Trema micranthum

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Trema micranthum
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In Brasília
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Rosales
Family: Cannabaceae
Genus: Trema
Species:
T. micranthum
Binomial name
Trema micranthum
(L.) Blume
Synonyms [1]
List
    • Calyptracordia alba(Jacq.) Britton
    • Cordia alba (Jacq.)Roem. & Schult
    • Gerascanthus albus(Jacq.) Borhidi
    • Lithocardium album(Jacq.) Kuntze
    • Lithocardium albumKuntze
    • Celtis albicansWilld. ex Steud.
    • Celtis canescensKunth
    • Celtis chichileaRuiz & Pav. ex Planch.
    • Celtis curiandiubaM.Gómez ex Planch.
    • Celtis limaLam.
    • Celtis macrophyllaKunth
    • Celtis micrantha(L.) Sw.
    • Celtis microcarpaSalzm. ex Planch.
    • Celtis mollisHumb. & Bonpl. ex Willd.
    • Celtis rufescensBanks ex Planch.
    • Celtis schiedeanaSchltdl.
    • Rhamnus micranthaL. (Basionym)
    • Sponia canescens(Kunth) Decne.
    • Sponia chichileaPlanch.
    • Sponia crassifoliaLiebm.
    • Sponia griseaLiebm.
    • Sponia limaDecne.
    • Sponia macrophylla(Kunth) Decne.
    • Sponia micrantha(L.) Decne. ex Planch.
    • Sponia micrantha(L.) Decne.
    • Sponia mollisDecne.
    • Sponia peruvianaKlotzsch
    • Sponia ripariaDecne.
    • Sponia schiedeana(Schltdl.) Planch.
    • Trema canescens(Kunth) Blume
    • Trema chichilea(Planch.) Blume
    • Trema floridanaBritton ex Small
    • Trema limaBlume
    • Trema macrophylla(Kunth) Blume
    • Trema melinonaBlume
    • Trema micrantha var. obtusatumUrb.
    • Trema micrantha var. strigillosa(Lundell) Standl. & Steyerm.
    • Trema mollis(Humb. & Bonpl. ex Willd.) Blume
    • Trema ripariaBlume
    • Trema rufescensBlume
    • Trema schiedeana(Schltdl.) Blume
    • Trema strigillosaLundell
    • Urtica alnifoliaBertero ex Griseb.

Trema micranthum (sometimes Trema micrantha), the Jamaican nettletree [2] or capulin, [3] is a plant species native to warmer parts of the Western Hemisphere. It has been reported from Mexico, Central America, tropical South America, the Virgin Islands, Jamaica, Cuba, Hispaniola, Puerto Rico, and southern Florida. [1] [4] [5]

Contents

Description

Trema micranthrum is a shrub or small tree up to 10 m (33 ft) tall. Leaves are egg-shaped, up to 9 cm (3.5 in) long, green on top but covered with white, woolly pubescence underneath. Flowers are greenish-white. Fruits are yellow to bright reddish-range, up to 4 mm (0.16 in) in diameter. [4] [6] [7]

Uses

Following the recent local extirpation of slow-growing xalama in San Pablito, Mexico due to unsustainable harvesting driven by tourism, the Otomi people now use T. micranthum bark strips as a raw material for making handmade amate paper. [8]

Phytochemicals

Claims have been made that T. micranthum may contain cannabidiol, [9] a non-psychoactive but medicinally useful component known from Cannabis . However, as with similar claims previously made about the related plant Trema orientale , [10] such claims have not yet been independently replicated by other researchers and are not yet widely accepted by the scientific community. [11] Also, a more recent publication did not provide conclusive evidence, e.g. in the form of fragmentation spectra or the analysis of isolated compounds by NMR. [12]

Related Research Articles

<i>Cannabis</i> Genus of flowering plants

Cannabis is a genus of flowering plants in the family Cannabaceae that is widely accepted as being indigenous to and originating from the continent of Asia. However, the number of species is disputed, with as many as three species being recognized: Cannabis sativa, C. indica, and C. ruderalis. Alternatively, C. ruderalis may be included within C. sativa, or all three may be treated as subspecies of C. sativa, or C. sativa may be accepted as a single undivided species.

<span class="mw-page-title-main">Tetrahydrocannabinol</span> Psychoactive component of cannabis

Tetrahydrocannabinol (THC) is a cannabinoid found in cannabis. It is the principal psychoactive constituent of cannabis and one of at least 113 total cannabinoids identified on the plant. Although the chemical formula for THC (C21H30O2) describes multiple isomers, the term THC usually refers to the delta-9-THC isomer with chemical name (−)-trans9-tetrahydrocannabinol. It is a colorless oil.

<span class="mw-page-title-main">Medical cannabis</span> Cannabis sativa L. (marijuana; hemp) used medicinally

Medical cannabis, medicinal cannabis or medical marijuana (MMJ) refers to cannabis products and cannabinoid molecules that are prescribed by physicians for their patients. The use of cannabis as medicine has a long history, but has not been as rigorously tested as other medicinal plants due to legal and governmental restrictions, resulting in limited clinical research to define the safety and efficacy of using cannabis to treat diseases.

<span class="mw-page-title-main">Cannabinoid</span> Compounds found in cannabis

Cannabinoids are several structural classes of compounds found in the cannabis plant primarily and most animal organisms or as synthetic compounds. The most notable cannabinoid is the phytocannabinoid tetrahydrocannabinol (THC) (delta-9-THC), the primary psychoactive compound in cannabis. Cannabidiol (CBD) is also a major constituent of temperate cannabis plants and a minor constituent in tropical varieties. At least 100 distinct phytocannabinoids have been isolated from cannabis, although only four have been demonstrated to have a biogenetic origin. It was reported in 2020 that phytocannabinoids can be found in other plants such as rhododendron, licorice and liverwort, and earlier in Echinacea.

<i>Trema</i> (plant) Genus of flowering plants belonging to the hop and hemp family

Trema is a genus of about 15 species of evergreen trees closely related to the hackberries (Celtis), occurring in subtropical and tropical regions of southern Asia, northern Australasia, Africa, South and Central America, and parts of North America. They are generally small trees, reaching 10–20 m (33–66 ft) tall.

<span class="mw-page-title-main">Cannabinol</span> Naturally-occurring cannabinoid

Cannabinol (CBN) is a mildly psychoactive phytocannabinoid that acts as a low affinity partial agonist at both CB1 and CB2 receptors. This activity at CB1 and CB2 receptors constitutes interaction of CBN with the endocannabinoid system (ECS).

<span class="mw-page-title-main">Cannabidiol</span> Phytocannabinoid discovered in 1940

Cannabidiol (CBD) is a phytocannabinoid, one of 113 identified cannabinoids in cannabis plants, along with tetrahydrocannabinol (THC), and accounts for up to 40% of the plant's extract. Medically, it is an anticonvulsant used to treat multiple forms of epilepsy. It was discovered in 1940 and, as of 2024 clinical research on CBD included studies related to the treatment of anxiety, addiction, psychosis, movement disorders, and pain, but there is insufficient high-quality evidence that CBD is effective for these conditions. CBD is sold as an herbal dietary supplement and promoted with yet unproven claims of particular therapeutic effects.

<span class="mw-page-title-main">Tetrahydrocannabivarin</span> Homologue of tetrahydrocannabinol

Tetrahydrocannabivarin is a homologue of tetrahydrocannabinol (THC) having a propyl (3-carbon) side chain instead of pentyl (5-carbon), making it non-psychoactive in lower doses. It has been shown to exhibit neuroprotective activity, appetite suppression, glycemic control and reduced side effects compared to THC, making it a potential treatment for management of obesity and diabetes. THCV was studied by Roger Adams as early as 1942.

<span class="mw-page-title-main">Cannabidivarin</span> Group of stereoisomers

Cannabidivarin (CBDV, GWP42006) is a non-intoxicating psychoactive cannabinoid found in Cannabis. It is a homolog (chemistry) of cannabidiol (CBD), with the side-chain shortened by two methylene bridges (CH2 units).

<span class="mw-page-title-main">Cannabigerol</span> Minor cannabinoid

Cannabigerol (CBG) is a non-psychoactive cannabinoid and minor constituent of cannabis. It is one of more than 120 identified cannabinoids found in the plant genus Cannabis. The compound is the decarboxylated form of cannabigerolic acid (CBGA), the parent molecule from which other cannabinoids are biosynthesized.

<i>Cannabis</i> strain Plant varieties of cannabis

Cannabis strains is a popular name to refer to plant varieties of the monospecific genus Cannabis sativa L.. They are either pure or hybrid varieties of the plant, which encompasses various sub-species C. sativa, C. indica, and C. ruderalis.

<span class="mw-page-title-main">Abnormal cannabidiol</span> Synthetic, cannabinoid-like compound

Abnormal cannabidiol (Abn-CBD) is a synthetic regioisomer of cannabidiol, which unlike most other cannabinoids produces vasodilator effects, lowers blood pressure, and induces cell migration, cell proliferation and mitogen-activated protein kinase activation in microglia, but without producing any psychoactive or sedative effects. Abn-CBD can be found as an impurity in synthetic cannabidiol.

<i>Trema orientale</i> Species of tree

Trema orientale is a species of flowering tree in the hemp family, Cannabaceae. It is known by many common names, including charcoal-tree, Indian charcoal-tree, pigeon wood, Oriental trema, and in Hawaii, where it has become naturalized, gunpowder tree, or nalita. It has a near universal distribution in tropical and warm temperate parts of the Old World, with a range extending from South Africa, through the Middle East, the Indian subcontinent and southern China to Southeast Asia and Australia.

The entourage effect is a hypothesis that cannabis compounds other than tetrahydrocannabinol (THC) act synergistically with it to modulate the overall psychoactive effects of the plant.

<span class="mw-page-title-main">Cannabinodiol</span> Chemical compound

Cannabinodiol (CBND), also known as cannabidinodiol, cannabinoid that is present in the plant Cannabis sativa at low concentrations. It is the fully aromatized derivative of cannabidiol (CBD) and can occur as a product of the photochemical conversion of cannabinol (CBN).

<span class="mw-page-title-main">8,9-Dihydrocannabidiol</span> Chemical compound

8,9-Dihydrocannabidiol is a synthetic cannabinoid that is closely related to cannabidiol (CBD) itself. that was first synthesized by Alexander R. Todd in 1940 derived from the catalytic hydrogenation of cannabidiol.

<span class="mw-page-title-main">Cannabidiphorol</span> Chemical compound

Cannabidiphorol, the heptyl-homologue of cannabidiol was identified as a natural phytocannabinoid and named cannabidiphorol (CBDP) in 2019. It had previously been reported as a synthetic compound, but was not identified as a natural product prior to 2019. Recently, CBDP has been gained popularity due to it being synthesized and available on a commercial level.

<span class="mw-page-title-main">Δ-8-Tetrahydrocannabinol</span> Isomer of tetrahydrocannabinol

Δ-8-tetrahydrocannabinol is a psychoactive cannabinoid found in the cannabis plant. It is an isomer of delta-9-tetrahydrocannabinol, the compound commonly known as THC, with which it co-occurs in hemp; natural quantities of ∆8-THC found in hemp are low. Psychoactive effects are similar to that of Δ9-THC, with central effects occurring by binding to cannabinoid receptors found in various regions of the brain.

Cannabinoids are compounds found in the cannabis plant or synthetic compounds that can interact with the endocannabinoid system. The most notable cannabinoid is the phytocannabinoid tetrahydrocannabinol (THC) (Delta-9-THC), the primary intoxicating compound in cannabis. Cannabidiol (CBD) is another major constituent of some cannabis plants. Conversion of CBD to THC can occur when CBD is heated to temperatures between 250–300 °C, potentially leading to its partial transformation into THC.

Conversion of cannabidiol (CBD) to tetrahydrocannabinol (THC) can occur through a ring-closing reaction. This cyclization can be acid-catalyzed or brought about by heating.

References

  1. 1 2 "Trema micranthum (L.) Blume". Plants of the World Online. Royal Botanic Gardens, Kew. Retrieved 10 November 2023.
  2. NRCS. "Trema micratha". PLANTS Database. United States Department of Agriculture (USDA). Retrieved 14 December 2015.
  3. "Trema micrantha". Germplasm Resources Information Network . Agricultural Research Service, United States Department of Agriculture . Retrieved 5 September 2020.
  4. 1 2 "Trema micrantha". Flora of North America @ efloras.org.
  5. "rema micrantha (L.) Blume distribution". Tropicos. Missouri Botanical Garden.
  6. Blume CL (November 1, 1856). Museum botanicum Lugduno-Batavum, sive, Stirpium exoticarum novarum vel minus cognitarum ex vivis aut siccis brevis expositio et descriptio [Botanical Museum of Lyon-Batau, or, a brief exposition and description of new or less known exotic breeds from living or dry] (in Latin). Vol. 2. E.J. Brill.
  7. von Linné C, Salvius L (November 1, 1759). Caroli Linnaei...Systema naturae per regna tria naturae :secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Vol. 2. Impensis Direct. Laurentii Salvii.
  8. Peters CM, Rosenthal J, Urbina T (1987). "Otomi bark paper in Mexico: commercialization of a pre-hispanic technology". Economic Botany. 41 (3): 423–432. doi:10.1007/BF02859061. S2CID   21173713.
  9. Berger JH (4 July 2023). "Medical, but hold the marijuana: new CBD source found in Brazil". phys.org.
  10. Napiroon T, Tanruean K, Poolprasert P, Bacher M, Balslev H, Poopath M, Santimaleeworagun W (2021). "Cannabinoids from inflorescences fractions of Trema orientalis (L.) Blume (Cannabaceae) against human pathogenic bacteria". PeerJ. 9: e11446. doi: 10.7717/peerj.11446 . PMC   8126263 . PMID   34035994.
  11. Appendino G, Taglialatela-Scafati O, Muñoz E (2022). "Cannabidiol (CBD) From Non-Cannabis Plants: Myth or Reality?". Natural Product Communications. 17 (5): 1934578X221098843. doi: 10.1177/1934578X221098843 . S2CID   248734336.
  12. Ribeiro R, da Silva YC, Finotti R, Carneiro GR, Cardoso Dos Santos GR, Pereira HM, Padilha MC, Veiga-Junior VF (2024). "Trema micranthum (L.) Blume as a new source of cannabinoids". Scientific Reports. 14 (1): 29620. doi: 10.1038/s41598-024-80857-6 . PMC   11604998 . PMID   39609538.