Applied Sciences | Open Access | DOI: https://doi.org/10.37547/tajas/Volume08Issue03-06

Rotenone-Induced Dysregulation of Synaptosomal Ca²⁺ And Hypokinetic Behavior in A Rat Model of Parkinsonism

Zayniyeva Makhbuba , Nаtiоnаl Univеrsitу оf Uzbеkistаn named after M. Ulugbek, Tashkent, Almazar 100174, Uzbekistan
Izzatillaeva Sabina , Nаtiоnаl Univеrsitу оf Uzbеkistаn named after M. Ulugbek, Tashkent, Almazar 100174, Uzbekistan
Tajiyeva Oyimjan , Urgench Abu Ali ibn Sina Public Health Technical School, Khorezm, Uzbekistan
Kоzоkоv Islom , Institute of Biophysics and Biochemistry, National University of Uzbekistan, 100174, Tashkent, Uzbekistan
Dеdаbоеv Jobir , Institute of Biophysics and Biochemistry, National University of Uzbekistan, 100174, Tashkent, Uzbekistan
Mukhtоrоv Alisher , Nаtiоnаl Univеrsitу оf Uzbеkistаn named after M. Ulugbek, Tashkent, Almazar 100174, Uzbekistan
Khоshimоv Nozim , Institute of Biophysics and Biochemistry, National University of Uzbekistan, 100174, Tashkent, Uzbekistan

Abstract

Background: Rotenone, a lipophilic mitochondrial complex I inhibitor, is widely used to model Parkinsonian neurodegeneration and synaptic failure.

Objective: To quantify rotenone-associated behavioral changes and determine whether they co-occur with altered glutamate-evoked synaptosomal Ca² dynamics.

Methods: Adult male Wistar rats were randomized into control and rotenone groups (2.5 mg/kg/day, i.p., 11 consecutive days; n=6/group). Exploratory behavior was assessed in an open-field/hole-board ar ena (42 × 42 cm; 42-floor grid; 3 min; ~100 lux). Crude synaptosomes (P2 fraction) were isolated from whole brain tissue, loaded with Fluo4AM (final 5 µM, 30 min, 37°C), and stimulated with Lglutamate (50 µM). Ca² responses were summarized as resting signal, peak amplitude, area under the curve (AUC), and clearance time constant (τ).

Results: Rotenone reduced horizontal locomotion (72±6 vs 14±4 crossings), vertical activity (38±5 vs 8±3 rearings), and holepoking (16±2 vs 6±1; all p<0.05). Synaptosomes from rotenone-treated rats displayed a higher resting Ca²-related fluorescence (+21%) and enhanced glutamate-evoked Ca² responses (peak +18%, AUC +25%), alongside faster decay (τ −17%) relative to controls (p<0.05).

Conclusions: Subchronic rotenone exposure produces a reproducible hypokinetic phenotype that parallels presynaptic Ca² dysregulation, supporting a mechanistic link between mitochondrial stress and abnormal glutamate-triggered Ca² signaling.

Keywords

Parkinsonism, rotenone, synaptosomes

References

Cannon JR, Tapias V, Na HM, Honick AS, Drolet RE, Greenamyre JT. A highly reproducible rotenone model of Parkinson’s disease. Neurobiol Dis. 2009;34(2):279–290. doi:10.1016/j.nbd.2009.01.016.

Fleming SM, Zhu C, Fernagut PO, et al. Behavioral and immunohistochemical effects of chronic intravenous and subcutaneous infusions of varying doses of rotenone. Exp Neurol. 2004;187(2):418–429. doi:10.1016/j.expneurol.2004.01.023.

Betarbet R, Sherer TB, MacKenzie G, Garcia‑Osuna M, Panov AV, Greenamyre JT. Chronic systemic pesticide exposure reproduces features of Parkinson’s disease. Nat Neurosci. 2000;3(12):1301–1306. doi:10.1038/81834.

Hardingham GE, Bading H. Synaptic versus extrasynaptic NMDA receptor signalling: implications for neurodegenerative disorders. Nat Rev Neurosci. 2010;11(10):682–696. doi:10.1038/nrn2918.

Paoletti P, Bellone C, Zhou Q. NMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease. Nat Rev Neurosci. 2013;14(6):383–400. doi:10.1038/nrn3504.

Carter RJ, Lione LA, Humby T, et al. Characterization of progressive motor deficits in mice transgenic for the human Huntington’s disease mutation. Curr Protoc Neurosci. 2001;Chapter 9:Unit 9.5.

Johnson ME, Bobrovskaya L. An update on the rotenone models of Parkinson’s disease: their ability to reproduce the features of clinical disease and model gene–environment interactions. Neurotoxicology. 2015;46:101–116. doi:10.1016/j.neuro.2014.12.002.

Surmeier DJ, Obeso JA, Halliday GM. Selective neuronal vulnerability in Parkinson disease. Nat Rev Neurosci. 2017;18:101–113. doi:10.1038/nrn.2016.178.

Nicholls DG. Mitochondria and neuronal survival. Physiol Rev. 2000;80(1):315–360. doi:10.1152/physrev.2000.80.1.315.

Prut L, Belzung C. The open field as a paradigm to measure the effects of drugs on anxiety-like behaviors: a review. Eur J Pharmacol. 2003;463(1–3):3–33. doi:10.1016/S0014-2999(03)01272-X.

Paredes RM, Etzler JC, Watts LT, Zheng W, Lechleiter JD. Chemical calcium indicators. Methods. 2008;46(3):143‑151. doi:10.1016/j.ymeth.2008.09.025.

Gee KR, Brown KA, Chen WN, Bishop‑Stewart J, Gray D, Johnson I. Chemical and physiological characterization of fluo‑4 Ca²⁺‑indicator dyes. Cell Calcium. 2000;27(2):97‑106. doi:10.1054/ceca.1999.0095.

Grynkiewicz G, Poenie M, Tsien RY. A new generation of Ca²⁺ indicators with greatly improved fluorescence properties. J Biol Chem. 1985;260(6):3440‑3450.

Petrischev N.N., Vasina L.V., Seliutin A.V., Chepanov S.V., Selkov S.A. The application of Fluo-3 AM in measurement of level of cytoplasmic calcium in thrombocytes by flow cytofluorometry. // Klinicheskaya Laboratornaya Diagnostika (Russian Clinical Laboratory Diagnostics) – 2017. – V.62, №2. – P. 97-99.

Weiler MH, Gundersen CB, Jenden DJ. Choline uptake and acetylcholine synthesis in synaptosomes: investigations using two different labeled variants of choline. J Neurochem. 1981 May;36(5):1802-12. doi: 10.1111/j.1471-4159.1981.tb00434.x.

Numonjonovich, K. N. ., Baxtiyarovich, K. I. ., Ugli, D. J. I. ., Salimovich, K. S. ., Ugli, M. A. A. ., Ugli, O. M. M. ., Erkinovich, N. K. ., Amindjanovna, M. Z. ., Abdullayevna, S. G. ., & Nurillayevich, R. R. . (2024). Еffесt of Pоlyphеnоls on Сhаngеs in thе Hеmоstаtiс Systеm of Blооd Plаsmа in Hеаlthy and Mоdеl Rаts with Аlzhеimеr’s Disеаsе. Trends in Sciences, 21(9), 8081. https://doi.org/10.48048/tis.2024.8081

Nozim N. Khoshimov, Alisher A. Mukhtorov, Kabil E. Nasirov, Rakhmatilla N. Rakhimov, Rahmatjon R. Mamadaminov. Effects of Polyphenols on changes in the transport of Ca2+ NMDA-receptors under the influence of L-glutamate. Research Journal of Pharmacy and Technology 2023; 16(3):1205-3. doi: 10.52711/0974-360X.2023.00200.

Ugli, D. J. I., Bakhtiyarovich, K. I., Numonjonovich, K. N., Erkinovich, N. K. ., Madmuradovna, R.G., Abdugaparovich, M. A., Amindjanovna, M. Z., Irkinovna, Y. R., Rasuldjanovich, M. R., & Raxmankulovna, A. N. (2025). The Influence of Polyphenols on Calcium Dynamics in Synaptosomes of Model Rats with Attention Deficit Hyperactivity Disorder of Varying Ages. Trends in Sciences, 22(9), 10434. https://doi.org/10.48048/tis.2025.10434

Nozim N. Khoshimov, Alisher A. Mukhtorov, Kabil E. Nasirov, Rakhmatillo N. Rakhimov, & Rahmatjon R. Mamadaminov. Effeсts of Рolyрhenols on Сhanges in the Transрort of Сa2+ NMDA-reсeрtors Under the Influenсe of L-glutamate against the Baсkground of Alzheimer’s Disease. Journal of Рharmaceutical Negative Results, 2022. 1322–1332.

Khoshimov, N. N., Rahimova, G. L., Mirzakulov, S. O., Azizov, V. G., Abduboqiyev, A. R., & Rakhimov, R. N. (2021). Study of the Neuroprotective Properties of Biologically Active Compounds. Annals of the Romanian Society for Cell Biology, 25(6), 2775-2782.

Khoshimov, N. N., & Nasirov, K. E. (2017). Action of Cytisinum on the Transport Mediators and Calcium Channel of Glutamatergic Neurotransmitter Systems of the NMDA Receptor. European Journal of Medicine, (5-2), 56-63.

Khoshimov, N. N., Raimova, G. M., Nasirov, K. E., Rakhimov, R. N., & Azizov, V. G. (2020). The Effect of Sp-6 On The Transport of Mediators of NMDA-Receptors and Ca 2+-channels in Synaptosomes of rat brain. European Journal of Molecular & Clinical Medicine, 7(3), 2435-2446.

Khoshimov, N. N., Kabil, N. E., & Eshbakova, K. A. (2015). Research influence biological active agents in the course of regulation of functional activity of platelets and system of a haemostasis. European Journal of Medicine, 2, 88-93.

Khoshimov, N. N., Mukhtorov, A. A., Nasirov, K. E., Rakhimov, R. N., & Mamadaminov, R. R. (2022). Effeсts of Рolyрhenols on Сhanges in the Transрort of Сa2+ NMDA-reсeрtors Under the Influenсe of L-glutamate against the Baсkground of Alzheimer’s Disease. Journal of Рharmaceutical Negative Results, 13, 1322-1332.

Khoshimov, N. N., Nasirov, K. E., Raimova, G. M., Musaeva, M. K., Azizov, V. G., Тuraev AS, M. S., ... & Abdusalоmоv Sh, A. (2021). Study of the effect of polysaccharides on hemostasis. The American journal of medical sciences and pharmaceutical research, 3(01), 131-138.

Khoshimov, N. N., Saidmurodov, S. A., & Rakhimov, R. N. (2021). The Mechanism of action of polyphenol on changes in the dynamics of calcium in the synaptosomes of the rat brain against the background of glutamate. The American journal of applied sciences, 3 (03), 48-55.

Mukhtorov, A. A., Mamadaminov, R. R., Khoshimov, N. N., Nasirov, K. E., Rakhimov, R. N., & Gaybullo, L. X. (2022). Regulation of transport of Ca2+ NMDA-receptors in rat brain synaptosomes under the influence of polyphenols. European Journal of Medicine, 10(1), 3-11.

Download and View Statistics

Views: 0   |   Downloads: 0

Copyright License

Download Citations

How to Cite

Zayniyeva Makhbuba, Izzatillaeva Sabina, Tajiyeva Oyimjan, Kоzоkоv Islom, Dеdаbоеv Jobir, Mukhtоrоv Alisher, & Khоshimоv Nozim. (2026). Rotenone-Induced Dysregulation of Synaptosomal Ca²⁺ And Hypokinetic Behavior in A Rat Model of Parkinsonism. The American Journal of Applied Sciences, 8(3), 58–63. https://doi.org/10.37547/tajas/Volume08Issue03-06