{"id":3288,"date":"2021-10-12T18:17:02","date_gmt":"2021-10-12T15:17:02","guid":{"rendered":"https:\/\/pell.bio\/?p=3288"},"modified":"2022-11-01T15:19:57","modified_gmt":"2022-11-01T12:19:57","slug":"terpene-introduction","status":"publish","type":"post","link":"https:\/\/pell.bio\/en\/terpene-introduction\/","title":{"rendered":"Terpene Introduction"},"content":{"rendered":"\n<p><strong><em>by Vjat\u015belsav \u015auvalov, PELL-s Head Chemist<\/em><\/strong><\/p>\n\n\n\n<p><strong>Introduction<\/strong><\/p>\n\n\n\n<p>According to chemotaxonomy, <em>Cannabis sativa (C. sativa)<\/em> exists in different variants, showing chemical differences, known as chemotypes\/chemovars. Cannabinoid and terpene analysis are used to determine the chemotype\/chemovar of the plant. There are three main types of the plant that are identified by CBD\/THC ratio: <strong>Type I (drug)<\/strong> \u2013 low CBD\/THC ratio (high THC content), <strong>Type II (intermediate) <\/strong>\u2013 CBD\/THC ratio around 0.5 to 3.0, <strong>Ttype III (fibre) \u2013 <\/strong>high CBD\/THC ratio (low THC content, &lt;0,3%). Two additional types include: <strong>Type IV \u2013<\/strong> high CBG content (also contains CBD) and <strong>Type V \u2013<\/strong> undetectable amount of all cannabinoids.<sup> <\/sup><\/p>\n\n\n\n<p><strong>Terpenes<\/strong><\/p>\n\n\n\n<p>Terpenes are produced in the trichomes of the unfertilized female flowering tops (inflorescence of <em>C.&nbsp;sativa<\/em>). <\/p>\n\n\n\n<p>Typically, up to 3-5% of the dry mass of the female inflorescence is comprised of terpenes. The terpenes show very low acute toxicity: typically, acute LD<sub>50<\/sub> values are around 5000 mg\/kg or higher. Because of the very low toxicity, these terpenes are already widely used as food additives and in cosmetic products. Thus, they have been <strong>proven safe<\/strong> <strong>and well-tolerated.<\/strong><\/p>\n\n\n\n<p>Minor botanical chemical compounds, including terpenes, allegedly, contribute to the effect of the main cannabinoids like THC and CBD. The resulting effect is called <strong>herbal synergy<\/strong> or \u201c<strong>the entourage effect<\/strong>\u201d.<\/p>\n\n\n\n<p>While some of the effects of the cannabinoids have been scientifically explained, there is a great deal of uncertainty about the effects of cannabis terpenes in humans beyond fragrance perception. With the possible exception of the sesquiterpene <strong>\u03b2-caryophyllene<\/strong>, no molecular mechanism has been demonstrated to explain the potential synergy of terpenes with cannabinoids.<\/p>\n\n\n\n<p>One potential explanation for the effects connected to terpenes can be found in a recent review, pointing out that the effect is similar to placebo and is partially mediated through the endocannabinoid system, which may explain some of the perceived effects of cannabis products.<\/p>\n\n\n\n<p><strong>Myrcene<\/strong><\/p>\n\n\n\n<p>Most prevalent terpene in modern Cannabis chemotypes (Type II and III). <\/p>\n\n\n\n<p>Present in most cannabis strains and often &#8211; a dominant terpene. It is well established as a flavour ingredient in the food industry and as a fragrance in soap and detergent products. It is also found in lemon grass, bay leaves, ylang-ylang, wild thyme, parsley, cardamom, and basil. Multiple studies demonstrate that it has anti-inflammatory and antioxidant activity.<\/p>\n\n\n\n<p>Controversial evidence says that it is responsible for narcotic-like sedative\/immobilizing action when combined with THC.<\/p>\n\n\n\n<p><strong>Limonene<\/strong><\/p>\n\n\n\n<p>Often \u2013 a dominant terpene in Type I chemotype also found in lemon and other citruses. Studies show that 10mg\/kg\/day of limonene can help in the treatment of neuropathic pain and it was also a sedative at the amount of 5 mg\/kg.<\/p>\n\n\n\n<p>The monoterpene limonene demonstrates significant anti-inflammatory and antioxidant activity both <em>in&nbsp;vitro<\/em> and <em>in vivo<\/em>. Studies show that this terpene is readily absorbed from the digestive tract.<\/p>\n\n\n\n<p><strong>\u03b2-Caryophyllene<\/strong><\/p>\n\n\n\n<p>Present in most cannabis strains and often &#8211; a dominant terpene. <em>In vivo<\/em> study showed caryophyllene has an analgesic and anti-inflammatory activity.<\/p>\n\n\n\n<p>Can bind to cannabinoid receptors and modulate their cell signalling mechanisms. <\/p>\n\n\n\n<p><strong>\u03b1-pinene<\/strong><\/p>\n\n\n\n<p>Found in many <em>C. Sativa<\/em> chemotypes and in other plants. Can be a dominant terpene in some chemotypes. Antioxidant, anti-inflammatory and anti-allergic effects of \u03b1-pinene have been reported in several studies.<\/p>\n\n\n\n<p>Has effects connected to mechanisms related to learning and memory. It is also suggested to reduce the effects of THC overdose.<\/p>\n\n\n\n<p><strong>\u03b1-humulene<\/strong><\/p>\n\n\n\n<p>Present in most cannabis chemotypes and often is a dominant terpene. It is also found in many other plants like hops, sage and ginseng. Traditionally, \u03b1-humulene-containing plants have been used for the treatment of insomnia, depression, nervousness, delirium, anxiety and digestive disorders.<\/p>\n\n\n\n<p><strong>Linalool&nbsp;<\/strong><\/p>\n\n\n\n<p>Found in small amounts in Type I chemotype and Lavender. Has a very distinctive smell. <\/p>\n\n\n\n<p>Studies indicate anti-ischemic, antioxidant and anti-inflammatory effects of the monoterpene linalool. Linalool has also shown a protective effect against liver injury as well as neuroprotective ability.<\/p>\n\n\n\n<p><strong>Bisabolol<\/strong><\/p>\n\n\n\n<p>Present in many cannabis strains and in chamomile. Widely used in the perfume industry. A variety of studies have shown that it has anti-cancer and anti-tumour activities as well as neuroprotective and anti-inflammatory properties.<\/p>\n\n\n\n<p><strong>Terpinolene<\/strong><\/p>\n\n\n\n<p>Often is the main terpene in Type I chemotype. It has been found in a variety of plant sources such as sage, apple, cumin, lilac, tea tree and lemon, but it is primarily isolated from pine and fir trees. Studies show that it has anti-cancer, antioxidant and anti-inflammatory properties.<\/p>\n\n\n\n<p>Which product to choose? \ud83d\udc49 <a href=\"https:\/\/pell.bio\/en\/contact\/\"><span style=\"text-decoration: underline;\">Get in touch with us<\/span><\/a> and we can choose the right product for you together. #pellcare<\/p>\n\n\n\n<p><strong>References<\/strong><\/p>\n\n\n\n<ul class=\"has-small-font-size wp-block-list\"><li>D. Pacifico, Genetics and Marker-assisted Selection of the Chemotype in Cannabis sativa L., (2006), pp. 257-268.<\/li><li>M. A. Lewis, Pharmacological Foundations of Cannabis Chemovars, (2017), pp. 225-233.<\/li><li>T. Nuutinen, Medicinal properties of terpenes found in <em>Cannabis sativa<\/em> and <em>Humulus lupulus<\/em>, (2018), pp. 198-228.<\/li><li>J. K. Booth, Terpenes in Cannabis sativa \u2013 From plant genome to humans, (2019), pp. 67-72.<\/li><li>J. Gertsch, The Intricate Influence of the Placebo Effect on Medical Cannabis and Cannabinoids, (2018), pp. 60\u201364.<\/li><li>E. J. Downer, Anti-inflammatory Potential of Terpenes Present in Cannabis sativa L., (2020), pp. 659-662.<\/li><\/ul>\n","protected":false},"excerpt":{"rendered":"<p>by Vjat\u015belsav \u015auvalov, PELL-s Head Chemist Introduction According to chemotaxonomy, Cannabis sativa (C. sativa) exists in different variants, showing chemical differences, known as chemotypes\/chemovars. Cannabinoid and terpene analysis are used to determine the chemotype\/chemovar of the plant. There are three main types of the plant that are identified by CBD\/THC ratio: Type I (drug) \u2013 [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":3765,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"inline_featured_image":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[81],"tags":[],"class_list":["post-3288","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-cannabis"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Terpene Introduction -<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/pell.bio\/en\/terpene-introduction\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Terpene Introduction -\" \/>\n<meta property=\"og:description\" content=\"by Vjat\u015belsav \u015auvalov, PELL-s Head Chemist Introduction According to chemotaxonomy, Cannabis sativa (C. sativa) exists in different variants, showing chemical differences, known as chemotypes\/chemovars. 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