Therapeutic effects of aqueous extract of aerial parts of Teucrium polium L. against acrylamide-induced thyro-reprotoxicity in male rats
DOI:
https://doi.org/10.55779/nsb17212522Keywords:
acrylamide; histopathology study; Jaada; repro-hormones; sperm parameters; testis; thyroid glandAbstract
Acrylamide (ACR) is a toxic chemical found in food and the environment. Medicinal traditional plants are used as alternatives to attenuate the adverse effects of many hazardous chemicals on human health. This study investigated the protective effects of prepared traditional aqueous extract of aerial parts of Teucrium polium L. (T. polium) on ACR-induced thyro-reprotoxicityin male rats. In this study, 24 rats were distributed into four equal groups and treated orally for 21 days. The first group was the control; the second and third groups received ACR (20 mg/kg/bw) and T. polium (400 mg/kg/bw), respectively; and the fourth group received T. polium and ACR. ACR caused a significant decrease in daily body weight and no changes in testes and epididymis relative weights. Compared to controls, ACR triggered hypothyroidism, as shown by a significant decrease in triiodothyronine and thyroxine plasma levels and thyroid histopathology. Most of thyroid follicles were hypertrophied; other follicles degenerated, and their form changed with the absence of colloid and fusion of the follicles, while others appeared with multiple layers that obliterated the lumen, and others were infiltrated by inflammatory cells. Moreover, ACR caused atrophy and severe degeneration in both seminiferous and epididymal tubules. The majority of these tubules were empty and devoid of spermatozoa. ACR also significantly decreased testosterone levels, sperm concentration, motility, and vitality. However, all deleterious effects of ACR were ameliorated following the administration of T. polium. The aerial parts of aqueous extract of T. polium provide substantial protection against ACR-induced thyro-reprotoxicity, thus improving male fertility and reproduction.
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Abd-Elsalam RM, El Badawy SA, Ogaly HA, Ibrahim FM, Farag OM, Ahmed KA (2021). Eruca sativa seed extract modulates oxidative stress and apoptosis and up-regulates the expression of Bcl-2 and Bax genes in acrylamide-induced testicular dysfunction in rats. Environmental Science and Pollution Research 28(38):53249-53266. https://doi.org/10.1007/s11356-021-14532-y
Abdolghaffari AH, Baghaei A, Moayer F, Esmaily H, Baeeri M, Monsef-Esfahani HR, ... Abdollahi M (2010). On the benefit of Teucrium in murine colitis through improvement of toxic inflammatory mediators. Human and Experimental Toxicology 29(4):287-295. https://doi.org/10.1177/0960327110361754
Abdulkareem SM, Nanakali NM (2019). Quercetin reduces oxidative stress damage to reproductive profile induced by 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin in male albino rats (Rattus norvegicus L.). Applied Ecology and Environmental Research 17(6). http://dx.doi.org/10.15666/aeer/1706_1318513197
Ajibare AJ, Odetayo AF, Akintoye OO, Olayaki LA (2024). Zinc ameliorates acrylamide-induced oxidative stress and apoptosis in testicular cells via Nrf2/HO-1/NfkB and Bax/Bcl2 signaling pathway. Redox Report 29(1):2341537. https://doi.org/10.1080/13510002.2024.2341537
Alabbadi RA, Ayaz NO, Elhalwagy MEA (2022). Attenuating effect of Chlorella Vulgaris against acrylamide intoxication on thyroid gland. International Journal of Health Sciences 6(S10):962–975. https://doi.org/10.53730/ijhs.v6nS10.13749
Algefare A, Sedky AM, Alfwuaires M (2021). Apigenin ameliorates lead acetate induced hyperlipidemia, hypothyroidism and hypogonadism in male rats. https://doi.org/10.21203/rs.3.rs-600247/v1
Alhealy E, Alqazzaz M, Wahda AN (2021). Impact of selenium on structural changes induced by hypothyroidism in adult male rat׳ s testis. Iraqi Journal of Pharmacy 18(1):20-32.
Amer NA, Ibrahim NM, Ibrahim BA, Agaga RA (2025). Histological and biochemical analysis of the possible protective effects of luteolin on testicular injury caused by Lead acetate in adult male albino rats. Mansoura Journal of Forensic Medicine and Clinical Toxicology 33(1):13-32. https://doi.org/10.21608/mjfmct.2024.309523.1084
Atrahimovich D, Avni D, Khatib S (2021). Flavonoids-macromolecules interactions in human diseases with focus on Alzheimer, atherosclerosis and cancer. Antioxidants 10(3):423. https://doi.org/10.3390/antiox10030423
Badr GM, Elsawy H, Sedky A, Eid R, Ali A, Abdallah BM, ... Abdel-Moneim AM (2019). Protective effects of quercetin supplementation against short-term toxicity of cadmium-induced hematological impairment, hypothyroidism, and testicular disturbances in albino rats. Environmental Science and Pollution Research 26:8202-8211. https://doi.org/10.1007/s11356-019-04276-1
Bahramikia S, Gavyar PHH, Yazdanparast R (2022). Teucrium polium L: An updated review of phytochemicals and biological activities. Avicenna Journal of Phytomedicine 12(3):224. https://dx.doi.org/10.22038/ AJP.2021.19155
Bahramikia S, Yazdanparast R (2012). Phytochemistry and medicinal properties of Teucrium polium L. (Lamiaceae). Phytotherapy Research 26(11):1581-1593. https://doi.org/10.1002/ptr.4617
Benchikha N, Messaoudi M, Larkem I, Ouakouak H, Rebiai A, Boubekeur S, ... Youssef FS (2022). Evaluation of possible antioxidant, anti-hyperglycaemic, anti-Alzheimer and anti-inflammatory effects of Teucrium polium aerial parts (Lamiaceae). Life 12(10):1579. https://doi.org/10.3390/life12101579
Bin-Jumah MN, Al-Huqail AA, Abdelnaeim N, Kamel M, Fouda MM, Abulmeaty M M, ... Abdel-Daim MM (2021). Potential protective effects of Spirulina platensis on liver, kidney, and brain acrylamide toxicity in rats. Environmental Science and Pollution Research 28:26653-26663. https://doi.org/10.1007/s11356-021-12422-x
Boudjelal A, Henchiri C, Sari M, Sarri D, Hendel N, Benkhaled A, Ruberto G (2013). Herbalists and wild medicinal plants in M'Sila (North Algeria): An ethnopharmacology survey. Journal of Ethnopharmacology 148(2):395-402. http://dx.doi.org/10.1016/j.jep.2013.03.082
Chabane S, Boudjelal A, Keller M, Doubakh S, Potterat O (2021). Teucrium polium-wound healing potential, toxicity and polyphenolic profile. South African Journal of Botany 137:228-235. https://doi.org/10.1016/j.sajb.2020.10.017
Chattopadhyay S, Choudhury S, Roy A, Chainy GB, Samanta L (2010). T3 fails to restore mitochondrial thiol redox status altered by experimental hypothyroidism in rat testis. General and Comparative Endocrinology 169(1):39-47. https://doi.org/ 10.1016/j.ygcen.2010.07.014
Darabpour E, Motamedi H, Nejad SMS (2010). Antimicrobial properties of Teucrium polium against some clinical pathogens. Asian Pacific Journal of Tropical Medicine 3(2):124-127.
De Oliveira VM, Ivanski F, de Oliveira IM, Bargi-Souza P, Schiessel DL, Romano M A, Romano RM (2020). Acrylamide induces a thyroid allostasis–adaptive response in prepubertal exposed rats. Current Research in Toxicology 1:124-132. https://doi.org/10.1016/j.crtox.2020.10.003
Elhelaly AE, AlBasher G, Alfarraj S, Almeer R, Bahbah EI, Fouda MM, ... Abdel-Daim MM (2019). Protective effects of hesperidin and diosmin against acrylamide-induced liver, kidney, and brain oxidative damage in rats. Environmental Science and Pollution Research 26:35151-35162. https://doi.org/10.1007/s11356-019-06660-3
Elkomy A, Aboubakr M, Ibrahim S, Abdelhamid Y (2018). Protective effects of Syzygium aromaticum oil (Clove) against acrylamide induced hepatic, renal, and testicular toxicity in rats. International Journal of Pharmacology and Toxicology 6(1):12-17. https://doi.org/10.1007/s11356-019-06660-3
El-Sharouny SH, El-Enein RA, ArsaniosSF STM, Bayoumy AH (2016). Acrylamide induced liver toxicity and the possible protective role of vitamin E in adult male albino rat: histological, biochemical and histochemical study. The Egyptian Journal of Medical Sciences 37(2):727-746.
Govindaraju I, Sana M, Chakraborty I, Rahman MH, Biswas R, Mazumder N (2024). Dietary acrylamide: a detailed review on formation, detection, mitigation, and its health impacts. Foods 13(4):556. https://doi.org/10.3390/foods13040556
Gupta D, Singh S, Soni R, Gupte SS, Rathour A, Shrivastava S, Shukla S (2023). Possible metabolic effect of acrylamide on biological system. Food Safety and Health 1(2):126-138. https://doi.org/10.1002/fsh3.12020
Hamdy SM, Bakeer HM, Eskander EF, Sayed ON (2012). Effect of acrylamide on some hormones and endocrine tissues in male rats. Human and Experimental Toxicology 31(5):483-491. https://doi.org/10.1177/0960327111417267
Hasanein P, Shahidi S (2012). Preventive effect of Teucrium polium on learning and memory deficits in diabetic rats. Medical science monitor: International Medical Journal of Experimental and Clinical Research 18(1):BR41. https://doi.org/10.12659/msm.882201
Ibrahim AA, Mohammed NA, Eid KA, Abomughaid MM, Abdelazim AM, Aboregela AM (2021). Hypothyroidism: morphological and metabolic changes in the testis of adult albino rat and the amelioration by alpha-lipoic acid. Folia Morphologica 80(2):352-362. https://doi.org/10.5603/FM.a2020.0071
Ibrahim AF, Hafez LM, Yousif AB (2020). Protective role of polyphenols (anthocyanin, gallic acid) and blackberry juice against acrylamide reproductive toxicity in male rats. International Journal of Progressive Sciences and Technologies 23(2):292-300.
Jung HA, Roy A, Abdul QA, Kim HR, Park HJ, Choi JS (2017). Luteolin 5-O-glucoside from Korean milk thistle, Cirsium maackii, exhibits anti-inflammatory activity via activation of the Nrf2/HO-1 pathway. Natural Product Sciences 23(3):183-191. https://doi.org/10.20307/nps.2017.23.3.183
Kalaivani M, Saleena UV, Katapadi KGK, Kumar YP, Nayak D (2018). Effect of acrylamide ingestion on reproductive organs of adult male Wistar rats. Journal of Clinical and Diagnostic Research 12(11). https://doi.org/10.7860/JCDR/2018/38170.12364
Kalra S, Aggarwal S, Khandelwal D (2021). Thyroid dysfunction and dysmetabolic syndrome: the need for enhanced thyrovigilance strategies. International Journal of Endocrinology 2021(1):9641846. https://doi.org/10.1155/2021/9641846
Khafaji SS (2023). Antioxidant, anti-inflammatory, and anti-reprotoxic effects of kaempferol and vitamin E on lead acetate-induced testicular toxicity in male rats. Open Veterinary Journal 13(12):1683. https://doi.org/10.5455/OVJ.2023.v13.i12.17
Kucukler S, Caglayan C, Darendelioğlu E, Kandemir FM (2020). Morin attenuates acrylamide-induced testicular toxicity in rats by regulating the NF-κB, Bax/Bcl-2 and PI3K/Akt/mTOR signaling pathways. Life Sciences 261:118301. https://doi.org/10.1016/j.lfs.2020.118301
Kumar J, Das S, Teoh SL (2018). Dietary acrylamide and the risks of developing cancer: facts to ponder. Frontiers in Nutrition 5:14. https://doi.org/10.3389/fnut.2018.00014
Mahmood SA, Amin KA, Salih SF (2015). Effect of acrylamide on liver and kidneys in albino wistar rats. International Journal of Current Microbiology and Applied Sciences 4(5):434-44. https://doi.org/10.13140/RG.2.1.2508.6880
Maran RRM, Arunakaran J, Aruldhas MM (2000). T3 directly stimulates basal and modulates LH induced testosterone and oestradiol production by rat Leydig cells in vitro. Endocrine Journal 47(4):417-428. https://doi.org/10.1507/endocrj.47.417
Mohamed HM, Abd El-Twab SM (2016). Gallic acid attenuates chromium-induced thyroid dysfunction by modulating antioxidant status and inflammatory cytokines. Environmental Toxicology and Pharmacology 48:225-236. http://dx.doi.org/10.1016/j.etap.2016.08.019
Nabil I, Mady B, Solaiman A (2024). Evaluation of the probable alleviating effect of luteolin on acrylamide mediated toxicity of the caput epididymal lining epithelium in adult rats: Histological and Biochemical Study. Egyptian Journal of Histology 47(3):991-1008. https://doi.org/10.21608/ejh.2023.219557.1910
Noumi E, Snoussi M, Anouar EH, Alreshidi M, Veettil VN, Elkahoui S, ... Badraoui R (2020). HR-LCMS-based metabolite profiling, antioxidant, and anticancer properties of Teucrium polium L. methanolic extract: Computational and in vitro study. Antioxidants 9(11):1089. https://doi.org/10.3390/antiox9111089
Olasehinde O, Osawe SO, Alilonu DO, Ogunwa S, Obimma JN, Ebokaiwe AP (2025). Rutin impedes indoleamine 2, 3-dioxygenase activity/expression to mitigate heat stress-mediated testicular dysfunction. Pharmacological Research-Natural Products 6:100186. https://doi.org/10.1016/j.prenap.2025.100186
Owumi SE, Adedara IA, Akomolafe AP, Farombi EO, Oyelere AK (2020). Gallic acid enhances reproductive function by modulating oxido-inflammatory and apoptosis mediators in rats exposed to aflatoxin-B1. Experimental Biology and Medicine 245(12):1016-1028. https://doi.org/ 10.1177/1535370220936206
Özer Z, Kılıç T, Çarıkçı S, Yılmaz H (2018). Investigation of phenolic compounds and antioxidant activity of Teucrium polium L. decoction and infusion. Balıkesir Üniversitesi Fen Bilimleri Enstitüsü Dergisi 20(1):212-218. https://doi.org/10.25092/baunfbed.370594
Pourentezari M, Talebi A, Abbasi A, Khalili MA, Mangoli E, Anvari M (2014). Effects of acrylamide on sperm parameters, chromatin quality, and the level of blood testosterone in mice. Iranian Journal of Reproductive Medicine 12(5):335.
Rahmouni F, Daoud S, Rebai T (2019). Teucrium polium attenuates carbon tetrachloride‐induced toxicity in the male reproductive system of rats. Andrologia 51(2):e13182. https://doi.org/10.1111/and.13182
Rahmouni F, Hamdaoui L, Rebai T (2017). In vivo anti-inflammatory activity of aqueous extract of Teucrium polium against carrageenan-induced inflammation in experimental models. Archives of Physiology and Biochemistry 123(5):313-321. https://doi.org/10.1080/13813455.2017.1333517
Rahmouni F, Saoudi M, Amri N, El-Feki A, Rebai T, Badraoui R (2018). Protective effect of Teucrium polium on carbon tetrachloride induced genotoxicity and oxidative stress in rats. Archives of Physiology and Biochemistry 124(1):1-9. https://doi.org/10.1080/13813455.2017.1347795
Rifai L, Saleh FA (2020). A review on acrylamide in food: Occurrence, toxicity, and mitigation strategies. International Journal of Toxicology 39(2):93-102. https://doi.org/ 10.1177/1091581820902405
Romano RM, Gomes SN, Cardoso NCS, Schiessl L, Romano MA, Oliveira CA (2017). New insights for male infertility revealed by alterations in spermatic function and differential testicular expression of thyroid-related genes. Endocrine 55:607-617. https://doi.org/10.1007/s12020-016-0952-3
Seify M, Abedpour N, Talebi SF, Hazari V, Mehrara M, Koohestanidehaghi Y, ... Bhandari RK (2024). Impacts of Acrylamide on testis and spermatozoa. Molecular Biology Reports 51(1):739. https://doi.org/10.1007/s11033-024-09677-1
Sengul E, Gelen V, Yildirim S, Cinar İ, Aksu EH (2023). Effects of naringin on oxidative stress, inflammation, some reproductive parameters, and apoptosis in acrylamide‐induced testis toxicity in rat. Environmental Toxicology 38(4):798-808. https://doi.org/10.1002/tox.23728
Shahrzad E, Shariati M, Naeimi S, Edalatmanesh MA (2021). Effects of N-Acetylcysteine on FAS gene expression level in testicular tissue of acrylamide-treated adult rats. Journal of Advanced Biomedical Sciences 11(2):3848-3856. https://orcid.org/0000-0001-7360-0208
Sharififar F, Dehghn-Nudeh G, Mirtajaldini M (2009). Major flavonoids with antioxidant activity from Teucrium polium L. Food Chemistry 112(4):885-888. https://doi.org/10.1016/j.foodchem.2008.06.064
Sharma A, Jain J (2008). Effects of oral exposure of acrylamide on plasma levels of thyroid hormones and haematological parameters in the Swiss albino mice. Asian Journal of Experimental Sciences 22(3):317-324.
Suvarna SK, Layton C, Bancroft JD (2012). Theory and practice of histological techniques. Elsevier Health, Sciences.
Timizar Z, Boutemak K, Hadj Ziane-Zafour A, Touzout N, Tahraoui H, Jaouadi B, ... Amrane A (2024). Comprehensive analysis of phytochemical composition, antioxidant potential, and antibacterial activity of T. polium. Separations 11(4):90. https://doi.org/10.3390/separations11040090
Toplan GG, Göger F, Taşkin T, Genç GE, Civaş A, İşcan G, ... Başer KHC (2022). Phytochemical composition and pharmacological activities of Teucrium polium L. collected from eastern Turkey. Turkish Journal of Chemistry 46(1):269-282. https://doi.org/10.3906/kim-2107-13
WHO (World Health Organization) (1993). Laboratory manual: Analysis of human semen and sperm-cervical mucus interaction. 3 rd ed. Cambridge Univerisity Press. Cambridge, UK.
Xia N, Chen G, Liu M, Ye X, Pan Y, Ge J, ... Xie S (2016). Anti-inflammatory effects of luteolin on experimental autoimmune thyroiditis in mice. Experimental and Therapeutic Medicine 12(6):4049-4054. https://doi.org/10.3892/etm.2016.3854
Yan F, Wang L, Zhao L, Wang C, Lu Q, Liu R (2023). Acrylamide in food: Occurrence, metabolism, molecular toxicity mechanism and detoxification by phytochemicals. Food and Chemical Toxicology 175:113696. https://doi.org/10.1016/j.fct.2023.113696
Yildirim S, Sengul E, Aksu EH, Cinar İ, Gelen V, Tekin S, Dag Y (2024). Selenium reduces acrylamide‐induced testicular toxicity in rats by regulating HSD17B1, StAR, and CYP17A1 expression, oxidative stress, inflammation, apoptosis, autophagy, and DNA damage. Environmental Toxicology 39(3):1402-1414. https://doi.org/10.1002/tox.23996
Yilmaz BO, Yildizbayrak N, Aydin Y, Erkan M (2017). Evidence of acrylamide-and glycidamide-induced oxidative stress and apoptosis in Leydig and Sertoli cells. Human and Experimental Toxicology 36(12):1225-1235. https://doi.org/10.1177/0960327116686818
Zhang J, Zhu X, Xu W, Hu J, Shen Q, Zhu D, ... Cao Y (2023). Exposure to acrylamide inhibits testosterone production in mice testes and Leydig cells by activating ERK1/2 phosphorylation. Food and Chemical Toxicology 172:113576. https://doi.org/10.1016/j.fct.2022.113576
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