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Seizures negatively impact various functions and life quality. Planaria worms were exposed to varying concentrations of chemoconvulsants to evaluate their seizure phenotypes and disruptive motility. This study proposes using planaria worms as a model for acute seizures in humans and holds significance in drug development for epilepsy.
Epilepsy is among the most prevalent neurological disorders characterized by recurring spontaneous seizures. Seizures represent a clinical manifestation of uncontrolled, excessively synchronized neural cell activity. The extent of brain damage from seizures depends on their duration and intensity. Regrettably, there is no effective remedy for epilepsy. The aim of this investigation is to assess whether the planaria worm Dugesia dorotocephala could serve as a model to aid in identifying and developing treatments for epilepsy that can target acute seizures. Currently, various models, such as marine models, are used to evaluate antiseizure medications (ASM). However, they are very expensive, and there are ethical concerns. Alternatively, invertebrate models offer a cost-effective research opportunity in the drug discovery process for ASM. Planaria belong to the flatworm family and inhabit marine freshwater and terrestrial environments. Dugesia dorotocephala is the dominant species of aquatic planaria across North America. D. dorotocephala presents as a viable invertebrate model for epilepsy studies due to its cost-effectiveness, vertebrate-like neurons, and quantifiable behaviors, unlike other invertebrates or larger animals. They have been used in various pharmacology and environmental toxicology studies related to age, memory, and regeneration. In this study, planaria were exposed to different concentrations of pilocarpine, a common chemoconvulsant to study their behavior upon exposure. Following the observation, planaria were euthanized and preserved in either formaldehyde or Golgi solution for neurohistological assessment. Six distinct behavioral phenotypes were observed in planaria: dorsal oscillations, head oscillations, tail dorsal expansion, C-shape, head flick, and tail flick. Dorsal oscillation frequencies were significantly increased among experimental groups compared to the control and exhibited dose dependence. Additionally, pilocarpine disrupted the motility of the planaria. Pilocarpine-induced seizures in planaria can serve as a model to evaluate acute seizures and antiseizure medication, which is essential in developing therapeutic interventions for human patients suffering from epilepsy.
Epilepsy, characterized by two or more seizures within 24 h without an apparent cause, impacts ~50 million people globally1. Among them, 10-15 million individuals are reported to have drug-resistant epilepsy2. Therefore, epilepsy drug investigation is crucial. The condition entails brief episodes of either partial or generalized involuntary movement, ranging from blank staring to body stiffening and shaking, and is linked with a surge of electrical activity in the brain3.
Historically, epilepsy research has relied on rodents and other mammals due to their evolutionary s....
NOTE: The overall experimental design is described in Figure 1.
1. Behavior phenotype assay
The following behavior was observed by the planaria exposed to varying concentrations of pilocarpine:
Dorsal oscillations: a bubble-like formation that travels from the cranial end of the planarian's body to the caudal end.
Head oscillations: bubble-like formation by the head of the planarian that forms a tadpole-like appearance.
C-Shape: head moving clockwise and tail moving counterclockwise to form a C.
Head flick: the head of the planarian abruptly jerks to the left or the right.
Tail.......
This study demonstrated pilocarpine-induced behavior in planaria at different concentrations. The most pertinent behavior was oscillating dorsal expansion, as this behavior has not been documented in other studies regarding seizure-like behavior in planaria9,10,11,12. The mechanism by which pilocarpine induces seizure-like behaviors in planaria is still unknown. However, this study demonstrates.......
The authors have nothing to declare.
We want to thank EVMS Research Incentive Fund (PI: A.E. Musto) and Dr. Jorge Jacot for his helpful suggestions with optimizing the immunofluorescence protocol.
....Name | Company | Catalog Number | Comments |
1.5 mL centrifuge tubes | |||
4% paraformaldehyde solution | Himedia | TCL119 | |
Aqueous mounting media | Clini Sciences | NB-47-02240-30ML | |
Beakers (one for each concentration tested) | |||
Carolina Springwater | carolina | 132450 | |
Cryostat | |||
Diluted primary and secondary antibodies | |||
Ethanol (100%) | sigma Aldrich | ||
EthosVision XT 16 | noldus | ||
Fiji Version 2.9.0 | |||
Gelatin-coated slides | sigma Aldrich | 643203 | |
Golgi Antibody 1H6 | DSHB | AB_2619608 | |
Golgi stain kit_ | Neuroscience Associate | PK 401/401A | |
Hydrogen Peroxide | |||
Methanol | |||
Mounting media | thermo fischer scientific | ||
OCT compound | |||
PBS buffer | sigma Aldrich | P4417 | |
Powdered Milk | |||
Tin foil | |||
Transfer pipettes | |||
Xylene |
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