The Effects of Caffeine and Alcohol on the Electrically Evoked Responses of L. terrestris
Journal of Basic and Applied Research International, Volume 29, Issue 3,
Page 16-27
DOI:
10.56557/jobari/2023/v29i38369
Abstract
Regulation on animal research, largely focused on vertebrates, has led to greater expenses for researchers and institutions. Invertebrate animals, however, are rarely included in regulatory oversight, making experimentation comparatively more flexible and inexpensive. Yet, invertebrates are largely overlooked in neurophysiological research, even though the simplicity of invertebrate nervous system models has its advantages. While somatosensory, visual, and auditory evoked potential may be used for pharmacological and toxicological assessment of drugs in both animals and humans, only minor research carried out on invertebrates generally due to the disregard upon comparison between physiological phases or chromosomes of both invertebrates and humans. This study aims to analyze the viability of Lumbricus terrestris, or the common earthworm, as a potential model for electrical somatosensory evoked potential propagation and for drug safety pharmacology assessment. Varying intensities of electrical stimulation potential from 45 ~ 137 mV and accumulative substance injections up to 300 ul were to be used to evaluate telemetric-recorded changes in the evoked potential of the earthworm, and to track the extent of its reproducibility. Alcohol and caffeine, as they are two of the most commonly consumed chemicals in beverages among adolescents, and much was already known about their neurological effects, making the earthworm model’s response to foreign substances evaluable. Numerical changes in latent period, peak point, trough point and wave width of the evoked potential elicited by each substance were analyzed using regression analysis. We found that our peak point and wave width evoked potential parameters were highly indicative of the earthworm’s capability as an evoked potential invertebrate model, especially because responses exhibited expected outcomes of the excitable and inhibitory effects of caffeine and alcohol with high reproducibility.
- Alcohol
- caffeine
- earthworm
- electrically evoked responses
- stimulation and responses
How to Cite
References
National Research Council (US) Committee to Update Science, Medicine, and Animals. Science, Medicine, and Animals. Washington (DC): National Academies Press (US). Regulation of Animal Research; 2004.
Available:https://www.ncbi.nlm.nih.gov/books/NBK24650/
Thulin JD, Bradfield JF, Bergdall VK, Conour LA, Grady AW, Hickman DL, Norton JN, Wallace JM. The cost of self-imposed regulatory burden in animal research. FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology. 2014;28(8):3297–3300. Available:https://doi.org/10.1096/fj.14-254094
Wilson-Sanders SE. Invertebrate models for biomedical research, testing, and education. ILAR journal. 2011;52(2):126–152. Available:https://doi.org/10.1093/ilar.52.2.126
Horvath K, Angeletti D, Nascetti G, Carere C. Invertebrate welfare: an overlooked issue. Annali dell'Istituto superiore di sanita. 2013;49(1):9–17. Available:https://doi.org/10.4415/ANN_13_01_04
Fründ, Heinz-Christian & Butt, Kevin & Capowiez, Yvan & Eisenhauer, Nico & Emmerling, Christoph & Ernst, Gregor & Potthoff, Martin & Schädler, Martin & Schrader, Stefan. Using earthworms as model organisms in the laboratory: Recommendations for experimental implementations. Pedobiologia. 2010;53: 119-125.
DOI:10.1016/j.pedobi.2009.07.002
Roots BI, Lane NJ. Myelinating glia of earthworm giant axons: Thermally induced intramembranous changes. Tissue & cell, 1983;15(5):695–709. Available:https://doi.org/10.1016/0040-8166(83)90044-7
Baker A, Widrich J. Somatosensory EPs. [Updated 2022 Aug 22]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan-. Available:https://www.ncbi.nlm.nih.gov/books/NBK544358/
Kiszler G, Varhalmi E, Berta G, Molnar L. Organization of the sensory system of the earthworm Lumbricus terrestris (Annelida, Clitellata) visualized by DiI. Journal of morphology. 2012;273(7):737–745.
Available:https://doi.org/10.1002/jmor.20018
Arezzo JC, Simson R, Brennan NE. EPs in the assessment of neurotoxicity in humans. Neurobehavioral toxicology and teratology. 1985;7(4):299–304.
Dyer RS. The use of sensory EPs in toxicology. Fundamental and applied toxicology : official journal of the Society of Toxicology. 1985;5(1):24–40.
Ferré S, O'Brien MC. Alcohol and caffeine: The Perfect Storm. Journal of Caffeine Research. 2011;1(3):153–162.
Available:https://doi.org/10.1089/jcr.2011.0017
Karl E. Misulis, Toufic Fakhoury. Spehlmann's Evoked Potential Primer. Butterworth-heinemann; 2001.
Husain AM. (n.d.). 1: Basics of EPs. In Illustrated Manual of Clinical Evoked Potentials.
Available:https://doi.org/10.1891/9781617050107.0001
Mark Banoub, John E, Tetzlaff, Armin Schubert. Pharmacologic and Physiologic Influences Affecting Sensory EPs: Implications for Perioperative Monitoring. Anesthesiology. 2003; 99:716–737 DOI:https://doi.org/10.1097/00000542-200309000-00029
-
Abstract View: 0 times
PDF Download: 0 times