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Eremomastax speciosa potentializes the PMSG-inducing effect on some physiological and biochemical parameters in PMSG-primed immature rats

Published online by Cambridge University Press:  12 August 2020

Gildas Tetaping Mbemya*
Affiliation:
State University of Ceará, Faculty of Veterinary Sciences, LAMOFOPA, Fortaleza, CE, Brazil University of Dschang, Faculty of Science, Department of Biochemistry, URBPMAN, Dschang, Cameroon
Marie Stéphanie Goka Chekem
Affiliation:
University of Dschang, Faculty of Science, Department of Biochemistry, URBPMAN, Dschang, Cameroon
Landry Lienou Lienou
Affiliation:
University of Dschang, Faculty of Science, Department of Biochemistry, URBPMAN, Dschang, Cameroon
Njina Nguedia Sylvain
Affiliation:
University of Dschang, Faculty of Science, Department of Biochemistry, URBPMAN, Dschang, Cameroon
Jiatsa Nathalie Donfack
Affiliation:
Free University of Brussels, Research Laboratory on Human Reproduction, Brussels, Belgium
Denise Damasceno Guerreiro
Affiliation:
State University of Ceará, Faculty of Veterinary Sciences, LAMOFOPA, Fortaleza, CE, Brazil
Jacques Romain Njimou
Affiliation:
University of Ngaoundéré, School of Chemical Engineering and Mineral Industries, Ngaoundéré, Cameroon
Ana Paula Ribeiro Rodrigues
Affiliation:
State University of Ceará, Faculty of Veterinary Sciences, LAMOFOPA, Fortaleza, CE, Brazil
Phélix Bruno Telefo
Affiliation:
University of Dschang, Faculty of Science, Department of Biochemistry, URBPMAN, Dschang, Cameroon
*
Author for correspondence: Gildas Tetaping Mbemya. Programa de Pós-Graduação em Biotecnologia (PPGB-RENORBIO-UECE). Laboratório de Manipulação de Oócitos e Folículos Pré-Antrais (LAMOFOPA), Universidade Estadual do Ceará (UECE), Av. Dr. Silas Munguba, 1700, Campus do Itaperi, Fortaleza – CE – Brasil. CEP: 60 714 903. Tel: +55 85 3101 9852. Fax: +55 85 3101 9840/ URBPMAN, Department of Biochemistry, Faculty of Science, P.O. Box 67, UDs, Dschang, Cameroon. E-mail: gildasmbemya@yahoo.fr

Summary

The present study evaluated the effect of the aqueous extract from leaves of E. speciosa on some physiological and biochemical parameters of reproduction and the onset of puberty in pregnant mare serum gonadotropin (PMSG)-primed immature female rats. High pressure liquid chromatography (HPLC) was used to quantify the phenolic compounds in the methanol/methylene chloride (1:1) extract, the ethanolic and ethyl acetate fractions and the aqueous residue of E. speciosa. E. speciosa (0, 8, 32 or 64 mg/kg) were administered for 15 days to 24 non-PMSG-primed and 24 primed rats with 0.01 IU of PMSG. At the end of the treatment period, animal were sacrificed and their body, ovarian, uterine weight, ovarian protein or cholesterol level, as well as data on puberty onset were recorded. Of the 16 polyphenolic compounds quantitatively revealed in the extracts and fractions of E. speciosa after HPLC analysis, quercetin, rutin, apigenin and eugenol were the most abundant. Non-primed rats showed a significant increase (P < 0.05) in the uterine relative weight at the dose of 8 mg/kg when compared with the other treatments. The uterine proteins and the ovarian cholesterol (P < 0.05), respectively, showed a reduction at doses of 64 mg/kg and 32 mg/kg in non-primed rats. However in PMSG-primed rats, a significant decrease (P < 0.05) was observed in ovarian cholesterol at 64 mg/kg. In conclusion, E. speciosa potentializes the PMSG-inducing effect on folliculogenesis in PMSG-primed rats.

Type
Research Article
Copyright
© The Author(s), 2020. Published by Cambridge University Press

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References

Ali, F, Naz, F, Jyoti, S and Siddique, YH (2014). Protective effect of apigenin against nitrosodiethylamine (NDEA)-induced hepatotoxicity in albino rats. Mutat Res 767, 1320.CrossRefGoogle ScholarPubMed
Ali, F, Rahul, , Naz, F, Jyoti, S and Siddique, YH (2017). Health functionality of apigenin: a review. Int J Food Prop 20, 1197–238.CrossRefGoogle Scholar
Allan, CM, Kalak, R, Dunstan, CR, McTavish, KJ, Zhou, H, Handelsman, DJ and Seibel, MJ (2010). Follicle-stimulating hormone increases bone mass in female mice. Proc Natl Acad Sci USA 52, 22629–34.CrossRefGoogle Scholar
Baldwin, D and Mayers, A (2003). Sexual side effects of antidepressant and antipsychotic drugs. Adv Psychiatr Treat 9, 202–10.CrossRefGoogle Scholar
Barberino, RS, Barros, VR, Menezes, VG, Santos, LP, Araújo, VR, Queiroz, MA, Almeida, JR, Palheta, RC and Matos, MH (2016). Amburana cearensis leaf extract maintains survival and promotes in vitro development of ovine secondary follicles. Zygote 24, 277–85.CrossRefGoogle ScholarPubMed
Bradford, MM (1976). A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72, 248–54.CrossRefGoogle Scholar
Braw, RH and Tsafriri, A (1980). Effect of PMSG on follicular atresia in the immature rat ovary. J Reprod Fertil 59, 267–72.CrossRefGoogle ScholarPubMed
Counis, R, Combarnous, Y, Chabot, V and Taragnat, C (2001). Regulation of the synthesis and release of pituitary gonadotropins. In Reproduction in mammals and humans, vol. 3. (eds Thibault, C and Levasseur, MC). INRA, Ellipses Paris, pp. 6584.Google Scholar
De Oliveira, DH, Fighera, TM, Bianchet, LC, Kulak, CA and Kulak, J (2012). Androgens and bone. Minerva Endocrinol 4, 305–14.Google Scholar
Dierich, A, Sairam, MR, Monaco, L, Fimia, GM, Gansmuller, A, LeMeur, M, Sassone-Corsi, P (1998). Impairing follicle-stimulating hormone (FSH) signaling in vivo: targeted disruption of the FSH receptor leads to aberrant gametogenesis and hormonal imbalance. Proc Natl Acad Sci USA 95, 13612–7.CrossRefGoogle ScholarPubMed
Goka, MSC, Telefo, PB, Mbemya, GT, Awouafack, MD, Lienou, LL, Yemele, DM, Njina, SN Donfack, NJ, Tagne, RS and Fekam, FB (2016). Potentialization of pregnant mare serum gonadotropin inducing effect on ovarian follicles growth by the aqueous extract of Aloe buettneri, Dicliptera verticillata, Hibiscus macranthus and Justicia insularis leaves in immature rats. Pharmacolology 7, 328–36.Google Scholar
Gouveia, BB, Macedo, TJ, Santos, JM, Barberino, RS, Menezes, VG, Müller, MC, Almeida, JR, Figueiredo, JR and Matos, MH (2016). Supplemented base medium containing Amburana cearensis associated with FSH improves in vitro development of isolated goat preantral follicles. Theriogenology 86, 1275–84.CrossRefGoogle ScholarPubMed
Hidalgo, M, Martin-Santamaria, S, Recio, I, Sanchez-Moreno, C, de Pascual-Teresa, B, Rimbach, G and Pascual-Teresa, S (2012). Potential anti-inflammatory, anti-adhesive, anti/estrogenic, and angiotensin-converting enzyme inhibitory activitiesof anthocyanins and their gut metabolites. Genes Nutr 7, 295306.CrossRefGoogle Scholar
Hosseinzadeh, H and Nassiri-Asl, M (2014). Review of the protective effects of rutin on the metabolic function as an important dietary flavonoid. J Endocrinol Invest 37, 783–8.CrossRefGoogle ScholarPubMed
Hsu, CY, Shih, HY, Chia, YC, Lee, CH, Ashida, H, Lai, YK and Weng, CF (2014). Rutin potentiates insulin receptor kinase to enhance insulin-dependent glucose transporter 4 translocation. Mol Nutr Food Res 58, 1168–76.CrossRefGoogle ScholarPubMed
Jahan, S, Munir, F, Razak, S, Mehboob, A, Ain, QI, Ullah, H, Afsar, T, Shaheen, G and Almajwal, A (2016). Ameliorative effects of rutin against metabolic, biochemical and hormonal disturbances in polycystic ovary syndrome in rats. J Ovarian Res 9, 86.CrossRefGoogle ScholarPubMed
Leiva-Revilla, J, LIMA, LF, Castro, SV, Campello, CC, Araújo, VR, Celestino, JJ, Pessoa, OD Silveira, E, Rodrigues, AP and Figueiredo, JR (2016). Fraction of Auxemma oncocalyx and oncocalyxone A affects the in vitro survival and development of caprine preantral follicles enclosed in ovarian cortical tissue. Forsch Komplementmed 23, 307–13.CrossRefGoogle ScholarPubMed
Leiva-Revilla, J, Cadenas, J, Vieira, AL, Macedo, V, Campello, CC, Aguiar, FL, Celestino, JJH, Pessoa, ODL, Apgar, GA, Rodrigues, APR, Figueiredo, JR and Maside, C (2017). Toxicity effect of Auxemma oncocalyx fraction and its active principle oncocalyxone A on in vitro culture of caprine secondary follicles and in vitro oocyte maturation. Semin Cienc Agrar 38, 1361–74.CrossRefGoogle Scholar
Lienou, LL, Telefo, PB. Bayala, B, Yemele, MD, Lemfack, MC, Mouokeu, C, Goka, CS, Tagne, SR and Moundipa, FP (2010). Effect of ethanolic extract of Senecio biafrae on puberty onset and fertility in immature female rat. Cameroon J Exp Biol 2, 101–9.Google Scholar
Lienou, LL, Telefo, PB, Bale, B, Yemele, D, Tagne, RS, Goka, SC, Lemfack, CM, Mouokeu, C and Moundipa, PF (2012). Effect of the aqueous extract of Senecio biafrae (Oliv. and Hiern) J. Moore on sexual maturation of immature female rat. Complement Altern Med 6, 1236.Google Scholar
Liu, RH (2004). Potential synergy of phytochemicals in cancer prevention: mechanism of action. J Nutr 134, 3479–85.CrossRefGoogle ScholarPubMed
Mbemya, GT, Guerreiro, DD, Donfack, NJ, Silva, LM, Vieira, LA, Sousa, GFC, Alves, B.G., Izaguirry, AP, Santos, FW, Telefo, PB, Pessoa, ODL, Johan, S, Figueiredo, JR and Rodrigues, APR (2017). Justicia insularis improves the in vitro survival and development of ovine preantral follicles enclosed in ovarian tissue. J Pharm Pharmacol 5, 668–80.Google Scholar
Mbemya, GT, Cadenas, J, Ribeiro de Sá, NA, Damasceno Guerreiro, D, Donfack, NJ, Alberto Vieira, L, Canafístula de Sousa, FG, Geraldo Alves, B, Lobo, CH, Santos, FW, Lima Pinto, FDC, Loiola Pessoa, OD, Smitz, J, Comizzoli, P, Figueiredo, JR and Rodrigues, APR (2018). Supplementation of in vitro culture medium with FSH to grow follicles and mature oocytes can be replaced by extracts of Justicia insularis . PLoS One 12, 121.Google Scholar
Middleton, E, Kandaswami, C and Theoharides, TC (2000). The effects of plant flavonoids on mammalian cells: implications for inflammation, heart disease, and cancer. Pharmacol Rev 52, 673751.Google ScholarPubMed
Miean, KH and Mohamed, S (2001). Flavonoid (myricetin, quercetin, kaempferol, luteolin, and apigenin) content of edible tropical plants. J Agric Food Chem 49, 3106–12.CrossRefGoogle ScholarPubMed
Moon, JY, Choi, MH and Kim, J (2016). Metabolic profiling of cholesterol and sex steroid hormones to monitor urological diseases. Endocr Relat Cancer 10, 455–67.CrossRefGoogle Scholar
Moore, WT and Ward, DN (1980). Pregnant mare serum gonadotropin. Rapid chromatographic procedures for the purification of intact hormone and isolation of subunits. J Biol Chem 255, 6923–9.Google ScholarPubMed
Navarro, VM, Fernandez-Fernandez, R, Castellano, JM, Roa, J, Mayen, AL, Gaytan, F, Aguilar, E, Pinilla, L, Dieguez, C and Tena-Sempere, M (2004). Advanced vaginal opening by precocious activation of the reproductive axis by KISS-1 peptide, the endogenous ligand of GPR54. J Physiol Soc 561, 379–86.CrossRefGoogle ScholarPubMed
Nicholas, C, Batra, S, Vargo, MA, Voss, OH, Gavrilin, MA, Wewers, MD, Guttridge, DC, Grotewold, E, Doseff, AI (2007). Apigenin blocks lipopoly-saccharide induced lethality in vivo and proinflammatory cytokines expression by inactivating NF-κB through the suppression of p65 phosphorylation. J Immunol 179, 7121–7.CrossRefGoogle Scholar
Oben, JE, Assi, SE, Agbor, GA, Musoro, DF (2006). Effect of Eremomastax speciosa on experimental diarrhea. Afr J Tradit Complenet Altern Med 3, 95100.Google Scholar
Radzikowski, C (2006). Protection of animal research subjects. Sci Eng Ethics 1, 103–10.CrossRefGoogle Scholar
Rates, SMK (2001). Plants as source of drugs. Toxicon 39, 603–13.CrossRefGoogle ScholarPubMed
Rezaei-Seresht, H, Cheshomi, H, Falanji, F, Movahedi-Motlagh, F, Hashemian, M and Mireskandari, E (2019). Cytotoxic activity of caffeic acid and gallic acid against MCF-7 human breast cancer cells: an in silico and in vitro study. Avicenna J Phytomed 9, 574–86.Google Scholar
Richmond, W (1973). Preparation and properties of cholesterol oxidase from Ocurdia Sp, and its application to enzymatic assay of total cholesterol in serum. Clin Chem 19, 1350–6.CrossRefGoogle ScholarPubMed
Simoni, M, Huhtaniemi, I, Santi, D and Casarini, L (2019). Editorial: Follicle-stimulating hormone: fertility and beyond. Front Endocrinol (Lausanne) 6, 13.Google Scholar
Singh, P, Mishra, SK, Noel, S, Sharma, S and Rath, SK (2012). Acute exposure of apigenin induces hepatotoxicity in Swiss mice. PLoS One 7, 111.Google ScholarPubMed
Skibola, CF (2004). The effect of Fucus vesiculosus, an edible brown seaweed, upon menstrual cycle length and hormonal status in three premenopausal women: a case report. J Altern Complement Med 10, 18.Google Scholar
Sun, L, Peng, Y, Sharrow, AC, Iqbal, J, Zhang, Z, Papachristou, DJ, Zaidi, S, Zhu, LL, Yaroslavskiy, BB, Zhou, H, Zallone, A, Sairam, MR, Kumar, TR, Bo, W, Braun, J, Cardoso-Landa, L, Schaffler, MB, Moonga, BS, Blair, HC and Zaidi, M (2006). FSH directly regulates bone mass. Cell 125, 247–60.CrossRefGoogle ScholarPubMed
Tagne, RS, Telefo, PB, Njina, SN, Bala, B, Goka, SMC, Yemele, DM, Lienou, LL, Mbemya, GT, Donfack, NJ, Kamdje, AHN and Moundipa, AF (2014). In vivo anti-androgenic, anti-estrogenic and antioxidant activities of the aqueous extract of Eremomastax speciosa . Asian Pac J Trop Dis 4, 952–6.CrossRefGoogle Scholar
Telefo, PB, Moundipa, PF, Tchana, AF, Tchouanguep, DC and Mbiapo, FT (1998). Effects of aqueous extract of Aloe buettneri, Dicliptera verticillata, Hibiscus macranthus, and Justicia insularis on some biochemical and physiological parameters of reproduction in immature female rat. J Ethnopharmacol 63, 193200.CrossRefGoogle Scholar
Telefo, PB, Tagne, SR, Koona, OES, Yemele, DM and Tchouanguep, FM (2012). Effect of the aqueous extract of Justicia insularis T. Anders (Acanthaceae) on ovarian folliculogenesis and fertility of female rats. Afr J Tradit Complement Altern Med 9, 197203.CrossRefGoogle Scholar
Telefo, PB, Lienou, LL, Bayala, B, Yemele, MD, Lemfack, MC, Mouokeu, C, Goka, CS, Tagne, SR and Moundipa, FP (2011). Ethnopharmacological survey of plants used for the treatment of female in fertility in Baham, Cameroon. J Ethnopharmacol 136, 178–87.CrossRefGoogle Scholar
Tohei, A, Sakamoto, S and Kogo, H (2000). Dexamethasone or triamcinolone increases follicular development in immature female rats. Japan J Pharmacol 84, 281–6.CrossRefGoogle ScholarPubMed
Tsobou, R, Mapongmetsem, PM and Van Damme, P (2016). Medicinal plants used for treating reproductive health care problems in Cameroon, Central Africa. Econ Bot 70, 145–59.CrossRefGoogle Scholar
Worthington, CA and Kennedy, J (1979). Ovarian response to exogenous hormones in six-week-old lambs. Aust J Biol Sci. 32, 91–6.CrossRefGoogle ScholarPubMed
Xiao, S, Robertson, DM and Findlay, JK (1992). Effects of activin and follicle-stimulating hormone (FSH)-suppressing protein/follistatin on FSH receptors and differentiation of cultured rat granulosa cells. Endocrinology 131, 1009–16.CrossRefGoogle ScholarPubMed
Zhang, YM and Roy, SK (2004). Downregulation of follicle-stimulating hormone (FSH)-receptor messenger RNA levels in the hamster ovary: effect of the endogenous and exogenous FSH. Biol Reprod 6, 1580–8.CrossRefGoogle Scholar