Poppy plants have become widely recognized in Canada as a symbol for Remembrance Day and were the inspiration for the poem, in Flanders fields. However, poppies also have medicinal uses that continue to be used to this day, a drug used as a pain killer – morphine. Morphine while used medicinally, has constant abusive use along with other opioids for an average of 15 deaths per day from April 2025 to May 2026 (Government of Canada 2025).
However, a pain reliever was not the intended purpose poppy plants had when they began synthesizing morphine. This initial purpose was a defense mechanism for the plants when they were damaged.
A study was done in 2001 testing the effects of damage on poppy capsules vs. no damage done to the capsules (Morimoto et al. 2001). In response to induced stress, the damaged capsules metabolized morphine into bismorphine that consists of two morphine groups that cluster along the plant cell wall. Bismorphine primarily binds to pectin, which acts like a structural glue that keeps the cell walls bound together (Braidwood et al. 2014). This binding of bismorphine to pectin further leads to a resistance of pectinases which are a group of enzymes that break down pectin and promote the degradation of the cell wall (Dong et al. 2024). The presence of these compounds when there is damage to the cell overall enables poppy plants to induce their defense system (Morimoto et al. 2001). A high-performance liquid chromatography (HPLC) method was used to identify bimorphine quantities in damaged and non-damaged capsules in figure 1.

Morphine while being used as a defense for plants is also very addictive once patients require constant consumption of the opioid. Once morphine enters the body, it binds to the opioid receptors within the brain such as the mu receptor. These receptors are a group of G-protein coupled receptors and cause significant molecular changes within the cell. For example, it activates the release of potassium channels, reduces calcium conductance, and inhibits adenylate cyclase activity (Listos et al. 2019)(Figure 2). Adenylate cyclase is an enzyme that is responsible for converting adenosine triphosphate (ATP) into cyclic adenosine monophosphate (cAMP). cAMP is a secondary messenger that is used in several pathways within a cell and executes precise cellular actions (Franziska 2025). By lowering the levels of cAMP within the neuron, it decreases the neurotransmission causing drowsiness, slow respiration, and overall pain relief (Kosten and George 2002).

Morphine can be extremely addictive caused by the irregular release of dopamine when the molecule is bound to the mu receptors. Inhibitory neurons are linked to cells that release dopamine but have mu receptors on them. When morphine binds to the receptors, it “takes off the breaks” of the cell that produces dopamine, flooding the brain with mood enhancing neurotransmissions (Goldsmith 2024).
While the intended purposes of morphine are to be a repair agent for plants and to aid patients when dealing with the aftermath of painful procedures, the side effects of addiction should be considered before it is prescribed without a second thought.
References
Braidwood, L., C. Breuer, and K. Sugimoto. 2014. “My Body Is a Cage: Mechanisms and Modulation of Plant Cell Growth.” New Phytol 201: 388–402. https://doi.org/10.1111/nph.12473.
Dong, Yuhe, Tao Jiang, and Tong Wu. 2024. “Enzyme-Responsive Controlled-Release Materials for Food Preservation and Crop Protection – a Review.” International Journal of Biological Macromolecules 254 (January): 128051. https://doi.org/https://doi.org/10.1016/j.ijbiomac.2023.128051.
Franziska. 2025. “cAMP – a Currency of Cell Signaling – Biocrates Life Sciences Gmbh.” Biocrates Life Sciences Gmbh, October 14. https://biocrates.com/camp/.
Goldsmith, Sarah. 2024. “Hooked on a Feeling: Opioids Evoke Positive Feelings Through a Newly Identified Brain Region | MUSC Health.” Muschealth.Org. https://muschealth.org/content-hub/News/2024/08/09/opioid-addiction.
Government of Canada. 2025. “Opioid- and Stimulant-Related Harms in Canada.” Health Infobase, Government of Canada, March 7. https://health-infobase.canada.ca/substance-related-harms/opioids-stimulants/.
Kosten, Thomas, and Tony George. 2002. “The Neurobiology of Opioid Dependence: Implications for Treatment.” Science & Practice Perspectives 1 (1): 13–20. https://doi.org/10.1151/spp021113.
Listos, Joanna, Małgorzata Łupina, Sylwia Talarek, Antonina Mazur, Jolanta Orzelska-Górka, and Jolanta Kotlińska. 2019. “The Mechanisms Involved in Morphine Addiction: An Overview.” International Journal of Molecular Sciences 20 (17): 4302. https://doi.org/10.3390/ijms20174302.
Matthews, Simon. 2021. Oral Morphine Patient Information University Hospitals Sussex NHS Foundation Trust. https://www.uhsussex.nhs.uk/wp-content/uploads/2022/09/Oral-morphine.pdf.
Morimoto, Satoshi, Kazunari Suemori, Jun Moriwaki, et al. 2001. “Morphine Metabolism in the Opium Poppy and Its Possible Physiological Function: BIOCHEMICAL CHARACTERIZATION of the MORPHINE METABOLITE, BISMORPHINE *.” Journal of Biological Chemistry 276 (41): 38179–84. https://doi.org/10.1074/jbc.M107105200.
Odegaard, Katherine E., “In utero and Postnatal Oxycodone Exposure: Implications for Intergenerational Effects” (2021). Theses & Dissertations. 518.
https://digitalcommons.unmc.edu/etd/518
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