EFFECT OF THYMOQUINONE ON GHRELIN EXPRESSION IN RAT STOMACH

Authors

DOI:

https://doi.org/10.71336/jabs.1183

Keywords:

Appetite, ghrelin, stomach, thymoquinone

Abstract

Ghrelin is a polypeptide hormone mainly synthesised from the stomach. Ghrelin also affects carbohydrate metabolism, the gastrointestinal system, the cardiovascular system and cell proliferation. Currently, increasing levels of obesity coupled with sedentary lifestyles have led to increased interest in the study of appetite-controlling factors and herbal agents. One of this plants used for phytotherapy is black cumin (Nigella sativa, N. sativa). Thymoquinone is the principal bioactive component of black cumin seed essential oil. The aim of the present study was to evaluate the possible effects of different doses and routes of administration of thymoquinone on ghrelin expression in the stomach. Thirty-five adult female Sprague Dawley rats were divided into five groups as first group (1 mg/kg thymoquinone, ip), second group (2 mg/kg thymoquinone, ip), third group (10 mg/kg thymoquinone, ip), fourth group (20 mg/kg thymoquinone, gavage), and control group (no treatment) and each group consisted of 7 rats. The histological structure was demonstrated with Crossman's trichrome staining. The presence of ghrelin in stomach sections was demonstrated by using the streptavidin-biotin-complex immunohistochemical method. According to our results, the immunohistochemical reaction in epithelial and glandular cells was weak in all experimental groups compared to the control group. Based on our immunohistochemical findings, it is concluded that thymoquinone treatment in both routes of administration decreases the expression of stomach ghrelin. The observation of immunoreactions of different severity in experimental groups indicate that thymoquinone did not inactivate ghrelin in the stomach, but ghrelin expression varied according to the route of administration and dose.

Author Biography

Şerife Tütüncü

Ondokuz Mayıs Üniversitesi Veteriner Fakültesi Histoloji ve Embriyoloji AD Başkanı, Prof. Dr. 

References

Müller, T. D., Nogueiras, R., Andermann, M. L., Andrews, Z. B., Anker, S. D., Argente, J., Batterham, R. L., Benoit, S., Bowers, C. Y., Broglio, F. (2015): Ghrelin. Molecular metabolism 4(6): 437-460. DOI: https://doi.org/10.1016/j.molmet.2015.03.005

Poher, A. L., Tschöp, M. H., Müller, T. D. (2018): Ghrelin regulation of glucose metabolism. Peptides 100: 236-242. DOI: https://doi.org/10.1016/j.peptides.2017.12.015

Dabak, D. Ö., Kuloğlu, T. (2008): Ghrelin ve metabolik etkileri. Fırat Üniversitesi Doğu Araştırmaları Dergisi 6(3): 105-115.

İlhan, T., Erdost, H. (2009): Ghrelin. Uludağ Üniversitesi Veteriner Fakültesi Dergisi 28(1): 67-74.

Korbonits, M., Goldstone, A. P., Gueorguiev, M., Grossman, A. B. (2004): Ghrelin—a hormone with multiple functions. Frontiers in Neuroendocrinology 25(1): 27-68. DOI: https://doi.org/10.1016/j.yfrne.2004.03.002

Gündoğan, M. (2012): Sleeve gastrektomi rezeksiyon materyallerinde histopatolojik bulgular ile ghrelin ekspresyonu ilişkisi. Pamukkale Üniversitesi Tıp Fakültesi, Denizli, Türkiye.

Öztürk, A. S., Arpacı, A. (2018): Obezite ve Ghrelin/Leptin İlişkisi. Mustafa Kemal Üniversitesi Tıp Dergisi 9(35): 136-151. DOI: https://doi.org/10.17944/mkutfd.328412

Druce, M., Wren, A., Park, A., Milton, J., Patterson, M., Frost, G., Ghatei, M., Small, C., Bloom, S. (2005): Ghrelin increases food intake in obese as well as lean subjects. International Journal of Obesity 29(9): 1130-1136. DOI: https://doi.org/10.1038/sj.ijo.0803001

Wren, A. M., Small, C. J., Abbott, C. R., Dhillo, W. S., Seal, L. J., Cohen, M. A., Batterham, R. L., Taheri, S., Stanley, S. A., Ghatei, M. A., Bloom, S. R. (2001): Ghrelin Causes Hyperphagia and Obesity in Rats. Diabetes 50(11): 2540-2547. DOI: https://doi.org/10.2337/diabetes.50.11.2540

Tutuncu, S. (2020): Black Seed (Nigella Sativa) and Immunomodulatory Effect. International Journal of Veterinary and Animal Research (IJVAR) 3(1): 6-9.

Gözüoğlu, M., Tütüncü, Ş. Timokinonun akciğerler üzerine immünomodülatör etkisi. Veteriner Hekimler Derneği Dergisi 93(2): 105-114. DOI: https://doi.org/10.33188/vetheder.1086458

Datau, E., Surachmanto, E. E., Pandelaki, K., Langi, J. (2010): Efficacy of Nigella sativa on serum free testosterone and metabolic disturbances in central obese male. Acta Medica Indonesiana 42(3): 130-134.

Heshmati, J., Namazi, N., Memarzadeh, M. R., Taghizadeh, M., Kolahdooz, F. (2015): Nigella sativa oil affects glucose metabolism and lipid concentrations in patients with type 2 diabetes: A randomized, double-blind, placebo-controlled trial. Food Research International 70: 87-93. DOI: https://doi.org/10.1016/j.foodres.2015.01.030

Hussain, N., Majid, S., Abbasi, M., Hussain, M., Rehman, K., Khan, M., Dar, M., Shaheen, H., Habib, T. (2017): Use of black seed (Nigella Sativa L.) oil in the management of hypertensive and hyperlipidemic individuals of district Muzaffarabad, Azad Kashmir, Pakistan. Applied Ecology and Environmental Research 15: 31-48. DOI: https://doi.org/10.15666/aeer/1504_031048

Namazi, N., Larijani, B., Ayati, M. H., Abdollahi, M. (2018): The effects of Nigella sativa L. on obesity: A systematic review and meta-analysis. Journal of Ethnopharmacology 219: 173-181. DOI: https://doi.org/10.1016/j.jep.2018.03.001

Safi, S., Razmpoosh, E., Fallahzadeh, H., Mazaheri, M., Abdollahi, N., Nazari, M., Nadjarzadeh, A., Salehi-Abargouei, A. (2021): The effect of Nigella sativa on appetite, anthropometric and body composition indices among overweight and obese women: A crossover, double-blind, placebo-controlled, randomized clinical trial. Complementary Therapies in Medicine 57: 102-653. DOI: https://doi.org/10.1016/j.ctim.2020.102653

Le, P. M., Benhaddou-Andaloussi, A., Elimadi, A., Settaf, A., Cherrah, Y., Haddad, P.S. (2004): The petroleum ether extract of Nigella sativa exerts lipid-lowering and insulin-sensitizing actions in the rat. Journal of Ethnopharmacology 94(2-3): 251-259. DOI: https://doi.org/10.1016/j.jep.2004.04.030

Houcher, Z., Boudiaf, K., Benboubetra, M., Houcher, B. (2007): Effects of methanolic extract and commercial oil of Nigella sativa L. on blood glucose and antioxidant capacity in alloxan-induced diabetic rats. Pteridines 18(1): 8-18. DOI: https://doi.org/10.1515/pteridines.2007.18.1.8

Crossmon, G. (1937): A modification of Mallory’s connective tissue stain with a discussion of the principles involved. The Anatomical Record 69: 33-38. DOI: https://doi.org/10.1002/ar.1090690105

True, L. (1990): Principles of Immunohistochemistry, in Atlas of Diagnostic Immunohistopathology, L. True (ed.), Gower Medical Publishing, New York, ABD.

Rezaie, P., Mazidi, M., Nematy, M. (2015): Ghrelin, food intake, and botanical extracts: A Review. Avicenna journal of phytomedicine 5(4): 271.

Mazidi, M., Taraghdari, S. B., Rezaee, P., Kamgar, M., Jomezadeh, M. R., Hasani, O. A., Soukhtanloo, M., Hosseini, M., Gholamnezhad, Z., Rakhshandeh, H. (2014): The effect of hydroalcoholic extract of Cannabis Sativa on appetite hormone in rat. Journal of Complementary and Integrative Medicine 11(4): 253-257. DOI: https://doi.org/10.1515/jcim-2014-0006

Garcia, A., Otto, B., Reich, S., Weickert, M., Steiniger, J., Machowetz, A., Rudovich, N., Möhlig, M., Katz, N., Speth, M. (2007): Arabinoxylan consumption decreases postprandial serum glucose, serum insulin and plasma total ghrelin response in subjects with impaired glucose tolerance. European Journal of Clinical Nutrition 61(3): 334-341. DOI: https://doi.org/10.1038/sj.ejcn.1602525

Ilhan, T., Erdost, H. (2013): Effects of capsaicin on testis ghrelin expression in mice. Biotechnic & Histochemistry 88(1): 10-18. DOI: https://doi.org/10.3109/10520295.2012.724083

Downloads

Published

2023-05-31

How to Cite

Tütüncü, Şerife, & Delice, N. (2023). EFFECT OF THYMOQUINONE ON GHRELIN EXPRESSION IN RAT STOMACH. Journal of Applied Biological Sciences, 17(2), 257–265. https://doi.org/10.71336/jabs.1183

Issue

Section

Articles

Similar Articles

You may also start an advanced similarity search for this article.