1.Aphrodisiac Effects of Aqueous Extracts of Pausinystalia yohimbe, Cassia sieberiana and Cissus populnea Roots In Paroxetine-Induced Sexual Dysfunction Male Rats: A Comparative Study:
Musa T. Yakubu ; Adeshola I. Adebiyi ; Quadri O. Nurudeen
Pacific Journal of Medical Sciences 2019;20(1):30-42
There is a folkloric claim that Pausinystalia yohimbe,Cassia sieberiana and Cissus populnearoots can be used to enhance sexual behaviour in male rats. However, there is still dearth of scientific evidence that substantiated the acclaimed efficacy of separate and combined use of the plant as sex enhancer. Therefore, the aims of this study were to compare the separate and combined effects of aqueous extracts of Pausinystalia yohimbe, Cassia sieberiena and Cissus populnearoots in paroxetine-induced sexually impaired male rats.Thirty five male rats were assigned into seven groups (A-G) such that rats in group A received orally 1.0 ml of distilled water for 7 days, while those in groups B -G which were induced into sexual dysfunction (administration of 10 mg/kg of paroxetine) also received equal volume of distilled water, 7.14 mg/kg body weight of PowmaxM (a reference drug), 50 mg/kg body weight of P. yohimbe, 50 mg/kg body weight of C. sieberiana, 50 mg/kg body weight of C. populneaand 50 mg/kg body weight of 1:1:1 mixture of the three extracts, once daily for seven days respectively. The sexual behavior indices of the male rats and the levels of their reproductive hormones were evaluated by standard procedures. The paroxetine-treatment related reductions (P<0.05) in the sexual behaviour indices of Mount Frequency, Intromission Frequency and Ejaculatory Frequency, levels of serum reproductive hormones of testosterone, luteinizing hormone and follicle stimulating hormone were progressively attenuated by the separate administration of the plant extracts. Furthermore, the increases in the Mount Latency, Intromission Latency, Ejaculatory Latency and Post-ejaculatory Interval were also gradually reduced, following the administration of the plant extracts. The male rat sexual behaviour indices and the levels of the male reproductive hormones following the administration of the 1:1:1 mixture of the extracts were not significantly different (P>0.05) from the effects of the separate extracts. All these changes compared favourably (P>0.05) well with those of the sexual dysfunction rats that received PowmaxM (Group G). The results obtained in the present study indicate that the extracts of these plants may have the potentialfor the management of sexual dysfunction in male rats. The combined use of the plants was not significantly better than the individual use of the plants thereby, each and any of the three plants readily available might be used for this purpose.
Aphrodisiacs
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Animals
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Phytotherapy
2.The Effects of Ginseng Saponin on Rabbit Cavernosal Smooth Muscle Relaxation in vitro.
Hyung Jee KIM ; Gil Ho LEE ; Je Jong KIM
Korean Journal of Urology 1998;39(5):443-449
PURPOSE: Ginseng saponin, the active ingredients extracted from Panax ginseng, has been used as aphrodisiacs in oriental country, however the exact action mechanism of ginseng saponin still remains uncertain. This study was undertaken to see if ginseng crude saponin(GCS) induce the L-arginine/Nitric oxide(NO) pathway related the corpus cavernosal smooth muscle relaxation, and to obtain the fundamental data for clinical application. MATERIALS AND METHODS: Isometric tension changes of rabbit corpus cavernosal strip to various drugs and electrical stimulation in an organ chamber(volume:30m1) were recorded with a pressure transducer. RESULTS: GCS(0.2-8.0mg) relaxed the smooth muscle of rabbit corpus cavernosum (SMRCC) precontracted with phenylephrine(10(-5)M) in dose-dependent manner GCS at the concentration of 0.75mg significantly enhanced the relaxation of corpus cavernosum induced by the electrical field stimulation. GCS(0.2-8.0mg)-induced relaxation was significantly attenuated by atropine(10(-6)M), methylene blue(10(-4)M) and L-NAME(10(-5)M), but there was no significant change of GCS-induced relaxation of SMRCC by adding VIP antagonist or indomethacin. In addition, the inhibition of GCS-induced relaxation of SMRCC by methylene blue or L-NAME was greater than that by atropine. CONCLUSIONS: These data suggest that GCS, as a NO donor, induces the relaxation of SMRCC through the L-arginine/NO pathway. For the clinical application of GCS, further studies should be needed to clarify the subfraction of GCS.
Aphrodisiacs
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Atropine
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Electric Stimulation
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Humans
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Indomethacin
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Methylene Blue
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Muscle, Smooth*
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NG-Nitroarginine Methyl Ester
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Panax*
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Relaxation*
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Saponins*
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Tissue Donors
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Transducers, Pressure
3.A case of methemoglobinemia after ingestion of an aphrodisiac, later proven as dapsone.
Seoung Woo LEE ; Ji Young LEE ; Kyung Joo LEE ; Myungsoo KIM ; Moon Jae KIM
Yonsei Medical Journal 1999;40(4):388-391
Methemoglobin (MetHb) is an oxidation product of hemoglobin in which the sixth coordination position of ferric iron is bound to a water molecule or to a hydroxyl group. The most common cause of acquired MetHb-emia is accidental poisoning which usually is the result of ingestion of water containing nitrates or food containing nitrite, and sometimes the inhalation or ingestion of butyl or amyl nitrite used as an aphrodisiac. We herein report a case of MetHb-emia after ingestion of an aphrodisiac, later identified as dapsone by gas chromatograph/mass selective detector (GC/MSD). A 24-year old male was admitted due to cyanosis after ingestion of a drug purchased as an aphrodisiac. On arterial blood gas analysis, pH was 7.32, PaCO2 26.8 mmHg, PaO2 75.6 mmHg, and bicarbonate 13.9 mmol/L. Initial pulse oxymetry was 89%. With 3 liter of nasal oxygen supplement, oxygen saturation was increased to 90-92%, but cyanosis did not disappear. Despite continuous supplement of oxygen, cyanosis was not improved. On the fifth hospital day, MetHb was 24.9%. Methylene blue was administered (2 mg/kg intravenously) and the patient rapidly improved. We proved the composition of aphrodisiac as dapsone by the method of GC/MSD.
Administration, Oral
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Adult
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Antidotes/therapeutic use
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Aphrodisiacs/adverse effects*
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Case Report
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Cyanosis/drug therapy
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Cyanosis/chemically induced
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Cyanosis/blood
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Dapsone/adverse effects*
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Human
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Male
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Methemoglobinemia/drug therapy
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Methemoglobinemia/chemically induced*
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Methylene Blue/therapeutic use
4.Plant-based Rasayana drugs from Ayurveda.
Subramani Paranthaman BALASUBRAMANI ; Padma VENKATASUBRAMANIAN ; Subrahmanya Kumar KUKKUPUNI ; Bhushan PATWARDHAN
Chinese journal of integrative medicine 2011;17(2):88-94
Rasayana tantra is one of the eight specialties of Ayurveda. It is a specialized practice in the form of rejuvenative recipes, dietary regimen, special health promoting behaviour and drugs. Properly administered Rasayana can bestow the human being with several benefits like longevity, memory, intelligence, freedom from diseases, youthful age, excellence of luster, complexion and voice, optimum strength of physique and sense organs, respectability and brilliance. Various types of plant based Rasayana recipes are mentioned in Ayurveda. Review of the current literature available on Rasayanas indicates that anti-oxidant and immunomodulation are the most studied activities of the Rasayana drugs. Querying in Pubmed database on Rasayanas reveals that single plants as well as poly herbal formulations have been researched on. This article reviews the basics of Rasayana therapy and the published research on different Rasayana drugs for specific health conditions. It also provides the possible directions for future research.
Animals
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Anti-Ulcer Agents
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pharmacology
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therapeutic use
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Antineoplastic Agents, Phytogenic
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pharmacology
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therapeutic use
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Antiparasitic Agents
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pharmacology
;
therapeutic use
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Aphrodisiacs
;
pharmacology
;
therapeutic use
;
Free Radical Scavengers
;
pharmacology
;
therapeutic use
;
Giardiasis
;
drug therapy
;
Herbal Medicine
;
classification
;
methods
;
trends
;
Humans
;
Immunologic Factors
;
pharmacology
;
therapeutic use
;
Medicine, Ayurvedic
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Models, Biological
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Neuroprotective Agents
;
pharmacology
;
therapeutic use
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Plant Preparations
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classification
;
therapeutic use
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Radiation-Protective Agents
;
pharmacology
;
therapeutic use