M Wankeu-Nya1, P Watcho2, T B Nguelefack3, M Carro-Juarez4, L Tapondjou5, A Kamanyi3. 1. Animal Physiology and Phytopharmacology Laboratory, Department of Animal Biology, University of Dschang, P.O. BOX 67 Dschang-Cameroon; Laboratory of Animal Biology and Physiology, Department of Animal Organisms Biology, University of Douala, P.O. BOX 24157, Douala-Cameroon. 2. Animal Physiology and Phytopharmacology Laboratory, Department of Animal Biology, University of Dschang, P.O. BOX 67 Dschang-Cameroon. Electronic address: pwatcho@yahoo.fr. 3. Animal Physiology and Phytopharmacology Laboratory, Department of Animal Biology, University of Dschang, P.O. BOX 67 Dschang-Cameroon. 4. Laboratorio de Comportamiento Reproductivo, Escuela de Medicina Veterinaria y Zootecnia, Universidad Autónoma de Tlaxcala, Tlaxcala, C.P. 90000, Mexico. 5. Organic Chemistry Laboratory, Department of chemistry, University of Dschang, P.O. BOX 67 Dschang-Cameroon.
Abstract
OBJECTIVE: To investigate the effects of Dracaena arborea (D. arborea) on the sexual behavior parameters in experienced type-1 diabetic rats. METHODS: Aqueous and ethanol (100 and 500 mg/kg respectively) extracts of dried root barks of D. arborea, sildenafil citrate (1.44 mg/kg), trimethylamine-N-oxide (TMAO, 20 mg/kg) and distilled water (10 mL/kg) were orally administered to 4 weeks streptozotocin-induced diabetic rats. Mount latency and frequency (ML, MF), intromission latency and frequency (IL, IF) and post-ejaculatory interval (PEI) were measured by ejaculatory series during 90 min once a week for 4 weeks. Glycemia was determined at the beginning and at the end of the treatment. RESULTS: D. arborea did not show any major antihyperglycemic effects. Compared to the control group, a significant (P<0.05-0.001) increase in MF and IF was noticed in rats treated with sildenafil citrate (89.71% and 90.07% respectively), aqueous (500 mg/kg, 88.08% and 88.74% respectively) and ethanol (100 mg/kg; 89.53% and 89.17 respectively) extracts of D. arborea after two weeks (series 1) of treatment. ML, IL and PEI were significantly (P<0.05-0.001) decreased after 4 weeks of daily treatment [sildenafil citrate (96.31, 96.31% and 34.98%), and D. arborea aqueous 500 mg/kg (94.33, 94.33% and 66.60%) and ethanol extracts 100 mg/kg (96.98, 97.08% and 64.26%)]. CONCLUSIONS: These aphrodisiac potentials of D. arborea in experienced diabetic rats could be due to the antioxidant and androgenic properties of phenols, flavonoids, saponins and sterols revealed in the plant extracts.
OBJECTIVE: To investigate the effects of Dracaena arborea (D. arborea) on the sexual behavior parameters in experienced type-1 diabeticrats. METHODS: Aqueous and ethanol (100 and 500 mg/kg respectively) extracts of dried root barks of D. arborea, sildenafil citrate (1.44 mg/kg), trimethylamine-N-oxide (TMAO, 20 mg/kg) and distilled water (10 mL/kg) were orally administered to 4 weeks streptozotocin-induced diabeticrats. Mount latency and frequency (ML, MF), intromission latency and frequency (IL, IF) and post-ejaculatory interval (PEI) were measured by ejaculatory series during 90 min once a week for 4 weeks. Glycemia was determined at the beginning and at the end of the treatment. RESULTS:D. arborea did not show any major antihyperglycemic effects. Compared to the control group, a significant (P<0.05-0.001) increase in MF and IF was noticed in rats treated with sildenafil citrate (89.71% and 90.07% respectively), aqueous (500 mg/kg, 88.08% and 88.74% respectively) and ethanol (100 mg/kg; 89.53% and 89.17 respectively) extracts of D. arborea after two weeks (series 1) of treatment. ML, IL and PEI were significantly (P<0.05-0.001) decreased after 4 weeks of daily treatment [sildenafil citrate (96.31, 96.31% and 34.98%), and D. arborea aqueous 500 mg/kg (94.33, 94.33% and 66.60%) and ethanol extracts 100 mg/kg (96.98, 97.08% and 64.26%)]. CONCLUSIONS: These aphrodisiac potentials of D. arborea in experienced diabeticrats could be due to the antioxidant and androgenic properties of phenols, flavonoids, saponins and sterols revealed in the plant extracts.
Authors: Modeste Wankeu-Nya; Adrian Florea; Ştefana Bâlici; Horea Matei; Pierre Watcho; Albert Kamanyi Journal: J Tradit Complement Med Date: 2019-09-17