Classical analgesic drugs modulate nociceptive-like escape behavior in Drosophila melanogaster larvae

Introduction: Nociceptive stimulus triggers escape responses in Drosophila melanogaster larvae, characterized by 360° rolling behavior along its own body axis. Therefore, it is possible to study analgesic drugs based on this stereo­typical nociceptive-like escape behavior. Here, we aimed to develop...

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Published inResearch results in pharmacology (English ed.) Vol. 8; no. 4; pp. 185 - 196
Main Authors Santos-Silva, Thamyris, Lopes, Caio Fábio Baeta, Gumarães, Jennifer Diniz Soares, Valer, Felipe Berti, Kuhn, Gustavo Campos Silva, Romero, Thiago Roberto Lima, Naves, Lígia Araújo, Duarte, Igor Dimitri Gama
Format Journal Article
LanguageEnglish
Published Belgorod National Research University 22.12.2022
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Summary:Introduction: Nociceptive stimulus triggers escape responses in Drosophila melanogaster larvae, characterized by 360° rolling behavior along its own body axis. Therefore, it is possible to study analgesic drugs based on this stereo­typical nociceptive-like escape behavior. Here, we aimed to develop an analgesic predictive validity test of thermal nociception through D. melanogaster larvae. Materials and methods: We evaluated the effect of classical analgesics (morphine, dipyrone, acetylsalicylic acid (ASA) and dexamethasone (DXM)) in the rolling behavior latency of D. melanogaster larvae exposed to thermal-acute noxious stimulus and nociceptive sensitization paradigm. Drugs were injected into hemocoel (100 nL) before nocicep­tive measurement. Results and discussion: Rolling behavior latency was increased by morphine (2, 4, 8 and 16 ng) in dose-dependent manner. Naloxone (4 ng) fully reversed maximum effect of morphine. Dipyrone (32, 64 and 128 ng) and DXM (8 and 16 ng) elicited dose-dependent antinociceptive effects. Exposure of larvae to 97% of maximal infrared intensity induced nociceptive sensitization, i.e., latency changed from 12 to 7.5 seconds. ASA (25, 50 and 100 ng) and DXM (4, 8 and 16 ng) were administered 150 min after nociceptive sensitization and displayed reverse sensitization in rapid onset (30 min after injection). DXM (16 ng), injected prior to nociceptive sensitization, displayed a delay in the onset of action (150 min after injection). Locomotor behaviors were not affected by analgesic substances. Conclusion: Our findings open perspectives for evaluation and discovery of antinociceptive drugs using D. melano­gaster larvae model. Graphical abstract:
ISSN:2658-381X
2658-381X
DOI:10.3897/rrpharmacology.8.91390