Effect of Salicylidene Salicylhydrazide on Testes of Albino Mice: A Histomorphological Study

Authors

  • Sultana Shagufta Department of Anatomy, Khyber Medical College
  • Muhammad Haris Nowshera Medical College
  • Syed Raiq Shah 3Department of Orthodontics, Khyber College of Dentistry
  • Falak Naz Department of Anatomy, Khyber Medical College
  • Zainab Rehman Department of Anatomy, Khyber Medical College
  • Rabail Rabail Department of Anatomy, Nowshera Medical College
  • Sobia Haris Department of Medical Education, Nowshera Medical College
  • Farah Deeba Department of Medical Education, Nowshera Medical College
  • Muhammad Jehangir Khan Department of Pediatric Surgery, Nowshera Medical College

Keywords:

Testicular toxicity evaluation, reproductive toxicity assessment, germinal epithelium, spermatogenesis

Abstract

There is recently an increasing reports of reduction in sperm counts along with other reproductive disorders that is ascribe to the use of drugs and environmental chemicals. In this regard conducting toxicological studies on male reproductive is of paramount importance. This study evaluates salicylidene salicylhydrazide (SCS) for any possible toxicological effects on male reproductive system. Male BALB/c mice were daily administered withSCSat 5, 25, and 50 mg/kg for 7 and 14 days. The body and testes weights were measuredand the testes were subjected to histological tissue processing techniques. The extent of testicular toxicity was evaluated by using modified Johnsen scoring system for assessing the level of spermatogenesis, and morphometric analysis by measuring the diameter of the seminiferous tubules, thickness of germinal epithelium, and area of interstitial cells of Leydig. The body and testes weights showed that the various doses of SCS have no substantial effects after 7 and 14 days. The tested doses of SCS did not produce any distinguishable change in the normal histological features of seminiferous tubules and interstitium after 7 days. However, after 14 days, the 50 mg/kg dose of SCS was associated with vacuolization and loosening of germinal epithelium. These mild-to-moderate histopathological aberrations was confirmed from morphometric analysis in this dose group in which a decrease in the seminiferous tubules diameter and reduction in the thickness of germinal epithelium along with an increase in the interstitial area were observed. These findings concluded that SCS is considered to be relatively safe.

Downloads

Download data is not yet available.

References

Ainscough, E. W., Brodie, A. M., Denny, W. A., Finlay, G. J., Gothe, S. A., & Ranford, J. D. (1999). Cytotoxicity of salicylaldehyde benzoylhydrazone analogs and their transition metal complexes: quantitative structure–activity relationships. Journal of Inorganic Biochemistry, 77(3-4), 125-133.

Akunna, G. G., Obikili, E. N., Anyawu, G. E., & Esom, E. A. (2018). Histochemical and morphometric evidences of the curative role of aqueous zest extract of Citrus sinensis on anti-neoplastic drug-induced testicular degeneration in animal models. Eur. j. anat, 497-507.

Ateşşahin, A., Karahan, İ., Yılmaz, S., Çeribaşı, A. O., & Bulmuş, Ö. (2006). Lycopene prevents adriamycin-induced testicular toxicity in rats. Fertility and sterility, 85, 1216-1222.

Batool, A., & Farzana, F. (2013). Ribavirin exposure induces morphometric changes in the seminiferous tubules of testes in albino rats. Biomedica, 29(4), 256-262.

Bustos-Obregón, E., Del Río, F. C., & Sarabia, L. (2007). Morphometric Analysis of Mice Testicular Tubules after Administration of Malathion and Maca. International Journal of Morphology, 25(2).

Cyr, D. G. (2016). Male Reproductive Toxicology and the Role of Immunohistochemistry. In Technical Aspects of Toxicological Immunohistochemistry (pp. 95-111). Springer, New York, NY.

Coder PS, Sloter ED, Stump DG, Nemec MD, Bowman CJ. (2010). Evaluation of a Male Reproductive Toxicant. In Comprehensive Toxicology (Second Edition). Edited by McQueen CA. Oxford: Elsevier, 61-86

Creasy, D. M. (2002). Histopathology of the male reproductive system I: techniques. Current protocols in toxicology, 12(1), 16-3.

El-Gerbed, M. S. (2013). Histopathological and ultrastructural effects of methyl parathion on rat testis and protection by selenium. Journal of Applied Pharmaceutical Science, 3(8), S53.

González, C. R., González, B., Matzkin, M. E., Muñiz, J. A., Cadet, J. L., Garcia-Rill, E., ... & Bisagno, V. (2015). Psychostimulant-induced testicular toxicity in mice: evidence of cocaine and caffeine effects on the local dopaminergic system. PLoS One, 10(11), e0142713.

Gurel, C., Kuscu, G. C., Buhur, A., Dagdeviren, M., Oltulu, F., Karabay Yavasoglu, N. U., & Yavasoglu, A. (2019). Fluvastatin attenuates doxorubicin-induced testicular toxicity in rats by reducing oxidative stress and regulating the blood–testis barrier via mTOR signaling pathway. Human & experimental toxicology, 38(12), 1329-1343.

Hukkanen, R. R., Halpern, W. G., & Vidal, J. D. (2016). Regulatory Forum Opinion Piece: Review of FDA Draft Guidance Testicular Toxicity—Evaluation during Drug Development Guidance for Industry. Toxicologic pathology, 44(7), 927-930.

Johnson, D. K., Murphy, T. B., Rose, N. J., Goodwin, W. H., & Pickart, L. (1982). Cytotoxic chelators and chelates 1. Inhibition of DNA synthesis in cultured rodent and human cells by aroylhydrazones and by a copper (II) complex of salicylaldehyde benzoyl hydrazone. Inorganica Chimica Acta, 67, 159-165.

Kabel, A. M. (2018). Zinc/alogliptin combination attenuates testicular toxicity induced by doxorubicin in rats: Role of oxidative stress, apoptosis and TGF-β1/NF-κB signaling. Biomedicine & Pharmacotherapy, 97, 439-449.

Kamel, M. E., Mohammad, H. M., Maurice, C., & Hagras, M. M. (2019). Ginseng Nanoparticles Protect Against Methotrexate-Induced Testicular Toxicity in Rats. Egyptian Journal of Basic and Clinical Pharmacology, 9.

Kaur, R., & Kaur, K. (2000). Effects of dietary selenium (SE) on morphology of testis and cauda epididymis in rats. Indian journal of physiology and pharmacology, 44(3), 265-272.

Khorsandi, L., Mirhoseini, M., Mohamadpour, M., Orazizadeh, M., & Khaghani, S. (2013). Effect of curcumin on dexamethasone-induced testicular toxicity in mice. Pharmaceutical biology, 51(2), 206-212.

Kumar, A. R. B. I. N. D., & Susheela, A. K. (1995). Effects of chronic fluoride toxicity on the morphology of ductus epididymis and the maturation of spermatozoa of rabbit. International journal of experimental pathology, 76(1), 1.

Liu, Q., Lei, Z., Huang, A., Lu, Q., Wang, X., Ahmed, S., ... & Yuan, Z. (2017). Mechanisms of the testis toxicity induced by chronic exposure to mequindox. Frontiers in pharmacology, 8, 679.

Mandal, T. K., & Das, N. S. (2010). Testicular toxicity in cannabis extract treated mice: association with oxidative stress and role of antioxidant enzyme systems. Toxicology and industrial health, 26(1), 11-23.

Mustafa, S., Wei, Q., Ennab, W., Lv, Z., Nazar, K., Siyal, F. A., ... & Shi, F. (2019). Resveratrol ameliorates testicular histopathology of mice exposed to restraint stress. Animals, 9(10), 743.

Nna, V. U., Ujah, G. A., Mohamed, M., Etim, K. B., Igba, B. O., Augustine, E. R., & Osim, E. E. (2017). Cadmium chloride–induced testicular toxicity in male wistar rats; prophylactic effect of quercetin, and assessment of testicular recovery following cadmium chloride withdrawal. Biomedicine & Pharmacotherapy, 94, 109-123.

Nna, V. U., Udefa, A. L., Ofutet, E. O., & Osim, E. E. (2017). Testicular and Epididymal Histology of Rats Chronically Administered High Doses of Phosphodiesterase-5 Inhibitors and Tramadol. Niger. J. Physiol. Sci, 32, 55-61.

Osinubi, A. A., Noronha, C. C., & Okanlawon, A. O. (2005). Morphometric and stereological assessment of the effects of long-term administration of quinine on the morphology of rat testis. West African journal of medicine, 24(3), 200-205.

Prihatno, S. A., Padeta, I., Larasati, A. D., Sundari, B., Hidayati, A., Fibrianto, Y. H., & Budipitojo, T. (2018). Effects of secretome on cisplatin-induced testicular dysfunction in rats. Veterinary world, 11(9), 1349.

Rukh, L., Ali, G., Ullah, R., Islam, N. U., & Shahid, M. (2020). Efficacy assessment of salicylidene salicylhydrazide in chemotherapy associated peripheral neuropathy. European Journal of Pharmacology, 888, 173481.

Shahid, M., & Subhan, F. (2014). Comparative histopathology of acetaminophen induced hepatotoxicity in animal models of mice and rats. Pharmacol Online, 3(33), 32-43.

Shahid, M., & Subhan, F. (2014). Protective effect of Bacopa monniera methanol extract against carbon tetrachloride induced hepatotoxicity and nephrotoxicity. Pharmacologyonline, 2(2), 18-28.

Soni, K. K., Zhang, L. T., You, J. H., Lee, S. W., Kim, C. Y., Cui, W. S., ... & Park, J. K. (2015). The effects of MOTILIPERM on cisplatin induced testicular toxicity in Sprague–Dawley rats. Cancer cell international, 15(1), 1-11.

Thompson, S. A., Wheat, L., Brown, N. A., Wingrove, P. B., Pillai, G. V., Whiting, P. J., ... & Wafford, K. A. (2004). Salicylidene salicylhydrazide, a selective inhibitor of β1‐containing GABAA receptors. British journal of pharmacology, 142(1), 97-106.

Published

2021-03-31

How to Cite

Shagufta , S., Haris, M., Raiq Shah, S. ., Naz, F. ., Rehman, Z. ., Rabail, R., Haris, S. ., Deeba, F. ., & Jehangir Khan, M. . (2021). Effect of Salicylidene Salicylhydrazide on Testes of Albino Mice: A Histomorphological Study. European Journal of Volunteering and Community-Based Projects, 1(1), 37-53. Retrieved from https://pkp.odvcasarcobaleno.it/index.php/ejvcbp/article/view/25