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Article: Mentha rotundifolia

Boualam, Khadija / Ibork, Hind / Lahboub, Zakaria / Sobeh, Mansour / Taghzouti, Khalid

2024 Volume 16, Page(s) 1365086

Abstract: Introduction: Aging is often linked to oxidative stress, where the body experiences increased damage from free radicals. Plants are rich sources of antioxidants, playing a role in slowing down aging and supporting the proper functioning and longevity of ...

Abstract	Introduction: Aging is often linked to oxidative stress, where the body experiences increased damage from free radicals. Plants are rich sources of antioxidants, playing a role in slowing down aging and supporting the proper functioning and longevity of cells. Our study focuses on exploring the impact of Methods: The chemical composition of MR and SO hydrosols was analyzed by gas chromatography coupled to mass spectrometry. 2,2-Diphenyl 1-picrylhydrazyl and 2,20-azino-bis 3-ethylbenzothiazoline-6-sulfonic acid radicals scavenging assays were used to assess their Results and discussion: At two years old, animals treated with MR and SO hydrosols displayed fewer physical and behavioral impairments, along with well-preserved redox homeostasis in comparison with animals in the control group. These results highlighted the significance of MR and SO hydrosols in addressing various aspects of age-related comorbidities. The study suggests that these plant-derived hydrosols may have potential applications in promoting healthy aging and mitigating associated health challenges.
Language	English
Publishing date	2024-02-23
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2558898-9
ISSN	1663-4365
ISSN	1663-4365
DOI	10.3389/fnagi.2024.1365086
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Article: Mentha rotundifolia

Boualam, Khadija / Bouhaddou, Nezha / Sobeh, Mansour / Tabyaoui, Mohamed / Taghzouti, Khalid

Frontiers in neuroscience

2023 Volume 17, Page(s) 1121029

Abstract: Introduction: Oxidative stress plays a causal role in neurodegenerative diseases. The aim of this study is to evaluate the antioxidant and neuroprotective effects of : Methods: The chemical composition of : Results and discussion: The LC-MS/MS ... ...

Abstract	Introduction: Oxidative stress plays a causal role in neurodegenerative diseases. The aim of this study is to evaluate the antioxidant and neuroprotective effects of Methods: The chemical composition of Results and discussion: The LC-MS/MS analysis revealed high content of kaempferol glucuronide (85%) at the extract. IC
Language	English
Publishing date	2023-03-09
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2411902-7
ISSN	1662-453X ; 1662-4548
ISSN (online)	1662-453X
ISSN	1662-4548
DOI	10.3389/fnins.2023.1121029
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Article ; Online: Restraint Stress Exacerbates Apoptosis in a 6-OHDA Animal Model of Parkinson Disease.

Idrissi, Sara El / Fath, Nada / Ibork, Hind / Taghzouti, Khalid / Alamy, Meryem / Abboussi, Oualid

Neurotoxicity research

2023 Volume 41, Issue 2, Page(s) 166–176

Abstract: Activation of the apoptotic pathway has been associated with promoting neuronal cell death in the pathophysiology of Parkinson disease (PD). Nonetheless, the mechanisms by which it may occur remain unclear. It has been suggested that stress-induced ... ...

Abstract	Activation of the apoptotic pathway has been associated with promoting neuronal cell death in the pathophysiology of Parkinson disease (PD). Nonetheless, the mechanisms by which it may occur remain unclear. It has been suggested that stress-induced oxidation and potential apoptosis may play a major role in the progression of PD. Thus, in this study, we aimed to investigate the effect of subchronic restraint stress on striatal dopaminergic activity, iron, p53, caspase-3, and plasmatic acetylcholinesterase (AChE) levels in male Wistar rat model of PD induced by administration of 6-hydroxydopamine (6-OHDA) in the medial forebrain bundle (MFB). The obtained results showed that restraint stress exacerbates motor coordination deficits and anxiety in animals treated with 6-OHDA in comparison to animals receiving saline, and it had no effect on object recognition memory. On another hand, 6-OHDA decreased dopamine (DA) levels, increased iron accumulation, and induced overexpression of the pro-apoptotic factors caspase-3, p53, and AChE. More interestingly, post-lesion restraint stress exacerbated the expression of caspase-3 and AChE without affecting p53 expression. These findings suggest that subchronic stress may accentuate apoptosis and may contribute to DA neuronal loss in the striatal regions and possibly exacerbate the progression of PD.
MeSH term(s)	Rats ; Animals ; Male ; Parkinson Disease/metabolism ; Oxidopamine/toxicity ; Caspase 3/metabolism ; Acetylcholinesterase/metabolism ; Tumor Suppressor Protein p53 ; Rats, Wistar ; Dopamine/metabolism ; Disease Models, Animal ; Apoptosis
Chemical Substances	Oxidopamine (8HW4YBZ748) ; Caspase 3 (EC 3.4.22.-) ; Acetylcholinesterase (EC 3.1.1.7) ; Tumor Suppressor Protein p53 ; Dopamine (VTD58H1Z2X)
Language	English
Publishing date	2023-01-12
Publishing country	United States
Document type	Journal Article
ZDB-ID	2036826-4
ISSN	1476-3524 ; 1029-8428
ISSN (online)	1476-3524
ISSN	1029-8428
DOI	10.1007/s12640-022-00630-3
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Article ; Online: Almond oil: A comprehensive review of chemical composition, extraction methods, preservation conditions, potential health benefits, and safety.

Ouzir, Mounir / Bernoussi, Sara El / Tabyaoui, Mohamed / Taghzouti, Khalid

Comprehensive reviews in food science and food safety

2021 Volume 20, Issue 4, Page(s) 3344–3387

Abstract: Almond oil, a rich source of macronutrients and micronutrients, is extracted for food flavorings and the cosmetics industry. In recent years, the need for high-quality and high-quantity production of almond oil for human consumption has been increased. ... ...

Abstract	Almond oil, a rich source of macronutrients and micronutrients, is extracted for food flavorings and the cosmetics industry. In recent years, the need for high-quality and high-quantity production of almond oil for human consumption has been increased. The present review examines the chemical composition of almond oil, storage conditions, and clinical evidence supporting the health benefits of almond oil. From the reviewed studies, it appears that almond oil contains a significant proportion of poly and monounsaturated fatty acids, with oleic acid as the main compound, and an important amount of tocopherol and phytosterol content. Some variations in almond oil composition can be found depending on the kernel's origin and the extraction system used. Some new technologies such as ultrasonic-assisted extraction, supercritical fluid extraction, subcritical fluid extraction, and salt-assisted aqueous extraction have emerged as the most promising extraction techniques that allow eco-friendly and effective recovery of almond oil. This safe oil was reported by several clinical studies to have potential roles in cardiovascular risk management, glucose homeostasis, oxidative stress reduction, neuroprotection, and many dermatologic and cosmetic applications. However, the anticarcinogenic and fertility benefits of almond oil have yet to be experimentally verified.
MeSH term(s)	Chromatography, Supercritical Fluid ; Cosmetics ; Humans ; Plant Oils ; Water
Chemical Substances	Cosmetics ; Plant Oils ; Water (059QF0KO0R) ; almond oil (66YXD4DKO9)
Language	English
Publishing date	2021-05-30
Publishing country	United States
Document type	Journal Article ; Review
ZDB-ID	2185829-9
ISSN	1541-4337 ; 1541-4337
ISSN (online)	1541-4337
ISSN	1541-4337
DOI	10.1111/1541-4337.12752
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Article ; Online: Pathophysiology and immunogenetics of celiac disease.

Aboulaghras, Sara / Piancatelli, Daniela / Oumhani, Khadija / Balahbib, Abdelaali / Bouyahya, Abdelhakim / Taghzouti, Khalid

Clinica chimica acta; international journal of clinical chemistry

2022 Volume 528, Page(s) 74–83

Abstract: Celiac disease (CD) is a chronic inflammatory enteropathy caused by gluten (protein from wheat, rye and, barley) in genetically predisposed individuals carrying the HLA-DQ2/HLA-DQ8 genotype. This pathology has a multifactorial etiology in which HLA genes, ...

Abstract	Celiac disease (CD) is a chronic inflammatory enteropathy caused by gluten (protein from wheat, rye and, barley) in genetically predisposed individuals carrying the HLA-DQ2/HLA-DQ8 genotype. This pathology has a multifactorial etiology in which HLA genes, the microbiome, gluten and, other environmental factors are involved in the development of the disease. Its pathogenesis involves both innate and adaptive immunity as well as upregulation of IL-15. The objective of this review is to examine the results of current studies on genetic and environmental variables to better understand the pathogenesis of this enteropathy. The complex etiology of celiac disease makes our understanding of the pathogenesis of the disease incomplete, and a better knowledge of the many genetic and environmental components would help us better understand the pathophysiology of celiac disease.
MeSH term(s)	Celiac Disease/genetics ; Genetic Predisposition to Disease ; Glutens/genetics ; HLA-DQ Antigens/genetics ; Humans ; Immunogenetics
Chemical Substances	HLA-DQ Antigens ; Glutens (8002-80-0)
Language	English
Publishing date	2022-02-01
Publishing country	Netherlands
Document type	Journal Article ; Review
ZDB-ID	80228-1
ISSN	1873-3492 ; 0009-8981
ISSN (online)	1873-3492
ISSN	0009-8981
DOI	10.1016/j.cca.2022.01.022
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Article ; Online: CB2 agonist mitigates cocaine-induced reinstatement of place preference and modulates the inflammatory response in mice.

Abboussi, Oualid / Khan, Zmarak Ahmad / Ibork, Hind / Zulu, Simo S / Daniels, William / Taghzouti, Khalid / Hales, Tim G

Behavioural pharmacology

2023 Volume 35, Issue 1, Page(s) 26–35

Abstract: Chronic exposure to cocaine is known to have profound effects on the brain, leading to the dysregulation of inflammatory signalling pathways, the activation of microglia, and the manifestation of cognitive and motivational behavioural impairments. The ... ...

Abstract	Chronic exposure to cocaine is known to have profound effects on the brain, leading to the dysregulation of inflammatory signalling pathways, the activation of microglia, and the manifestation of cognitive and motivational behavioural impairments. The endocannabinoid system has emerged as a potential mediator of cocaine's deleterious effects. In this study, we sought to investigate the therapeutic potential of the cannabinoid CB2 receptor agonist, JWH-133, in mitigating cocaine-induced inflammation and associated motivational behavioural alterations in an in vivo model. Our research uncovered compelling evidence that JWH-133, a selective CB2 receptor agonist, exerts a significant dampening effect on the reinstatement of cocaine-induced conditioned place preference. This effect was accompanied by notable changes in the neurobiological landscape. Specifically, JWH-133 administration was found to upregulate Δ-FOSB expression in the nucleus accumbens (Nac), elevate CX3CL1 levels in both the ventral tegmental area and prefrontal cortex (PFC), and concurrently reduce IL-1β expression in the PFC and NAc among cocaine-treated animals. These findings highlight the modulatory role of CB2 cannabinoid receptor activation in altering the reward-seeking behaviour induced by cocaine. Moreover, they shed light on the intricate interplay between the endocannabinoid system and cocaine-induced neurobiological changes, paving the way for potential therapeutic interventions targeting CB2 receptors in the context of cocaine addiction and associated behavioural deficits.
MeSH term(s)	Mice ; Animals ; Endocannabinoids/metabolism ; Receptor, Cannabinoid, CB2 ; Cocaine/pharmacology ; Cocaine/metabolism ; Cannabinoids/pharmacology ; Nucleus Accumbens/metabolism ; Cannabinoid Receptor Agonists/pharmacology
Chemical Substances	1,1-dimethylbutyl-1-deoxy-Delta(9)-THC (TDG8048RDA) ; Endocannabinoids ; Receptor, Cannabinoid, CB2 ; Cocaine (I5Y540LHVR) ; Cannabinoids ; Cannabinoid Receptor Agonists
Language	English
Publishing date	2023-12-13
Publishing country	England
Document type	Journal Article
ZDB-ID	1027374-8
ISSN	1473-5849 ; 0955-8810
ISSN (online)	1473-5849
ISSN	0955-8810
DOI	10.1097/FBP.0000000000000759
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Article ; Online: Effect of Cannabidiol in LPS-Induced Toxicity in Astrocytes: Possible Role for Cannabinoid Type-1 Receptors.

Ibork, Hind / Idrissi, Sara El / Zulu, Simo Siyanda / Miller, Robert / Hajji, Lhoussain / Morgan, Annabelle Manalo / Taghzouti, Khalid / Abboussi, Oualid

Neurotoxicity research

2023 Volume 41, Issue 6, Page(s) 615–626

Abstract: Cerebral metabolic abnormalities are common in neurodegenerative diseases. Previous studies have shown that mitochondrial damage alters ATP production and increases reactive oxygen species (ROS) release which may contribute to neurodegeneration. In the ... ...

Abstract	Cerebral metabolic abnormalities are common in neurodegenerative diseases. Previous studies have shown that mitochondrial damage alters ATP production and increases reactive oxygen species (ROS) release which may contribute to neurodegeneration. In the present study, we investigated the neuroprotective effects of cannabidiol (CBD), a non-psychoactive component derived from marijuana (Cannabis sativa L.), on astrocytic bioenergetic balance in a primary cell culture model of lipopolysaccharide (LPS)-induced neurotoxicity. Astrocytic metabolic profiling using an extracellular flux analyzer demonstrated that CBD decreases mitochondrial proton leak, increased spare respiratory capacity and coupling efficiency in LPS-stimulated astrocytes. Simultaneously, CBD increased astrocytic glycolytic capacity and glycolysis reserve in a cannabinoid receptor type 1 (CB1)-dependent manner. CBD-restored metabolic changes were correlated with a significant decrease in the pro-inflammatory cytokines tumor necrosis factor α (TNFα) and interleukin-6 (IL-6) concentration and reduction of ROS production in LPS-stimulated astrocytes. These results suggest that CBD may inhibit LPS-induced metabolic impairments and inflammation by enhancing astrocytic metabolic glycolysis versus oxidative phosphorylation through its action on CB1 receptors. The present findings suggest CBD as a potential anti-inflammatory treatment in metabolic pathologies and highlight a possible role for the cannabinoidergic system in the modulation of mitochondrial oxidative stress. CBD enhances mitochondrial bioenergetic profile, attenuates proinflammatory cytokines release, and ROS overproduction of astrocytes stimulated by LPS. These effects are not mediated directly by CB1 receptors, while these receptors seem to have a key role in the anti-inflammatory response of the endocannabinoid system on astrocytes, as their specific inhibition by SR141716A led to increased pro-inflammatory cytokines release and ROS production. The graphical abstract is created with BioRender.com.
MeSH term(s)	Cannabidiol/pharmacology ; Lipopolysaccharides/toxicity ; Receptors, Cannabinoid/metabolism ; Reactive Oxygen Species/metabolism ; Astrocytes ; Cytokines ; Anti-Inflammatory Agents/pharmacology
Chemical Substances	Cannabidiol (19GBJ60SN5) ; Lipopolysaccharides ; Receptors, Cannabinoid ; Reactive Oxygen Species ; Cytokines ; Anti-Inflammatory Agents
Language	English
Publishing date	2023-10-02
Publishing country	United States
Document type	Journal Article
ZDB-ID	2036826-4
ISSN	1476-3524 ; 1029-8428
ISSN (online)	1476-3524
ISSN	1029-8428
DOI	10.1007/s12640-023-00671-2
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Article: Almond oil: A comprehensive review of chemical composition, extraction methods, preservation conditions, potential health benefits, and safety

Ouzir, Mounir / Bernoussi, Sara El / Tabyaoui, Mohamed / Taghzouti, Khalid

Comprehensive reviews in food science and food safety. 2021 July, v. 20, no. 4

2021

Abstract: Almond oil, a rich source of macronutrients and micronutrients, is extracted for food flavorings and the cosmetics industry. In recent years, the need for high‐quality and high‐quantity production of almond oil for human consumption has been increased. ... ...

Abstract	Almond oil, a rich source of macronutrients and micronutrients, is extracted for food flavorings and the cosmetics industry. In recent years, the need for high‐quality and high‐quantity production of almond oil for human consumption has been increased. The present review examines the chemical composition of almond oil, storage conditions, and clinical evidence supporting the health benefits of almond oil. From the reviewed studies, it appears that almond oil contains a significant proportion of poly and monounsaturated fatty acids, with oleic acid as the main compound, and an important amount of tocopherol and phytosterol content. Some variations in almond oil composition can be found depending on the kernel's origin and the extraction system used. Some new technologies such as ultrasonic‐assisted extraction, supercritical fluid extraction, subcritical fluid extraction, and salt‐assisted aqueous extraction have emerged as the most promising extraction techniques that allow eco‐friendly and effective recovery of almond oil. This safe oil was reported by several clinical studies to have potential roles in cardiovascular risk management, glucose homeostasis, oxidative stress reduction, neuroprotection, and many dermatologic and cosmetic applications. However, the anticarcinogenic and fertility benefits of almond oil have yet to be experimentally verified.
Keywords	almond oil ; chemical composition ; cosmetics ; food safety ; glucose ; homeostasis ; humans ; industry ; neuroprotective effect ; oleic acid ; oxidative stress ; phytosterols ; risk management ; seeds ; supercritical fluid extraction
Language	English
Dates of publication	2021-07
Size	p. 3344-3387.
Publishing place	John Wiley & Sons, Ltd
Document type	Article
Note	JOURNAL ARTICLE
ZDB-ID	2185829-9
ISSN	1541-4337
ISSN	1541-4337
DOI	10.1111/1541-4337.12752
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Article ; Online: Chronic Exposure to WIN55,212-2 During Adolescence Alters Prefrontal Dopamine Turnover and Induces Sensorimotor Deficits in Adult Rats.

Abboussi, Oualid / Andaloussi, Zineb Ibn Lahmar / Chris, Ajonijebu Duyilemi / Taghzouti, Khalid

Neurotoxicity research

2020 Volume 38, Issue 3, Page(s) 682–690

Abstract: Several lines of evidence suggest that chronic exposure to cannabinoids during adolescence may increase the risk of schizophrenia. Studies of the disorder have identified altered cortical dopaminergic neurotransmission. In this study, we hypothesised ... ...

Abstract	Several lines of evidence suggest that chronic exposure to cannabinoids during adolescence may increase the risk of schizophrenia. Studies of the disorder have identified altered cortical dopaminergic neurotransmission. In this study, we hypothesised that heightened endocannabinoid system activation via chronic exposure to a highly potent cannabinoid receptors agonist in adolescent rats would cause long-lasting neurobiological changes that may dramatically alter expression and functions of dopamine metabolising enzymes, comethyl-o-transferase (COMT) and monoamine oxidases MAO-A and MAO-B. To test this hypothesis, adult male rats (70 PND) undergoing chronic treatment of the highly potent and non-selective CB agonist WIN55,212-2 (1.2 mg/kg) during adolescence (PND 30-50) were subjected after 20 days washout period to prepulse inhibition of acoustic startle test (PPI) to confirm cannabinoid-induced sensorimotor-gating impairments and afterwards examined for COMT, MAO-A and MAO-B expression and activity in the prefrontal cortex. Chronic WIN55,212-2 exposure during adolescence caused disruption of PPI, increased cortical dopamine level, decreased COMT mRNA expression and decreased MAO-A and MAO-B enzymatic activities. These results indicate that chronic exposure to cannabinoids during adolescence induces sensorimotor-gating alterations which likely result from changes in the prefrontal cortex dopaminergic signalling. This has important implications for developing methods of targeting dopamine metabolising enzymes and/or sequelae of its dysregulation in cannabinoid-induced schizoaffective-like behaviour.
Language	English
Publishing date	2020-08-05
Publishing country	United States
Document type	Journal Article
ZDB-ID	2036826-4
ISSN	1476-3524 ; 1029-8428
ISSN (online)	1476-3524
ISSN	1029-8428
DOI	10.1007/s12640-020-00266-1
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Article ; Online: Acute cannabidiol treatment attenuates ethanol-induced place preference and reduces aggressivity in group-housed male rats.

Andaloussi, Zineb Ibn Lahmar / Lauer, Wendy / Zulu, Simo S / Taghzouti, Khalid / Abboussi, Oualid

Pharmacology, biochemistry, and behavior

2021 Volume 211, Page(s) 173290

Abstract: Alcohol abuse is a widespread cause of aggressive and impulsive behaviors that impact the users as well as their entourage. However, only a few medications are effective. Recently, cannabidiol has been reported to improve mood disorders and recovery from ...

Abstract	Alcohol abuse is a widespread cause of aggressive and impulsive behaviors that impact the users as well as their entourage. However, only a few medications are effective. Recently, cannabidiol has been reported to improve mood disorders and recovery from substance abuse, yet the psychopharmacologic effects of cannabidiol in ethanol-induced drug reward and aggressivity remain unexplored. In the present study, we investigated the effects of cannabidiol on ethanol-induced place preference and aggressivity in individually and group-housed male rats using the conditioned place preference test, and intruder evoc aggression test, respectively. The obtained results showed that ethanol significantly increased locomotor activity, induced conditioned place preference in all animals, and, specifically, increased aggressivity in individually housed rats. These behavioural impairments induced by ethanol were associated with decreased glucocorticoid and mineralocorticoid receptors transcription in the prefrontal cortex. Notwithstanding, cannabidiol at a dose of 10 mg/kg significantly inhibited Et-OH-induced place preference in group-housed, but not in individually housed rats, and markedly inhibited the aggressive behaviour. These findings suggest that ethanol-induced behavioural impairments are dependent on the housing condition that may affect corticosterone receptors expression and subsequently the animal responsivity to cannabidiol treatment.
MeSH term(s)	Aggression/drug effects ; Animals ; Behavior, Animal/drug effects ; Cannabidiol/pharmacology ; Conditioning, Classical/drug effects ; Ethanol/pharmacology ; Housing, Animal ; Locomotion/drug effects ; Male ; Prefrontal Cortex/metabolism ; Rats ; Rats, Wistar ; Reward
Chemical Substances	Cannabidiol (19GBJ60SN5) ; Ethanol (3K9958V90M)
Language	English
Publishing date	2021-10-16
Publishing country	United States
Document type	Journal Article
ZDB-ID	191042-5
ISSN	1873-5177 ; 0091-3057
ISSN (online)	1873-5177
ISSN	0091-3057
DOI	10.1016/j.pbb.2021.173290
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