Aphrodisiac Properties Research Articles

Metabolome classification of Tongkat Ali (Eurycoma longifolia jack) and its commercial products via UHPLC-QTOF-MS-MS and its protective effect against 5-flurouracil-Induced testicular toxicity in male rats

Ethnopharmacological relevanceTongkat Ali (Eurycoma longifolia Jack) is a chief herbal medicine that is well recognized for its aphrodisiac properties, available in various commercial products worldwide. Aim of the studyThe aim of this work is to identify the different classes of secondary metabolites present in Tongkat Ali commercial products versus authenticated root, and to assess its root extract mitigative effect against 5-flurouracil (5FU)-induced testicular toxicity. Materials and methodsHigh-resolution UHPLC-QTOF-MS/MS metabolites analysis was utilized on the ethanolic Tongkat Ali extract (TAE) parallel to three Mlayasian commercial products, followed by a multivariate data analysis to understand the variability among UHPLC-MS metabolites datasets. Adult male rats were treated with 5-Fluorouracil (5FU) ± Tongkat Ali extract. Semen parameters, serum testosterone, LH, and FSH, and testicular oxidative stress biomarkers like malondialdehyde (MDA) levels, Nuclear factor kappa B (NF-κB) and erythroid 2–related factor 2 (Nrf2) were analyzed. ResultsThe main categories of secondary metabolites identified through UHPLC-MS/MS profiling were quassinoids, alkaloids, fatty acids, lignans and coumarins. Long Jack Plus® ELP-2 clustered alongside authentic roots ELR on the negative side, while Naturelle® ELP-1 and Nu-Prep-LEAKI® ELP-3 were positioned on the opposite side. The OPLS-DA model was used to identify markers for preparations from authentic roots, with commercial products enriching in ailanthone epoxide. In vivo results showed that 5FU reduced sperm parameters by 42%, while TAE improved sperm quality by 35–43% and 58–74% at dose of 400 and 800 mg/kg, respectively. Testosterone, reduced by 74% with 5FU, increased 2.3- to 3.2-fold with TAE. TAE also reduced MDA by 31–62%, NF-κB by 32–55% and increased Nrf2 by 1–2 folds. ConclusionThe manuscript presents a comparative metabolomics study and in vivo investigation into the potential of Tongkat Ali root to improve testicular function in male rats intoxicated with 5FU, an area not previously explored. Further research is required to understand the mechanisms.

A systematic review of the traditional uses, chemistry, and curative aptitude of echinacoside-a phenylethanoid glycoside.

Echinacoside (ECH), a naturally occurring water-soluble phenylethanoid glycoside, is one of the primary bioactive compounds present in several plant species, such as Echinacea, Cistanche, Plantago, Rosa, Buddleja, and Rehmannia. Research has revealed that these plants, rich in ECH, have diverse traditional uses and pharmacological activities, like anti-diabetic, anti-inflammatory, anti-fatigue, anti-allergic, anti-ageing, anti-skin glycation, analgesic, wound healing, and aphrodisiac properties. Among other activities, ophthalmic, haematopoiesis, pulmonary, anti-bacterial, anti-protozoal, anti-fungal, and anti-viral effects of ECH have been reported. Chemically, the compound comprises caffeic acid glycoside containing a trisaccharide that includes two glucose and one rhamnose unit. These units are linked through glycosidic bonds to a caffeic acid and a dihydroxyphenylethanol (hydroxytyrosol) residue, which are connected to the central rhamnose. The biosynthesis of ECH has been reported to start with forming L-phenylalanine and tyrosine precursors via the shikimic acid pathway. The structure-activity relationship of ECH has shown that various functional groups in the structure, particularly phenolic hydroxyl groups, are crucial for antioxidant activities. Similarly, in silico studies have revealed that ECH binds to different receptors, like Kelch-like ECH-associated protein 1 (Keap1), receptor for advanced glycation end products (RAGE), etc., to affect various pharmacological activities. The ECH contents in the reported plants often own these multifaceted properties, highlighting their importance in clinical research. Evident from its therapeutic efficacy, there is a huge potential for a comprehensive understanding of the mechanisms of actions of ECH, which underscores the need for more research in this area. Thus, this review is a compendium of the latest literature to analyse the existing knowledge on ECH, encompassing its distribution, traditional uses, extraction, chemical constituents, biosynthesis, pharmacological activities, structure-activity relationship, and in silico studies, following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.

Carb‐Loaded Passion: A Comprehensive Exploration of Carbohydrates in Shaping Aphrodisiac Effects

AbstractThe present overview discusses the putative aphrodisiac properties of carbohydrates. It comprehensively investigates the intricate interplay between the physiological systems that govern sexual arousal and the consumption of carbohydrates in the diet. One method to achieve this is by examining the historical origins of aphrodisiacs in various civilizations. It highlights the significance of carbohydrates as essential macronutrients and explores their function in crucial biochemical processes associated with libido and sexual response. In order to understand the impact of dietary carbs on sexual health, the study examines the correlation among sex hormones, insulin sensitivity, and blood glucose levels. To understand how particular diets high in carbohydrates can improve sexual arousal, performance and desire the analysis looks at scientific research informing that some diets have aphrodisiac properties. The present research examines the influence of carbohydrates on mood, stress levels, and overall well‐being to gain a deeper understanding of the psychological underpinnings of sexual function. The points elucidated in this analysis enhance the understanding of the complex interrelationships between dietary components, specifically carbs, and sexual health. Results have implications for lifestyle modifications aimed at improving sexual well‐being. The information contained here will also be beneficial to individuals and healthcare professionals who are looking for evidence‐based approaches to improve their sexual well‐being.

An in-depth exploration of ethnomedicinal applications, phytochemical profiles, and pharmacological potentials: unveiling Withania somnifera

Researchers have extensively studied Withania somnifera (L.) Dunal, a woody shrub renowned for its multifaceted medicinal attributes such as antibacterial, anti-inflammatory, adaptogenic, aphrodisiac, and tonifying properties, because of its medicinal and traditional values. However, comprehensive information about its medicinal uses and pharmacological implications is scattered across various sources. Thus, this study aims to provide a comprehensive review of its ethnomedicinal uses, phytochemistry, and pharmacological attributes, consolidating information from diverse data sources. Systematic investigations have revealed the presence of diverse phytochemicals in W. somnifera, including major alkaloids, withanolides, flavonoids, tannins, oils, phytosterols, and amino acids. Extracts, fractions, and bioactive compounds derived from W. somnifera exhibited potent antibacterial, anti-inflammatory, anti-aging, anti-analgesic, anti-cancer, antivenom, anti-fungal, and anti-viral activities. W. somnifera serves as a valuable source of phytochemicals with diverse biological activities, offering significant therapeutic benefits globally. However, further studies are needed to assess potential side effects. Additionally, while several isolated compounds have demonstrated notable bioactivities, future research should focus on elucidating their mechanistic features to facilitate their integration into drug discovery endeavors.

Exploration of Indonesian Herbal Plants as Aphrodisiac agents and Testing their Activity in Animal Testing

Indonesia's abundant natural resources have spurred interest in exploring certain plants believed to possess aphrodisiac properties that can enhance male libido and reproductive health. This research endeavor is designed to delve into the extraction of compounds from various plant species, followed by a comprehensive analysis of their chemical constituents. Subsequently, aphrodisiac activity assessments are conducted on male rats, focusing on key parameters such as mating frequency, climbing behavior, and coital activities. Additionally, this investigation encompasses the determination of the percentage of relative testicular weight in relation to body weight and histopathological examination of testicular organs. The findings emanating from the extracts of Piper retrofractum (PRE), Solanum melongena fruit (EE), Ocimum basilicum leaves (OBLE), Watermelon albedo (WAE), and Zingiber officinale Var Rubrum rhizoma (ZRE) reveal the presence of alkaloids, flavonoids, and saponins. Notably, EE, administered at a dosage of 30mg, yields the most prominent aphrodisiac effects in the test subjects, as evidenced by heightened mating frequency, climbing activity, and coital behaviors. Furthermore, the relative testicular weight following treatment with 30mg of PRE closely resembles the impact observed with sildenafil at a dosage of 10 mg/kgbw.

Stimulatory effect of eurycomanone from Eurycoma longifolia Jack roots on dopamine secretion in human neuroblastoma SH-SY5Y cell line

Eurycomanone has been identified as the major bioactive compound contributing to Eurycoma longifolia (EL) aphrodisiac activity, however, its mechanism of action remains obscured. Presently, eurycomanone was isolated from EL root extract and its molecular structure was identified. The human neuroblastoma SH-SY5Y cell line was differentiated into human dopaminergic neuron-like cells. Exogenous dopamine levels from the differentiated SH-SY5Y cells were quantified following the treatment of 5, 10, 15 μM of eurycomanone and 10 μM clorgyline as positive control. Dopamine secretion was significantly increased in a dose-dependent manner, compared to the vehicle control (p < .01) in differentiated SH-SY5Y cells. Dopamine concentration stimulated by 15 μM eurycomanone was significantly higher than clorgyline (p < .05), an inhibitor of monoamine oxidase A that suppresses dopamine catabolism. In conclusion, eurycomanone stimulated dopamine release of human SH-SY5Y neuron-like cells, which could be one of the mechanisms that underpin the aphrodisiac properties of the plant.

Five Underutilized Ecuadorian Fruits and Their Bioactive Potential as Functional Foods and in Metabolic Syndrome: A Review.

The Ecuadorian Amazon harbors numerous wild and cultivated species used as food, many of which are underutilized. This review explores the bioactive potential of five such fruits-Borojó (Alibertia patinoi); Chonta (Bactris gasipaes); Arazá (Eugenia stipitata); Amazon grape (Pourouma cecropiifolia), a wild edible plant; and Cocona (Solanum sessiliflorum)-and their applications against metabolic syndrome. This study highlights their health-promoting ingredients and validates traditional medicinal properties, emphasizing their significance in improving health and mitigating the effects of the Western diet. These fruits, integral to Ecuadorian cuisine, are consumed fresh and processed. Chonta is widely cultivated but less prominent than in pre-Hispanic times, Borojó is known for its aphrodisiac properties, Cocona is traditional in northern provinces, Arazá is economically significant in food products, and Amazon grape is the least utilized and researched. The fruits are rich in phenolics (A. patinoi, E. stipitata) and carotenoids (B. gasipaes, E. stipitata), which are beneficial in controlling metabolic syndrome. This study advocates for more research and product development, especially for lesser-known species with high phenolic and anthocyanin content. This research underscores the economic, cultural, and nutritional value of these fruits, promoting their integration into modern diets and contributing to sustainable agriculture, cultural preservation, and public health through functional foods and nutraceuticals.

Testing the aphrodisiac effects of Sterculia quadrifida (faloak) bark powder on male white rats (Rattus norvegicus)

Background: Sterculia quadrifida R.Br has been widely known and, empirically, has been widely used as an herbal ingredient to overcome sexual disorders in men. Objective: This study aims to assess the quality, stability, and aphrodisiac properties of faloak bark solution preparations (from plants R.Br Sterculia quadrifida) found on Timor Island, specifically on male white rats of the Wistar strain. Method: This research is a type of experimental research. The activity test used two variations of the formula (50%, 100%) extract, positive and negative control tests. Data were analysed with one-way ANOVA (p &lt; 0.05). Result: The test results of extract quality and stability, including moisture content, resting angle, flow speed, dissolving time, organoleptic test, pH, specific gravity, clarity, and homogeneity, met the requirements. The analysis results found significant differences in each test group (p &lt; 0.05), and there were substantial differences between the negative control group and the positive control group, formula one and formula two. Conclusion: The preparation of the solution of Sterculia quadrifida R. met the established quality and stability. The results of the aphrodisiac test of the effect of Sterculia quadrifida R.Br on the parameters of introduction and climbing activity showed significant activity compared to the negative control group.

Enhancement of production of glycoalkaloids by elicitors along with characterization of gene expression of pathways in Solanum xanthocarpum

Solanum xanthocarpum fruits are used in the treatment of cough, fever, and heart disorders. It possesses antipyretic, hypotensive, antiasthmatic, aphrodisiac and antianaphylactic properties. In the present study, 24 elicitors (both biotic and abiotic) were used to enhance the production of glycoalkaloids in cell cultures of S. xanthocarpum. Four concentrations of elicitors were added into the MS culture medium. The maximum accumulation (5.56-fold higher than control) of demissidine was induced by sodium nitroprusside at 50 mM concentration whereas the highest growth of cell biomass (4.51-fold higher than control) stimulated by systemin at 30 mM concentration. A total of 17 genes of biosynthetic pathways of glycoalkaloids were characterized from the cells of S. xanthocarpum. The greater accumulation of demissidine was confirmed with the expression analysis of 11 key biosynthetic pathway enzymes e.g., acetoacetic-CoA thiolase, 3- hydroxy 3-methyl glutaryl synthase, β-hydroxy β-methylglutaryl CoA reductase, mevalonate kinase, farnesyl diphosphate synthase, squalene synthase, squalene epoxidase, squalene-2,3- epoxide cyclase, cycloartenol synthase, UDP-glucose: solanidine glucosyltransferase and UDP-rhamnose: solanidine rhamno-galactosyl transferase. The maximum expression levels of UDP-rhamnose: solanidine rhamno-galactosyl transferase gene was recorded in this study.

Aphrodisiac properties of Craterispemum schweinfurthi Leaf Extract in Lead Induced Testicular Toxicity in Male Wistar Rats

Aphrodisiac properties of Craterispemum schweinfurthi Leaf Extract in Lead Induced Testicular Toxicity in Male Wistar Rats

Unveiling the Therapeutic Potential of Clitoria Guianensis (Aubl.) Benth Var. Guianensis: A Comprehensive Review of its AntiInflammatory and Wound Healing Properties

Introduction: This article proposes a comprehensive systematic review to analyze the potential of Clitoria guianensis as an anti-inflammatory and wound healing agent. The emphasis on diversifying research methods aims to deepen understanding of its medicinal properties, especially in the context of anti-inflammatory and wound healing activities. The plant, belonging to the genus Clitoria and native to Brazil, is recognized for its aphrodisiac properties and is used as a sexual stimulant, tonic, and energizer. Studies highlight the presence of bioactive compounds, such as isoflavones, which contribute to its medicinal properties. Methodology:The study was based on the Systematic Literature Review Protocol (SLRP), establishing a framework for comprehensively reviewing scientific literature. The objective was to identify the medicinal properties of C. guianensis in Brazil, focusing on its potential anti-inflammatory and wound healing properties. Results: The results of this scientific review aim to substantiate the consideration of C. guianensis as a potentially beneficial plant in tissue regeneration processes.

Pharmacological and Therapeutic Properties of Fenugreek (Trigonella foenum-graecum) Seed: A Review

Fenugreek, scientifically known as Trigonella foenum-graecum, is a versatile annual leguminous plant belonging to the Fabaceae family. It is cultivated worldwide and serves numerous purposes as a spice, herb, food, and medicine. Fenugreek is resilient and can thrive in various environments, including those with drought conditions. The plant is abundant in active constituents such as saponins, flavonoids, alkaloids, and steroids. Additionally, it is an excellent source of dietary fiber, protein, linoleic acid, linolenic acid, and vitamins A, B1, B2, and C. Fenugreek has a rich history in traditional medicine, particularly in Ayurveda, Unani, and Tibetan medicine. Studies have shown that it possesses antimicrobial, antioxidant, antidiabetic, antihyperlipidemic, antiobesity, anticancer, anti-inflammatory, carminative, aphrodisiac, and emollient properties. Moreover, its seed polysaccharide content has made it useful in the food industry as a stabilizer, adhesive, and emulsifying agent. This article provides an overview of the history, cultivation, nutritional components, nutraceutical role, safety, and toxicological properties of fenugreek. Its main aim is to summarize the benefits of this "golden seed" and its associated aspects.

Extraction, Isolation and Neuropharmacological Potential of Peristrophe bicalyculata (R.) Nees

Because of their widespread availability, low cost, low risk, and lack of side effects, medicinal herbs play a crucial role in traditional medicine all throughout the world. For medicinal purposes, Peristrophe bicalyculata (R.) is being used today. Nees as a nerve system tonic. Plant roots have antibacterial, anti-inflammatory, immunostimulating, and aphrodisiac properties. This plant root may provide health advantages, making it suitable for nutraceutical and functional food compositions. This research examined P. bicalyculata (R.) neuropharmacological effects on memory enhancement to treat cognition-related illnesses and learning and memory disorders. In phytochemical investigation, P. bicalyculata (R.) Nees ethanolic extract has higher phytoconstituents. Spectrophotometric and thin layer chromatography (TLC) plate bioassay detection showed that P. bicalyculata (R.) Nees ethanolic extract inhibits acetylcholinesterase activity. TLC and high-performance thin layer chromatography (HPTLC) were performed on P. bicalyculata (R.) Nees ethanolic extract. TLC and HPTLC spots are well resolved, indicating active ingredients in the extract. Total phenolic, flavonoid, and ascorbic content of P. bicalyculata (R.) Nees ethanolic extract was measured. Ex-vivo tests like lipid peroxidation testing reveal the extract is antioxidant. In conclusion, the ethanolic extract of P. bicalyculata (R.) Nees has memory-enhancing, antidepressant, and neuroprotective properties due to its anticholinesterase potential, effect on neurotransmitters like dopamine and serotonin, and antioxidant profile. More research is needed on its safety, effectiveness, and mechanism of action for therapeutic use.

Therapeutic potential of Nankhawah/Ajwain (Tracyspermum ammi Linn): A comprehensive review article

Background: Trachyspermum ammi Linn., commonly known as ajwain, is a widely recognized spice and medicinal plant originating from Egypt but cultivated across regions such as Iraq, Iran, Afghanistan, Pakistan, and India. Belonging to the Apiaceae family, this species offers diverse pharmacological benefits due to its rich chemical constituents.&#x0D; Objectives: This review aims to summarize the traditional and contemporary applications of Trachyspermum ammi, focusing on its ethnobotanical description, chemical composition, and pharmacological aspects.&#x0D; Methodology: The literature search encompassed scientific databases and publications covering the historical usage, chemical profiling, and biological activities of Trachyspermum ammi.&#x0D; Results: Trachyspermum ammi exhibits a variety of pharmacological activities, including antifungal, antioxidant, antimicrobial, antinociceptive, antispasmodic, carminative, diuretic, aphrodisiac, and anthelmintic properties. Traditionally, it has been employed to treat conditions such as flatulence, atonic dyspepsia, diarrhea, abdominal tumors, abdominal pain, piles, bronchial issues, lack of appetite, galactogogue, asthma, and amenorrhea as it possesses properties of Muhallil, Mudirr-i-Bawl-o-Hayd, Dafa e Tafun, Jali, Habis etc. Modern research supports these claims while also revealing its potential in treating kidney stones, abortion, and aflatoxin detoxification.&#x0D; Conclusion: Trachyspermum ammi holds great promise as a natural resource for novel therapies, owing to its extensive array of bioactive components and established pharmacological effects. Further investigation into its mechanisms of action and optimization of extraction techniques could lead to more efficient utilization of this valuable medicinal plant.&#x0D; Keywords: Ajwain, Nankhawah, Trachyspermum Ammi Linn, Mudirr-i-Bawl-o-Hayd, Hazim, Thymol, Appetizer.

Therapeutic Uses of Mee Tree (Madhuca longifolia)

In the past, our ancestors maintained a close relationship with the environment. They knew the value of many plants. One tree that our ancestors preserved is the Mee tree. Madhuca longifolia belonging to the family Sapotaceae, is one of those multipurpose forest tree species that provide an answer for the food, fodder and fuel. It is widely distributed in the South Asian countries, Especially in Sri Lanka. Mee tree is a large deciduous tree growing widely under dry tropical and sub-tropical climatic conditions. The tree has religious and aesthetic value in the tribal culture. The trees with best girth in forest are often Mee trees as it is protected and cared by forest dwellers. Aim of the study is to identify the therapeutic uses of this plant in Sri Lanka. Ancient classical texts were used to collect data on Mee tree especially, Medicinal plants (Indigenous and Exotic) used in Ceylon. Articles were filtered through journals, magazines and newspapers. Databases such as Google scholar, Springer and Agroforestry were used to search journal articles. The journal articles from 2010-2022 were considered as eligible for this review. Search terms such as Madhuca longifolia, Mee tree, Medicinal uses were used to search journal articles. The final summary was formulated after a thorough reading of all above materials. As the results, the plant contains Vitamins, Ethylcinnamate, Amyrin acetates, Hexacosanol, Linoleic acid, Palmitic acid and many more chemical constituents. The Mee tree has analgesic, diuretic, tonic, aphrodisiac, astringent and demulcent properties with various parts of the plant. The parts are used in certain treatments in Ayurvedic medicine. The flowers, leaves, bark, roots, and seeds of the Mee tree are used to prepare medicines for rheumatism, bronchitis, headache, skin diseases, and worm infestations. The study was concluded as, this tree was so close and familiar to the lives of the people. This tree has many benefits for mankind, and many people have been interested in preserving it. However, due to the deforestation that has taken place in the country in the last few decades, the existence of Mee trees has been severely threatened. Today, Mee tree is a scarce resource in Sri Lanka. People should aware about protecting the plant for future generation. &#x0D; Keywords: Madhuca longifolia, Mee tree, Medicinal uses, Deforestation

An Insight into the Traditional Uses, Phytochemicals, and Pharmacological Properties of Polyalthia bullata King

Abstract: Polyalthia bullata King or Tongkat Ali Hitam, a term in the Malay language, encompasses a diverse group of plants belonging to different genera of the Annonaceae family. The native range of this species is Myanmar to Peninsula Malaysia, Borneo. It is a shrub or tree and grows primarily in the wet tropical biome. These plants have been utilized in Malaysia and Southeast Asia as an herbal aphrodisiac. The extracts of this plant have been reported to exert pharmacological activities, such as antioxidant, cytotoxicity, and aphrodisiac properties. The therapeutic properties of P. bullata are attributed to the presence of alkaloids and flavonoids. This study thoroughly analyzes the phytochemical and pharmacological research on P. bullata and its traditional medicinal properties. The review aims to provide a critical update on the scientific knowledge of P. bullata and to identify novel possibilities for investigating its therapeutic potential. There is limited scientific research on the phytochemical components and pharmaceutical application of P. bullata. To date, only a few compounds have been identified and isolated. There is a need for future studies to focus on the extraction technology, phytochemical profiling, and isolation of bioactive compounds from P. bullata to fill the research gap as well as to provide an important theoretical basis and valuable references for researchers and pave the way for the discovery and development of new and existing drugs.

Rekindling desire: Unveiling the Aphrodisiac potential of Apiaceae Elixirs

Background: In the realms of herbal pharmacology, the Apiaceae family has long held the torch, with parsley, coriander, and celery at the forefront. They have been extensively utilized in traditional therapies, including their use as aphrodisiacs. The primary objective of this study was to evaluate the aphrodisiac potential of three Apiaceae plants: Petroselinum crispum, Coriandrum sativum, and Apium graveolens, both individually and in combination, to substantiate their traditional medicinal usage. Methods: The administration of extracts orally (at a dose of 250 mg/kg of body weight) was carried out daily for 15 days in various groups of male rats. To induce receptivity in female rats used for mating, hormonal treatment was employed. The study encompassed the assessment of general mating behavior, which was compared to that induced by the standard reference drug, sildenafil citrate. Additionally, hematological and biochemical assays were conducted. Results: The results of this study demonstrated that oral administration of the extracts at a dose of 250 mg/kg significantly heightened sexual activity in male rats. This was characterized by a substantial increase in parameters such as mounting frequency, erection frequency, ejaculation frequency, and copulatory rate, coupled with a noteworthy reduction in mounting latency, intromission latency, and latency time. However, when compared to the positive control group (sildenafil), the polyherbal formulation did not induce significant alterations in hematological parameters such as red blood cell count, white blood cell count, blood platelet count, and hemoglobin levels. Furthermore, the hepatic and renal markers in treated rats displayed no significant disturbances when administered with the individual extracts of the three Apiaceae plants or in combination, in comparison to the control group. The results also unveiled a substantial augmentation effect in blood testosterone levels following the individual administration of Apiaceae plant extracts when compared to the positive control group. The combined administration of these extracts at a dose of 250 mg/kg exhibited an even more pronounced effect in enhancing testosterone levels than administering the individual extracts. Conclusions: In conclusion, the polyherbal formulation comprising these Apiaceae plants demonstrated a substantial and sustained enhancement in the sexual activity of healthy male rats, without any discernible adverse effects. This suggests that the formulation maintains aphrodisiac properties, possibly attributed to its nerve-stimulating effects, thereby enhancing libido and potency. These findings not only support the traditional use of these herbs for their aphrodisiac properties but also propose potential applications for human use as a natural alternative for addressing male sexual disorders and as aphrodisiac agents.

SHARBAT-E-MAWEEZ FOR IRON DEFICIENCY ANEMIA: A REVIEW

Anemia, characterized by reduced oxygen-carrying capacity in the blood, manifests through diminished red blood cell count or decreased hemoglobin levels. According to W.H.O. standards, hemoglobin levels below 13.0 gm/dl in adult males, below 12.0 gm/dl in non-pregnant adult females, and below 11.0 gm/dl in pregnant females signify anemia. Unani physicians often refer to this condition as Soo-Ul-Qiniya, exhibiting clinical signs such as weakness of the liver (Zauf-e-Kabid), nail brittleness (Zufr-e-Talqia), abnormal temperament (Fasad-e-Mizaj), pallor and yellowish discoloration of the skin (Zardi-wa-Sufaid Jild), and headaches (Sudaa). In numerous Unani medical texts, Sharbat-e-Maweez is recommended for treating iron deficiency anemia. It serves as a potent nutrient and hemopoietic agent, offering diverse benefits such as haemopoietic stimulation (mawalid-e-dam), aphrodisiac and general body toning properties (muqavvi-ebah-wa-badan), and liver strengthening effects (muqavvi-e-meda-wajigar). Sharbat-e-Maweez represents a palatable and easily administered form of Unani medication, thus enhancing patient compliance and efficacy in managing iron deficiency anemia.

A review on ecology, distribution, phytochemistry, and pharmacological properties of the medicinally important plant Pterocarpus santalinus L. (Red sanders)

Pterocarpus santalinus L., commonly known as Red sanders, belongs to the family Fabaceae. The plant is well-known for its distinctive wood, which has a stunning color, a delicate appearance, and exceptional technical features. The natural dye santalin, which is produced by the red wood, is used to color foodstuffs and pharmaceutical formulations. The decoction made from the heartwood is given numerous therapeutic characteristics in the ancient system of medicine. It has been used to induce vomiting as well as treat ulcers, mental disorders, and eye illnesses. It is known that the heartwood of Red sander trees has diaphoretic, aphrodisiac, anti-pyretic, anti-inflammatory, anti-helminthic, hemorrhage, and dysentery-preventing properties. Additionally, it has served as a cooling agent. It has been claimed that an ethanol extract of stem bark has anti-hyperglycemic properties. Various studies on the phytochemistry of stem bark extracts in ethanol extracts showed the presence of tannins, phenols, alkaloids, glycosides, flavonoids, and triterpenoids, as well as saponins. Isoflavone glucosides and two anti-tumor lignans, savinin, and calocedrin, are found in the heart wood. However, despite numerous claims of pharmacological activity, the species has not been thoroughly investigated. The current article emphasizes the phytochemistry, pharmacological potential, and applications of P. santalinus.

Mechanism of action of &lt;i&gt;Pterorhachis&lt;/i&gt; &lt;i&gt;zenkeri&lt;/i&gt; (Meliaceae), a sexual enhancer: effect on vas deferens contractility

Background: Pterorhachis. zenkeri commonly known as “Ayilalou” or “Démareur” is an aphrodisiac plant used by Cameroonian traditional healers to enhance libido and sperm production. This study was undertaken to investigate the aphrodisiac mechanism of P. zenkeri on the contractile activity of vas deferens with regard to its function on ejaculation. Materials and Methods: The proximal parts of rat vas deferens were mounted in a 20 mL organ bath containing Krebs solution at 37°C. Cumulative dose-response curves were recorded with KCl (35-280 mM), adrenaline (7-70 µM) and aqueous extract of P. zenkeri (3,55-21,3 mg/mL). Prazosin (type 1 alpha-adrenergic receptor antagonist, 10 µM), Nifedipine (a specific L-type calcium channel antagonist, 5 µM), 2-AminoethoxydiPhenyl Borate (2-APB, IP3 receptor antagonist, 200 μM) and calcium-free medium were further used to study the mechanism of action. Results: KCl, adrenaline and aqueous extract of P. zenkeri showed a concentration-dependent effect on vas deferens contractibility. Nifedipine and Pazosin partially inhibited the effects of P. zenkeri. In calcium-free medium containing Ethylene Glycol-bis (2-aminoethylether)-N,N,N’N’-tetraacetic acid (EGTA, 1µM), P. zenkeri triggered vas deferens contraction which was completely abolished in the presence of 2-APB. These results suggest that the aqueous extract of P. zenkeri possesses bioactive compounds capable of inducing vas deferens contractions through type 1 alpha adrenergic receptors and mobilization of extra and intracellular calcium. Conclusion: These results confirm the aphrodisiac properties of P. zenkeri through the activation of the emissive phase of ejaculation.