Effects of Cypermethrin on Isolated Frog Sciatic Nerve: An Ultrastructural Study

Aim: Cypermethrin is a potent representative of the type 2 pyrethroid insecticides. This study aimed to investigate the ultrastructural effects of cypermethrin on isolated frog sciatic nerve. Materials and Methods: 28 Rana ridibunda frogs were chosen and randomly divided into four groups (n = 7). After decapitation, sciatic nerves were isolated. All nerves except the control group were exposed to 2.5 µM cypermethrin in Ringer´s solution for 30 (group 1), 45 (group 2) and 60 (group 3) minutes, respectively. Tissue samples were evaluated by transmission electron microscope. Results: Degeneration in the myelin sheath and axon, decrease in the number of microtubules and neurofilaments, and evident damage in mitochondria were observed in all treated groups. Conclusions: Our findings suggest that cypermethrin affects both the myelin sheath and the axon in all groups, thereby impairing the nerve impulse conduction. In addition to these findings, notable degeneration of mitochondria and decrease in numbers of microtubules may also play an important role in this nerve conduction impairment.

Effects of Cypermethrin on Isolated Frog Sciatic Nerve: An Ultrastructural Study

Aim: Cypermethrin is a potent representative of the type 2 pyrethroid insecticides. This study aimed to investigate the ultrastructural effects of cypermethrin on isolated frog sciatic nerve. Materials and Methods: 28 Rana ridibunda frogs were chosen and randomly divided into four groups (n = 7). After decapitation, sciatic nerves were isolated. All nerves except the control group were exposed to 2.5 µM cypermethrin in Ringer´s solution for 30 (group 1), 45 (group 2) and 60 (group 3) minutes, respectively. Tissue samples were evaluated by transmission electron microscope. Results: Degeneration in the myelin sheath and axon, decrease in the number of microtubules and neurofilaments, and evident damage in mitochondria were observed in all treated groups. Conclusions: Our findings suggest that cypermethrin affects both the myelin sheath and the axon in all groups, thereby impairing the nerve impulse conduction. In addition to these findings, notable degeneration of mitochondria and decrease in numbers of microtubules may also play an important role in this nerve conduction impairment.

___

  • Vijverberg HP, de Weille JR. The interaction of pyrethroids with voltage-dependent Na channels. Neurotoxicology 1985; 6: 23-34.
  • Lawrance LJ, Casida JE. Stereospecific action of pyrethroid insecticides on the gamma aminobutyric acid receptor ionophore complex. Science 1983; 221: 1399-401.
  • Bloomquist JR, Adams PM, Soderlund DM. Inhibition of gamma- aminobutyric acid-stimulated chloride flux in mouse brain vesicles by polychloroalkane and pyrethroid insecticides. Neurotoxicology 1996; 7: 11-20.
  • Narahashi T. Cellular and molecular mechanism of action of insecticides: neurophysiological approach. Neurobehav Toxicol Teratol 1982; 4: 753-8.
  • Takahashi M, Le Quesne PM. The effects of pyrethroids deltamethrin and cismethrin on nerve excitability in rats. J Neurol Neurosurg Psychiatry 1982; 45: 1005
  • Husain R, Husain R, Adhami VM, Seth PK. Behavioral, neurochemical, and neuromorphological effects of deltamethrin in adult rats. J Toxicol Environ Health 1996; 48: 515-26.
  • Dick PJ, Shimino M, Schoening GP, Lais AC, Oviat KF, Sparks MF. The evaluation of new synthetic pyrethroid pesticide (permethrin) for neurotoxicity. J Environ Pathol Toxicol Oncol 1984; 5: 109- 17.
  • Cavaliere MJ, Maeda MYS, Shih LWS, Puga FR. Changes in myelinated nerve fibers in skeletal muscle of rats exposed to high doses of permethrin. Ecotoxicol Environ Saf 1990; 3: 139-45.
  • Calore EE, Cavaliere MJ, Puga FR, Calore NM, Rosa AR, Weg R et al. Histologic peripheral nerve changes in rats induced by deltamethrin. Ecotoxicol Environ Saf 2000; 47: 82-6.
  • Greulich K, Pflugmacher S. Uptake and effects on detoxication enzymes of cypermethrin in embryos and tadpoles of amphibians. Arch Environ Con Tox 2004; 47: 489-95.
  • Lajmanovich R, Lorenzatti E, de la Sierra P, Marino F, Stringhini G, Peltzer P. Reduction in the mortality of tadpoles (physalaemus bigillonigerus; cypermethrin in presence of aquatic ferns. Fresen Environ Bull 2003; 12: 1558-61.
  • leptodactylidae) exposed to
  • Khan MZ, Tabassum R, Naqvi SNH, Shah EZ, Tabassum F, Ahmed I, et al. Effect of cypermethrin and permethrin on cholinesterase activity and protein contents in Rana tigrina (amphibia). Turk J Zool 2003; 27: 243-6.
  • Condes-Lara M, Graff-Guerrero A, Vega-Riveroll L. Effects of cypermethrin on the electroencephalographic activity of the rat: a model of chemically induced seizures. Neurotoxicol Teratol 1999; 21: 293-8.
  • Valentine WM. Toxicology of selected pesticides, drugs, and chemicals. Pyrethrin and pyrethroid insecticides. Vet Clin North Am Small Anim Pract 1990; 20: 375-82.
  • Desi I, Dobronyi I, Varga L. Immuno, neuro and general toxicologic animal studies on a synthetic pyrethroid cypermethrin. Ecotoxicol Environ Saf 1986; 12: 220-32.
  • Shakoori AR, Ali SS, Saleem MA. Effects of six months feeding of cypermethrin on the blood and liver of albino rats. J Biochem Toxicol 1988; 3: 59-71.
  • Landon DN, Hall SM. The myelinated nerve fibre, the peripheral nerve. In: Landon DN, editor. The Peripheral Nerve. London: Chapman and Hall, 1976. pp. 1–105.
  • Chiu SY, Ritchie JM, Rogart, RB Stagg D. A quantitative description of membrane currents in rabbit myelinated nerve. J Physiol (Lond) 1979; 292: 149–66.
  • Griffin JW. Pathophysiology of peripheral neuropathies. In: Goldman L, Bennett JC, editors. Cecil Textbook of Medicine, 21st ed. Philadelphia: WB Saunders Co; 2000. p. 2198.
  • Douglas AC, Doyle GG. Toxic responses of the nervous system. In: Amdur MO, Daull J, editors. Casarett and Daull’s Toxicology: The Basic Science of Poisons. New York: McGraw Hill Company Pergamon Press; 1991. p. 421.
  • Brady S, Colman DR, Brophy P. Subcellular organization of the nervous system: Organelles and their function. In: Zigmond MJ, Bloom FE, Landis SC, Roberts JL, Squire LR, editors. Fundamental Neuroscience. San Diego: Academic Press; 1999. p. 87-95.
Turkish Journal of Medical Sciences-Cover
  • ISSN: 1300-0144
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Rapid and simultaneous determination of acetylsalicylic acid, paracetamol, and their degradation and toxic impurity products by HPLC in pharmaceutical dosage forms

İsmail Tuncer DEĞİM, Ahmet AYDIN, Yalçın ÖZKAN, Hüsamettin GÜL, Ahmet SAYAL, Cemal AKAY

The Importance of Serum Procalcitonin Levels in Patients with Chronic Obstructive Pulmonary Disease Exacerbations

Nuri KARADURMUŞ, Kudret EKİZ, Cantürk TAŞÇI, Satılmış İNAL, Arzu BALKAN, Metin ÖZKAN, Hayati BİLGİÇ, Selim KILIÇ

Adhesion of Beta1 Integrin to Fibronectin Regulates CAM-DR Phenotype via p21WAF1/cip1 in HL60 Acute Myeloid Leukemia (AML) Cells

Hande CANPINAR

Prevalence of the Metabolic Syndrome in a Rural Turkish Population: Comparison and Concordance of Two Diagnostic Criteria

Güzel DİŞÇİGİL, Aslıhan KURUL, Ayfer GEMALMAZ, Okay BAŞAK, Serpil AYDIN

Bazı Farmasötik Dozaj Şekillerinde Bulunan Asetil Salisilik Asit, Parasetamol ve Bunların Yıkılma/Katışıklık Ürünlerinin Hızlı ve Eşzamanlı Bir HPLC Yöntemi ile Saptanması

İsmail Tuncer DEĞİM, Ahmet AYDIN, Yalçın ÖZKAN, Hüsamettin GÜL, Ahmet SAYAL, Cemal AKAY

Is Ghrelin a Natural Anti-Microbial Agent?

Süleyman AYDIN

Serum Homocysteine Levels in Highway Toll Collectors and the Relationship with Intima-Media Thickness of the Carotid Artery

Ramazan MEMİŞOĞULLARI

Effects of Cypermethrin on Isolated Frog Sciatic Nerve: An Ultrastructural Study

Ş. Necat YILMAZ, Ülkü ÇÖMELEKOĞLU, Banu COŞKUN, Ebru BALLI, Aynur ÖZGE

Seminal plasma transforming growth factor- B (TGF- B) and epidermal growth factor (EGF) levels in patients with varicocele

Osman ÇAĞLAYAN, Üçler KISA, M. Murad BAŞAR, Mehmet FERHAT

Scalpel Versus Electrocautery Dissections: The Effect on Wound Complications and Pro-Inflammatory Cytokine Levels in Wound Fluid

Mehmet ÖZDOĞAN