or modified,may represent an additional therapeutic avenue for CNS diseases.This review discusses in vitro cellular,ex vivo tissue and in vivo animal model studies on cannabinoids and their utility as therapeutics in multiple CNS pathologies.In addition,the review provides an overview on the use of cannabinoids in human clinical trials for a variety of CNS diseases.Cannabinoids and endocannabinoids hold promise for use as disease modifiers and therapeutic agents for the prevention or treatment of neurodegenerative diseases and neurological disorders.展开更多
The renewed interest in dimeric salicylates as broad-spectrum anti-inflammatory and antidiabetic agents provided a rationale to investigate the dimerization of the substituted salicylate D9-tetrahydrocannabinolic acid...The renewed interest in dimeric salicylates as broad-spectrum anti-inflammatory and antidiabetic agents provided a rationale to investigate the dimerization of the substituted salicylate D9-tetrahydrocannabinolic acid(THCA-A, 3 a) as a strategy to solve its instability to decarboxylation and to generate analogues and/or pro-drugs of this native pre-cannabinoid. Activation of the carboxylic group with the DCC-HOBt-DMAP protocol afforded a high yield of the OBt ester 4, that was next converted into the highly crystalline di-depsidic dimer 5 upon treatment with DMAP. The mono-depsidic dimer 6 was also formed when the reaction was carried out with partially decarboxylated THCA-A samples. The structure of the depsidic dimers was established by spectroscopic methods and by aminolysis of 5 into the pre-cannabinoid amide 7. Both dimers showed excellent shelf stability and did not generate significant amounts of D9-THC upon heating. However, only the didepsidic dimer 5 activated PPAR-g, the major target of pre-cannabinoids, but strong binding to serum proteins abolished this activity, also shielding it from the action of esterases.展开更多
Plants synthesize an astonishing diversity of isoprenoids,some of which play essential roles in photosynthesis,respiration,and the regulation of growth and development.Two independent pathways for the biosynthesis of ...Plants synthesize an astonishing diversity of isoprenoids,some of which play essential roles in photosynthesis,respiration,and the regulation of growth and development.Two independent pathways for the biosynthesis of isoprenoid precursors coexist within the plant cell: the cytosolic mevalonic acid (MVA) pathway and the plastidial methylerythritol phosphate (MEP) pathway.However,little is known about the effects of plant hormones on the regulation of these pathways.In the present study we investigated the effect of gibberellic acid (GA3) on changes in the amounts of many produced terpenoids and the activity of the key enzymes,1-deoxy-D-xylulose 5-phosphate synthase (DXS) and 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR),in these pathways.Our results showed GA3 caused a decrease in DXS activity in both sexes that it was accompanied by a decrease in chlorophylls,carotenoids and 9-tetrahydrocannabinol (THC) contents and an increase in α-tocopherol content.The treated plants with GA3 showed an increase in HMGR activity.This increase in HMGR activity was followed by accumulation of stigmasterol and β-sitosterol in male and female plants and campestrol in male plants.The pattern of the changes in the amounts of sterols was exactly similar to the changes in the HMGR activity.These data suggest that GA3 can probably influence the MEP and MVA pathways oppositely,with stimulatory and inhibitory effects on the produced primary terpenoids in MVA and DXS pathways,respectively.展开更多
目的：建立气相色谱-质谱法同时分析运动营养品中大麻酚、大麻二酚和Δ9-四氢大麻酚的检测方法。方法：样品采用液液萃取,提取液经过正相固相萃取柱（Silica）纯化,洗脱液氮气吹干,N-甲基-N-（三甲基硅烷）三氟乙酰胺衍生化后,采用HP-1M...目的：建立气相色谱-质谱法同时分析运动营养品中大麻酚、大麻二酚和Δ9-四氢大麻酚的检测方法。方法：样品采用液液萃取,提取液经过正相固相萃取柱（Silica）纯化,洗脱液氮气吹干,N-甲基-N-（三甲基硅烷）三氟乙酰胺衍生化后,采用HP-1MS柱（17 m×0.2 mm i.d.×0.11 mm）色谱分离,程序升温,质谱检测,D3-Δ9-四氢大麻酚为内标。结果：大麻酚、大麻二酚和Δ9-四氢大麻酚的衍生化产物实现基线分离,三个定性特征离子的峰度比计算结果可以满足世界反兴奋剂机构（WADA）要求。该方法的检测限为1μg/kg,定量限为2μg/kg,在添加的高、中、低三种浓度的相对回收率分布在94%~119%之间。结论：该方法满足常规检测要求,样品前处理简单、快速、可靠。展开更多
基金The authors sincerely acknowledge the funding(Sanction Order No.DST/Inspire Fellowship/2016/IF160620)dated 01-22-2020 and support provided by the Department of Science and Technology,Govt.of India and University Grants Commission,New Delhi.
文摘Δ9-tetrahydrocannabinol(THC)of cannabis is the main psychoactive component which is a global significant concern to human health.Evaluation on THC reported its drastic effect on the brain dopaminergic(DAergic)system stimulating mesolimbic DA containing neurons thereby increasing the level of striatal DA.Cannabidiol(CBD),with its anxiolytic and anti-psychotic property,is potent to ameliorate the THC-induced DAergic variations.Legal authorization of cannabis use and its analogs in most countries led to a drastic dispute in the elicitation of cannabis products.With a recent increase in cannabis-induced disorder rates,the present review highlighted the detrimental effects of THC and the effects of CBD on THC induced alterations in DA synthesis and release.Alongside the reported data,uses of cannabis as a therapeutic medium in a number of health complications are also being briefly reviewed.These evaluated reports led to an anticipation of additional research contradictory to the findings of THC and CBD activity in the brain DAergic system and their medical implementations as therapeutics.
基金supported in part by grants from the National Institute on Aging and National Eye Institute[EY030747(3R01EY030747-02S2)and EY031248(3R01EY03124802S1)]of the National Institutes of Health(to PK)Additional support by the Felix and Carmen Sabates Missouri Endowed Chair in Vision Researchthe Vision Research Foundation of Kansas City。
文摘Cannabinoids are lipophilic substances derived from Cannabis sativa that can exert a variety of effects in the human body.They have been studied in cellular and animal models as well as in human clinical trials for their therapeutic benefits in several human diseases.Some of these include central nervous system(CNS)diseases and dysfunctions such as forms of epilepsy,multiple sclerosis,Parkinson’s disease,pain and neuropsychiatric disorders.In addition,the endogenously produced cannabinoid lipids,endocannabinoids,are critical for normal CNS function,and if controlled or modified,may represent an additional therapeutic avenue for CNS diseases.This review discusses in vitro cellular,ex vivo tissue and in vivo animal model studies on cannabinoids and their utility as therapeutics in multiple CNS pathologies.In addition,the review provides an overview on the use of cannabinoids in human clinical trials for a variety of CNS diseases.Cannabinoids and endocannabinoids hold promise for use as disease modifiers and therapeutic agents for the prevention or treatment of neurodegenerative diseases and neurological disorders.
基金financial support to the groups in Novara and Naples(PRIN2017,Project 2017WN73PL,bioactivity-directed exploration of thephytocannabinoid chemical space,Italy)
文摘The renewed interest in dimeric salicylates as broad-spectrum anti-inflammatory and antidiabetic agents provided a rationale to investigate the dimerization of the substituted salicylate D9-tetrahydrocannabinolic acid(THCA-A, 3 a) as a strategy to solve its instability to decarboxylation and to generate analogues and/or pro-drugs of this native pre-cannabinoid. Activation of the carboxylic group with the DCC-HOBt-DMAP protocol afforded a high yield of the OBt ester 4, that was next converted into the highly crystalline di-depsidic dimer 5 upon treatment with DMAP. The mono-depsidic dimer 6 was also formed when the reaction was carried out with partially decarboxylated THCA-A samples. The structure of the depsidic dimers was established by spectroscopic methods and by aminolysis of 5 into the pre-cannabinoid amide 7. Both dimers showed excellent shelf stability and did not generate significant amounts of D9-THC upon heating. However, only the didepsidic dimer 5 activated PPAR-g, the major target of pre-cannabinoids, but strong binding to serum proteins abolished this activity, also shielding it from the action of esterases.
文摘Plants synthesize an astonishing diversity of isoprenoids,some of which play essential roles in photosynthesis,respiration,and the regulation of growth and development.Two independent pathways for the biosynthesis of isoprenoid precursors coexist within the plant cell: the cytosolic mevalonic acid (MVA) pathway and the plastidial methylerythritol phosphate (MEP) pathway.However,little is known about the effects of plant hormones on the regulation of these pathways.In the present study we investigated the effect of gibberellic acid (GA3) on changes in the amounts of many produced terpenoids and the activity of the key enzymes,1-deoxy-D-xylulose 5-phosphate synthase (DXS) and 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR),in these pathways.Our results showed GA3 caused a decrease in DXS activity in both sexes that it was accompanied by a decrease in chlorophylls,carotenoids and 9-tetrahydrocannabinol (THC) contents and an increase in α-tocopherol content.The treated plants with GA3 showed an increase in HMGR activity.This increase in HMGR activity was followed by accumulation of stigmasterol and β-sitosterol in male and female plants and campestrol in male plants.The pattern of the changes in the amounts of sterols was exactly similar to the changes in the HMGR activity.These data suggest that GA3 can probably influence the MEP and MVA pathways oppositely,with stimulatory and inhibitory effects on the produced primary terpenoids in MVA and DXS pathways,respectively.
文摘目的：建立气相色谱-质谱法同时分析运动营养品中大麻酚、大麻二酚和Δ9-四氢大麻酚的检测方法。方法：样品采用液液萃取,提取液经过正相固相萃取柱（Silica）纯化,洗脱液氮气吹干,N-甲基-N-（三甲基硅烷）三氟乙酰胺衍生化后,采用HP-1MS柱（17 m×0.2 mm i.d.×0.11 mm）色谱分离,程序升温,质谱检测,D3-Δ9-四氢大麻酚为内标。结果：大麻酚、大麻二酚和Δ9-四氢大麻酚的衍生化产物实现基线分离,三个定性特征离子的峰度比计算结果可以满足世界反兴奋剂机构（WADA）要求。该方法的检测限为1μg/kg,定量限为2μg/kg,在添加的高、中、低三种浓度的相对回收率分布在94%~119%之间。结论：该方法满足常规检测要求,样品前处理简单、快速、可靠。
