<Home — Psychoactive Plant Database



  Psychoactive Plant Database - Neuroactive Phytochemical Collection





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. Fitoterapia. 2024 Oct;178:106132. doi: 10.1016/j.fitote.2024.106132. Epub 2024 Jul 30. Relationship between the root processing method and quality of herbal medicine of Rauvolfia serpentina cultivated in Japan. Sugimura K(1), Katsuki S(2), Arai R(3), Kamiya H(3), Kawasaki T(3), Iida O(2), Kawahara N(2), Shrestha SS(4), Dall'Acqua S(5), Watanabe T(6). Author information: (1)Research Center for Medicinal Plant Resources, National Institutes of Biomedical Innovation, Health and Nutrition (NIBIOHN), 17007-2, Matsubarayama, Noma, Nakatane-cho, Kumage-gun, Kagoshima 891-3604, Japan; Department of Medicinal Plant, Faculty of Life Sciences, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan. (2)Research Center for Medicinal Plant Resources, National Institutes of Biomedical Innovation, Health and Nutrition (NIBIOHN), 17007-2, Matsubarayama, Noma, Nakatane-cho, Kumage-gun, Kagoshima 891-3604, Japan. (3)Uchida Wakanyaku Co., Ltd., 4-3-4 Higashi-nippori, Arakawa-ku, Tokyo 116-8571, Japan. (4)Himalayan Research and Development Center Nepal, Kathmandu, Nepal. (5)Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Italy. (6)Department of Medicinal Plant, Faculty of Life Sciences, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan. Electronic address: wtakashi@kumamoto-u.ac.jp. Rauvolfia serpentina roots are used as herbal medicine for snake and insect bites, fever, malaria, abdominal pain, hypertension, and dysentery in Southeast Asian countries. This study evaluates the content of reserpine, ajmaline, and ajmalicine in R. serpentina roots obtained with an efficient root processing method. The plants were cultivated in Tanegashima Island in southern part of Japan, where NIBIOHN's experimental farm station is located. We examined both the type of cork layer removal method (manual work, drum mixer washing, and high-pressure washing) and dried roots. We found that the resulting active ingredient contents were not significantly different between manual work and 30 min of drum mixer washing, and high-pressure washing. The washing in a drum mixer for 30 min could be an efficient root processing method. The amount of each active ingredient was compared in each root part (large-, middle-, and small-diameter roots), and there were no significant difference in their contents. In conclusion, R. serpentina roots having a diameter ≥ 0.5 cm contain a similar amount of active ingredients, suggesting that the quality of the crude drug does not vary in the root part. Thus, our study provides significant insights into the use of R. serpentina roots for herbal medicine applications as well as constituents of active ingredients. Copyright © 2024 Elsevier B.V. All rights reserved. DOI: 10.1016/j.fitote.2024.106132 PMID: 39089593 [Indexed for MEDLINE] Conflict of interest statement: Declaration of competing interest The authors report no conflict of interest. 2. Nat Prod Res. 2024 May 20:1-5. doi: 10.1080/14786419.2024.2354861. Online ahead of print. Chemical composition and antioxidant activity of the Amazonian fruit Ambelania acida Aubl. da Silva YC(1), da Silva Gomes G(2), Antonio ADS(3), Pimentel Rosado C(4), Pereira HMG(3), Kazumy de Lima Yamaguchi K(2), Teodoro AJ(5), da Veiga Júnior VF(1). Author information: (1)Chemical Engineering Section, Military Institute of Engineering, Rio de Janeiro, RJ, Brazil. (2)Institute of Health and Biotechnology, Federal University of Amazonas, Coari, AM, Brazil. (3)Laboratory for the Support of Technological Development, Chemistry Institute, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil. (4)Nutrition School, Federal University of the State of Rio de Janeiro, Rio de Janeiro, RJ, Brazil. (5)Faculty of Nutrition, Fluminense Federal University Rio de Janeiro, Rio de Janeiro, RJ, Brazil. Aqueous and hydroalcoholic extracts from the pulp of Ambelania acida Aubl. (Apocynaceae) fruits were subjected to analysis through UHPLC-HRMS and antioxidant potential using the TPC, DPPH, ABTS, FRAP, and ORAC assays. A putative identification of the compounds carried out by comparison of the fragmentation spectra revealed the predominance of the monoterpene indole alkaloids tabersonine, pseudocopsinine, ajmalicine, and strictosidine. Additionally, gallic acid, caffeic acid, citric acid, 3-O-p-coumaroylquinic acid, chlorogenic acid, catechin, ellagic acid, eschweilenol C (ellagic acid deoxyhexoside), and sucrose were identified. In face of the phenolic compounds observed, hydroalcoholic extract showed a higher antioxidant activity compared to the aqueous extract, observed at TPC (108.85 mg GAE/100g), FRAP (0.73 µmol Fe2SO4/g), DPPH (1221.76 µmol TE/g), ABTS (3460.00 µmol TE/g), and ORAC assays (120.47 µmol TE/g). These findings underscore the abundant presence of bioactive compounds, including phenolics and alkaloids, in an edible Amazonian fruit. DOI: 10.1080/14786419.2024.2354861 PMID: 38767203 3. Planta. 2023 Dec 27;259(2):30. doi: 10.1007/s00425-023-04311-z. Modulation of terpenoid indole alkaloid pathway via elicitation with phytosynthesized silver nanoparticles for the enhancement of ajmalicine, a pharmaceutically important alkaloid. Verma SK(1)(2), Goyary D(3), Singh AK(2), Anandhan S(4), Raina SN(5), Pandey S(6), Kumar S(7), Khare N(8). Author information: (1)Nims Institute of Allied Medical Science and Technology, Nims University Rajasthan, Delhi-Jaipur Highway, NH-11C, Jaipur, 303121, Rajasthan, India. (2)National Bureau of Plant Genetic Resources, Pusa Campus, New Delhi, 110012, India. (3)Division of Pharmaceutical Technology, Defence Research Laboratory, Tezpur, Assam, India. (4)ICAR-Directorate of Onion and Garlic Research, Rajgurunagar, Pune, 410505, Maharashtra, India. (5)Amity Institute of Biotechnology, Amity University Uttar Pradesh, Uttar Pradesh, Sector 125, Noida, 201313, India. (6)School of Bioengineering and Food Technology, Faculty of Applied Sciences and Biotechnology, Shoolini University, Solan, 173229, Himachal Pradesh, India. (7)National Centre for Cell Science, Ganeshkhind, Pune, 411007, Maharashtra, India. (8)Nims Institute of Allied Medical Science and Technology, Nims University Rajasthan, Delhi-Jaipur Highway, NH-11C, Jaipur, 303121, Rajasthan, India. neerajsnkhare@gmail.com. The use of silver nanoparticles as elicitors in cell cultures of Rauwolfia serpentina resulted in increased levels of ajmalicine, upregulated structural and regulatory genes, elevated MDA content, and reduced activity of antioxidant enzymes. These findings hold potential for developing a cost-effective method for commercial ajmalicine production. Plants possess an intrinsic ability to detect various stress signals, prompting the activation of defense mechanisms through the reprogramming of metabolites to counter adverse conditions. The current study aims to propose an optimized bioprocess for enhancing the content of ajmalicine in Rauwolfia serpentina callus through elicitation with phytosynthesized silver nanoparticles. Initially, callus lines exhibiting elevated ajmalicine content were established. Following this, a protocol for the phytosynthesis of silver nanoparticles using seed extract from Rauwolfia serpentina was successfully standardized. The physicochemical attributes of the silver nanoparticles were identified, including their spherical shape, size ranging from 6.7 to 28.8 nm in diameter, and the presence of reducing-capping groups such as amino, carbonyl, and amide. Further, the findings indicated that the presence of 2.5 mg L-1 phytosynthesized silver nanoparticles in the culture medium increased the ajmalicine content. Concurrently, structural genes (TDC, SLS, STR, SGD, G10H) and regulatory gene (ORCA3) associated with the ajmalicine biosynthetic pathway were observed to be upregulated. A notable increase in MDA content and a decrease in the activities of antioxidant enzymes were observed. A notable increase in MDA content and a decrease in the activities of antioxidant enzymes were also observed. Our results strongly recommend the augmentation of ajmalicine content in the callus culture of R. serpentina through supplementation with silver nanoparticles, a potential avenue for developing a cost-effective process for the commercial production of ajmalicine. © 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. DOI: 10.1007/s00425-023-04311-z PMID: 38150044 [Indexed for MEDLINE] 4. Org Lett. 2024 Jan 12;26(1):274-279. doi: 10.1021/acs.orglett.3c03972. Epub 2023 Dec 22. Combination of Machine Learning and Empirical Computation for the Structural Validation of Trirosaline, a Natural Trimeric Monoterpene Indole Alkaloid from Catharanthus roseus. Szwarc S(1), Jagora A(1), Derbré S(2), Leblanc K(1), Rharrabti S(1), Said-Hassane C(3), El Kalamouni C(3), Gallard JF(4), Le Pogam P(1), Beniddir MA(1). Author information: (1)Équipe "Chimie des Substances Naturelles" Université Paris-Saclay, CNRS, BioCIS, 17 avenue des Sciences, 91400 Orsay, France. (2)Université Angers, SONAS, SFR QUASAV, Faculty of Health Sciences, Department of Pharmacy, 16 Bd Daviers, 49045 CEDEX 01 Angers, France. (3)Unité Mixte Processus Infectieux en Milieu Insulaire Tropical, Université de la Réunion, INSERM U1187, CNRS UMR 9192, IRD UMR 249, Plateforme Technologique CYROI, 97490 Sainte Clotilde, La Réunion, France. (4)Institut de Chimie des Substances Naturelles, CNRS, ICSN UPR 2301, Université Paris-Saclay, 91198 Gif-sur-Yvette, France. Chemical investigation of the emblematic Catharanthus roseus led to the discovery of trirosaline (1), the first example of a tris-ajmalicine-type monoterpene indole alkaloid and the first natural trimeric MIA ever reported from this deeply dug plant species. Its structure was primarily elucidated based on NMR and HRESIMS analyses, and the nature of its unique intermonomeric linkages was firmly confirmed based on a combination of empirical computation and ML-J-DP4 study. Its absolute configuration was mitigated by comparison of experimental and TDDFT-simulated electronic circular dichroism (ECD) spectra. A possible biosynthetic pathway for trirosaline (1) was postulated. DOI: 10.1021/acs.orglett.3c03972 PMID: 38134219 [Indexed for MEDLINE] 5. J Biochem Mol Toxicol. 2024 Jan;38(1):e23614. doi: 10.1002/jbt.23614. Epub 2023 Dec 8. Ajmalicine induces the pyroptosis of hepatoma cells to exert the antitumor effect. Sun Z(1), Ma C(1), Zhan X(1). Author information: (1)Pharmacy Department, Zhejiang Rongjun Hospital, Jiaxing, Zhejiang Province, China. Ajmalicine (AJM) is an alkaloid extracted from the root of Yunan Rauvolfia verticillata. At present, little research has reported the antitumor pharmacological action and mechanism of AJM. Therefore, this work aimed to conduct relevant research. The mouse hepatoma cell line H22 was intervened with a gradient concentration of AJM. Subsequently, the pyroptosis level was detected by flow cytometry. The expression of inflammatory factors and lactate dehydrogenase was measured by enzyme-linked immunosorbent assay. Reactive oxygen species (ROS) expression was detected by dichlorodihydrofluorescein diacetate probe. In addition, the tumor-bearing model mice were also treated with AJM to analyze tumor growth as well as the expression levels of tissue inflammatory factors and proteins. According to our results, AJM promoted the pyroptosis of H22 cells, increased the pyroptosis rate, and upregulated the expression of inflammatory factors tumor necrosis factor α, interleukin-1β, and interleukin-6. At the same time, it enhanced the openness of membrane pores and increased the expression of ROS. Moreover, AJM promoted the expression of Caspase-3 and N-terminal gasdermin E (GSDME). The AJM-induced pyroptosis was suppressed after N-acetylcysteine treatment to inhibit ROS, while Caspase-3 knockdown also inhibited the AJM-induced pyroptosis. In animals, AJM suppressed tumor growth. AJM can activate ROS to induce pyroptosis and exert the antitumor effect via the noncanonical Caspase-3-GSDME pyroptosis pathway. © 2023 Wiley Periodicals LLC. DOI: 10.1002/jbt.23614 PMID: 38064316 [Indexed for MEDLINE]