Worldwide, there are plants known as psychoactive plants that naturally contain psychedelic active components. They have a high concentration of neuroprotective substances that can interact with the nervous system to produce psychedelic effects. Despite these plants' hazardous potential, recreational use of them is on the rise because of their psychoactive properties. Early neuroscience studies relied heavily on psychoactive plants and plant natural products (NPs), and both recreational and hazardous NPs have contributed significantly to the understanding of almost all neurotransmitter systems. Worldwide, there are many plants that contain psychoactive properties, and people have been using them for ages. Psychoactive plant compounds may significantly alter how people perceive the world.
1. Plants (Basel). 2024 Sep 18;13(18):2599. doi: 10.3390/plants13182599. Spatio-Temporal Variations of Volatile Metabolites as an Eco-Physiological Response of a Native Species in the Tropical Forest. Felisberto JS(1)(2)(3), Machado DB(1)(2), Assunção JAS(4), Massau SAS(2), Queiroz GA(5), Guimarães EF(2), Ramos YJ(1)(3), Moreira DL(1)(2)(4). Author information: (1)Postgraduate Program in Plant Biology, State University of Rio de Janeiro, Maracanã, Rio de Janeiro 20550-013, RJ, Brazil. (2)Natural Products and Biochemistry Laboratory, Rio de Janeiro Botanical Garden Research Institute, Jardim Botânico, Rio de Janeiro 22460-030, RJ, Brazil. (3)Earth's Pharmacy Laboratory, Federal University of Bahia, Ondina, Salvador 40170-215, BA, Brazil. (4)Postgraduate Program in Translational Research in Drugs and Medicines, Pharmaceutical Technology Institute (Farmanguinhos), Oswaldo Cruz Foundation, Rio de Janeiro 21041-250, RJ, Brazil. (5)Department of Pharmacy, State University of Rio de Janeiro, Rio de Janeiro 23070-200, RJ, Brazil. This study evaluates the essential oil (EO) composition of Piper rivinoides Kunth, a shrub native to the Brazilian tropical rainforest, across different plant parts and developmental phases. The aim was to explore the chemical diversity of EO and its reflection in the plant's ecological interactions and adaptations. Plant organs (roots, stems, branches, and leaves) at different developmental phases were subjected to hydrodistillation followed by chemical analysis using Gas Chromatography-Mass Spectrometry (GC-MS) and Gas Chromatography-Flame Ionization Detector (GC-FID). The results revealed a relevant variation in EO yield and composition among different plant parts and developmental phases. Leaves showed the highest yield and chemical diversity, with α-pinene and β-pinene as major constituents, while roots and stems were characterized by a predominance of arylpropanoids, particularly apiol. The chemical diversity in leaves increased with plant maturity, indicating a dynamic adaptation to environmental interactions. The study underscores the importance of considering the ontogeny of plant parts in understanding the ecological roles and potential applications of P. rivinoides in medicine and agriculture. The findings contribute to the overall knowledge of Piperaceae chemodiversity and ecological adaptations, offering insights into the plant's interaction with its environment and its potential uses based on chemical composition. DOI: 10.3390/plants13182599 PMCID: PMC11435382 PMID: 39339574 Conflict of interest statement: The authors declare no conflicts of interest. 2. Heliyon. 2024 Aug 30;10(17):e36866. doi: 10.1016/j.heliyon.2024.e36866. eCollection 2024 Sep 15. Hepato-renal protective impact of nanocapsulated Petroselinum crispum and Anethum graveolens essential oils added in fermented milk against some food additives via antioxidant and anti-inflammatory effects: In silico and in vivo studies. Mohamed RS(1), Fouda K(1), Maghraby AS(2), Assem FM(3), Menshawy MM(4), Zaghloul AH(3), Abdel-Salam AM(3). Author information: (1)Nutrition and Food Sciences Department, National Research Centre, Dokki, Cairo, Egypt. (2)Department of Therapeutic Chemistry, research group immune-and bio-markers for infection, the Center of Excellent for Advanced Science (CEAS), National Research Centre, Dokki, Cairo, Egypt. (3)Dairy Science Department, National Research Centre, Dokki, Cairo, Egypt. (4)College of Pharmaceutical Sciences and Drug Manufacturing, Misr University for Science and Technology, 6th October City, Egypt. The study assessed the efficacy of parsley and dill essential oils (EOs) nanocapsules incorporated into fermented milk in hepato-renal protection against specific food additives. A molecular docking assay was conducted between parsley and dill EOs bioactive molecules and inflammatory cytokines. Freeze-dried parsley and dill EOs nanocapsules were developed, characterized for their morphological structure, particle size, zeta potential, polydispersity index and encapsulation efficiency and assessed in fast green dye and sodium benzoate (SB) combination-treated rats. The docking results revealed that the primary constituents of parsley and dill EOs (apiol, myristicin, α-pinene, (-)-carvone, and d-limonene) interacted with the active sites of TNF-α, IL-1β and TGF-1β cytokines with hydrophobic and hydrogen bond interactions. D-limonene had the highest binding affinity (6.4 kcal/mol) for the TNF-α. Apiol and myristicin had the highest binding affinity (5.1, 5.0, 5.0 and 5.0 kcal/mol, respectively) for the IL-1β and TGF-β1 receptors. Biochemically and histopathologically, the excessive co-administration of fast green and SB revealed adverse effects on the liver and the kidney. Whereas the treatment with parsley and dill EOs nanocapsules afford hepato-renal protective effects as manifested by suppression the elevated liver and kidney functions. Parsley and dill EOs nanocapsules showed a significant reduction of the liver (64.08 and 80.5 pg/g, respectively) and kidney (59.3 and 83.6 pg/g, respectively) ROS. Moreover, parsley and dill EOs nanocapsules down-regulated the liver and the kidney inflammatory cytokines (IL-6, TNF-α, IL-1β and TGF-1β) and lipid peroxidation and up-regulated the antioxidant enzymes. In conclusion, the data suggest a potential hepato-renal protective effects of parsley and dill EOs nanocapsules. © 2024 The Author(s). DOI: 10.1016/j.heliyon.2024.e36866 PMCID: PMC11403541 PMID: 39286161 Conflict of interest statement: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. 3. Mutat Res. 2024 Aug 16;829:111881. doi: 10.1016/j.mrfmmm.2024.111881. Online ahead of print. Apiole, an important constituent of parsley, is a mixed-type inhibitor of the CYP1A subfamily. Espinosa-Aguirre JJ(1), Camacho-Carranza R(2), Hernández-Ojeda SL(3), Cárdenas-Ávila RI(4), Santes-Palacios R(5). Author information: (1)Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Tercer Circuito Exterior sin Número, Ciudad Universitaria, Ciudad de México 04510, Mexico. Electronic address: jjea@iibiomedicas.unam.mx. (2)Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Tercer Circuito Exterior sin Número, Ciudad Universitaria, Ciudad de México 04510, Mexico. Electronic address: rcamacho@iibiomedicas.unam.mx. (3)Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Tercer Circuito Exterior sin Número, Ciudad Universitaria, Ciudad de México 04510, Mexico. (4)Facultad de Ciencias, Universidad Nacional Autónoma de México, Avenida Universidad 3000, Ciudad de México 04510, Mexico. (5)Laboratorio de Toxicología Genética, Instituto Nacional de Pediatría, Insurgentes Sur 3700-C, Insurgentes Cuicuilco, Coyoacán, Ciudad de México C. P. 04530, Mexico. Apiole (1-allyl-2,5-dimethoxy-3,4-methylenedioxybenzene) and parsley leaves ethanolic extract containing it inhibit the rat liver microsomal ethoxy- and methoxyresorufin-O-deacetylase activities associated with cytochrome P450 (CYP) 1A1 and 1A2, respectively. Cytochrome P4501A subfamily metabolizes environmental mutagens and several drugs, leading to the formation of mutagenic metabolites. Docking analysis showed that residue Phe123 within the active site of the CYP1A1 enzyme is bound to apiole through a π/π stacking of its benzene ring. In the case of 1A2, its Phe226 interacts with the dioxolane ring of apiole. Furthermore, apiole behaves as a mixed-type inhibitor of bacterial human recombinant CYP1A1. To explore one of the possible biological implications of this inhibitory effect, we tested the capacity of apiole and the parsley ethanolic extract to interfere with the mutagenicity of the promutagen 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) metabolized by CYP1A subfamily. As expected, both apiole and the plant extract reduced the number of revertant colonies of Salmonella typhimurium TA98 Ames strain after exposure to MeIQx, reaching a 78 % and 100 % reduction, respectively. Neither apiol nor parsley extract were mutagenic to the TA98 strain. We speculate that consuming apiole, a constituent of edible herbs, in conjunction with the utilization of pharmaceuticals metabolized by the CYP1A subfamily, may result in herb-drug interactions. Furthermore, the consumption of apiole by individuals who regularly ingest fresh vegetables may contribute to the low incidence of cancer observed in those who adhere to such a dietary regimen. Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved. DOI: 10.1016/j.mrfmmm.2024.111881 PMID: 39191149 Conflict of interest statement: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. 4. Heliyon. 2024 Jul 23;10(15):e34995. doi: 10.1016/j.heliyon.2024.e34995. eCollection 2024 Aug 15. Association analysis of leaf aromatic substances in cultivated and weedy types of Perilla crop using SSR markers. Cho J(1)(2), Sa KJ(3), Park H(1)(2), Heo TH(1)(2), Lee S(4), Lee JK(1)(2). Author information: (1)Department of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University, Chuncheon 24341, South Korea. (2)Interdisciplinary Program in Smart Agriculture, Kangwon National University, Chuncheon 24341, South Korea. (3)Department of Crop Science, College of Ecology & Environmental Sciences, Kyungpook National University, Sangju 37224, South Korea. (4)National Agrobiodiversity Center, National Institute of Agricultural Sciences, RDA, Jeonju 54874, South Korea. In East Asia, particularly South Korea, the two cultivated varieties of Perilla are commonly grown. They are clearly distinguished by their aromatic substances and have different uses as leafy vegetables or oil crop. This study was performed for the development of simple sequence repeat (SSR) markers linked to volatile compounds in Perilla leaves that show differences between cultivated var. frutescens (CF), weedy var. frutescens (WF), and weedy var. crispa (WC) of Perilla. Fifty Perilla SSR primer sets were used to analyze genetic diversity for the 80 Perilla accessions of the three types. A total of 276 alleles were detected, with an average of 5.5 alleles per locus. The average genetic diversity values for CF, WF, and WC accessions were 0.402, 0.583, and 0.437, respectively. WF accessions exhibited the highest genetic diversity among the three types of the Perilla crop. Phylogenetic tree analysis classified 80 Perilla accessions of the three types into four groups, showing 37.2 % genetic similarity. Three types of the Perilla crop were clearly distinguished except for outstanding accessions. Through the application of an association analysis involving 50 Perilla SSR primer sets and five volatile compounds (perilla aldehyde, perilla ketone, myristicin, dill apiol, (Z,E)-α-farnesene) in the three types of the Perilla accessions, we detected 11 significant marker-trait associations duplicated in both Q GLM and Q + K MLM methods. These findings serve as valuable insights for identifying the aromatic substances in Perilla plants originating from various regions of South Korea. © 2024 The Authors. DOI: 10.1016/j.heliyon.2024.e34995 PMCID: PMC11336293 PMID: 39170332 Conflict of interest statement: We declare that this manuscript is original, has not been published and is not under consideration for publication elsewhere and there are no conflicts of interest to disclose. 5. Parsley. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–. 2024 Aug 15. Parsley (Carum petroselinum) leaf, seed, and root contain the volatile oils apiol and myristicin, which is pharmacologically active, as well as flavonoids, beta-phellandrene, bergapten, and vitamins A and C. Warm compresses or poultices of parsley have been used to treat breast engorgement and mastalgia.[1,2] Oral capsules containing sage and parsley capsules are said to decrease milk flow; however, no scientifically valid clinical trials support this use. Some mothers in Türkiye reportedly use parsley to increase their milk supply.[3] Galactogogues should never replace evaluation and counseling on modifiable factors that affect milk production.[4,5] No data exist on the excretion of any components of parsley into breastmilk or on the safety and efficacy of parsley nursing mothers or infants. Parsley is "generally recognized as safe" (GRAS) as a food by the U.S. Food and Drug Administration. Adverse reactions are primarily allergic, including cross reactions to other members of the Apiaceae family, such as carrot, celery, and fennel. The essential oil should not be used because of potential toxicity of its apiol and myristicin content. Dietary supplements do not require extensive pre-marketing approval from the U.S. Food and Drug Administration. Manufacturers are responsible to ensure the safety, but do not need to prove the safety and effectiveness of dietary supplements before they are marketed. Dietary supplements may contain multiple ingredients, and differences are often found between labeled and actual ingredients or their amounts. A manufacturer may contract with an independent organization to verify the quality of a product or its ingredients, but that does not certify the safety or effectiveness of a product. Because of the above issues, clinical testing results on one product may not be applicable to other products. More detailed information about dietary supplements is available elsewhere on the LactMed Web site. PMID: 30000940