Medicinal Properties Research Articles

In vitro Cyclooxygenase inhibitory activity and GC-MS profiling of bioactive compounds in Bauhinia racemosa Lam.

Non-steroidal anti-inflammatory drugs (NSAIDs) are a common treatment for chronic pain and inflammation. While NSAIDs have been shown to reduce inflammation and pain associated with them, they have an array of side effects. Researchers investigated the COX inhibitory action of NSAIDs. They revealed that there are two distinct COX enzymes: COX-1 and COX2. Developing COX inhibitors has remained critical for producing innovative and safe anti-inflammatory drugs. Bauhinia racemosa Lam belonging to the family Fabaceae has a wide range of medicinal properties. The plant is used to treat various diseases in traditional medicine, but there is less knowledge based on clinical efficacy as an anti-inflammatory agent. In the present study Bauhinia racemosa Lam hydroalcoholic extract were screened for COX inhibition and GC-MS analysis was done to screen phytochemicals. The results obtained were found to inhibit 89% of COX activity significantly as compared to standard drug (Diclofenac sodium). GC-MS analysis revealed a total of ten potent bioactive compounds. The samples were identified by comparing retention time and peak area to literature and interpreting mass spectra. Results observed from the study suggest that the hydroalcoholic extract of Bauhinia racemosa Lam possess anti-inflammatory activity and can be utilized as an alternate source for NSAIDs. Keywords: COX, Bauhinia racemosa Lam, Anti-inflammatory, NSAIDs.

Ethnomedicinal and Phytopharmacological Aspects of Vernonia amygdalina (Bitter Leaf) Utilized as a Traditional Medicinal Herb

Vernonia amygdalina Delile, commonly known as “bitter leaf,” is a shrub in the Asteraceae family, widely seen in tropical regions of Africa. Vernonia amygdalina is found to be traditionally used in African medicine. Various parts of this plant, especially the leaves, are utilized to treat ailments such as fever, diabetes, and gastrointestinal issues. Research from multiple researchers has shown a wide range of phytochemical and bioactive compounds present in Vernonia amygdalina; examples are terpenoids, tannins, alkaloids, saponins, flavonoids, steroids, glycosides, etc., which have contributed to the medicinal properties of Vernonia amygdalina. Vernonia amygdalina has shown its therapeutic and remedial potentials due to the presence of phytochemicals which exhibit effects such as anti-microbial, anti-inflammatory, anti-cancer, anti-oxidant, anti-diabetic, anti-hyperglycemic, anti-diarrheal, anti-helminthic, anti-pyretic, and anti-nociceptive effects. In this article, the authors highlight recent progress in using Vernonia amygdalina and its therapeutic effects. Research, review, and case study articles were used to write this review. The articles were obtained from academic websites such as Research Gate, Google Scholar, the National Library of Medicine, African journals online, and Semantic journals, and some articles were obtained through a simple Google search. Articles that discussed the medicinal, ethanopharmacological, and therapeutic properties of Vernonia amygdalina were selected for the review. Search terms such as “Vernonia amygdalina,” “bitter leaf,” “phytochemical properties,” and “therapeutic effects” were used to search for relevant articles on the academic databases. Boolean operators such as “AND” and “OR” were used to refine the search further and ensure a comprehensive selection of articles.

Immunoexpression of CD34, CD68 and CD3 in Cadmium-Induced Liver Damage and Protective Effectiveness of Bee Bread (Perga)

Cadmium (Cd) is one of the potent environmental toxicants that causes oxidative stress in many organs of the body, including the liver. Perga (bee bread) is used for apitherapeutic purposes due to its medicinal properties. This study was conducted to investigate the effectiveness of perga on endothelial damage and inflammatory cell activation in the liver as a result of exposure to Cd. For this purpose, 32 male Wistar rats (8 rats/group) were randomly divided into 4 groups, as the control, perga (0.5 g/kg of perga), Cd (5 mg/kg of CdCl2), and Cd + perga (0.5 g/kg of perga + 5 mg/kg of CdCl2) groups. Daily intragastric Cd and/or perga was administered for 4 weeks. At the end of the study, the rats were euthanized and liver tissue sections were taken and stained with hematoxylin-eosin and Masson’s Trichrome. Immunohistochemically, the reactivity of the liver sinusoidal endothelium was determined using CD34, the reactivity of the Kupffer cells was determined using CD68, and the levels of T-lymphocyte cells were determined using CD3 antibodies. Exposure to Cd caused significant histological changes in the liver. Immunohistochemically, exposure to Cd caused an increase in the expressions of CD34, CD68, and CD3. On the other hand, the cotreatment of Cd and perga caused partial improvement in some histopathological changes. Compared to the Cd group, there was a decrease in CD34 and CD68 positivity in the Cd + perga group, while no significant difference was detected in the number of CD3-positive cells between the groups. The results revealed that the histopathological changes and inflammation in the rat liver could partially improve with perga supplementation.

Olax dissitiflora Oliv. (small-fruited olax): Current status and future prospects as medicinal plant

Olax dissitiflora Oliv. (O. dissitiflora) has several medicinal uses, some of them known since prehistoric times. The present review compiles existing knowledge of the chemical and pharmacological properties, current medicinal uses, and further use potential and applications of O. dissitiflora. Multiple searches on existing literature on the medicinal, phytochemistry and pharmacological properties of O. dissitiflora were conducted in online databases such as Scopus, JSTOR, PubMed, Google Scholar and Science Direct as well as using pre-electronic literature sources obtained from the university library. This study showed that the bark, leaves, roots and twigs of O. dissitiflora are used as aphrodisiac, emetic, mosquito repellent and purgative, and as traditional medicines against dental problems, gonorrhoea, hernia, venereal diseases and wounds. The phytochemical evaluation of the plant revealed that it contains reducing sugars, alkaloids, flavonoids, phenolic compounds, quinones, saponins, steroids, tannins, terpenoids, 21-epimachaerinic acid, oleanolic acid, hederagenin, oleanolic acid 3-O-glucuronide, amphotericin, santalbic acid, exocarpic acid and octadic-9,11-diynoic acid. The pharmacological assessments showed that the crude extracts and phytochemical compounds isolated from the species have antibacterial, antifungal, antiplasmodial, larvicidal and adulticidal activities. The collected ethnomedicinal and ethnopharmacological properties of O. dissitiflora documented in this review will assist to understand the therapeutic relevance and potential of the species as well as providing baseline data required for ethnopharmacological assessments required in the discovery of novel plant-based health products. There is also need for more studies focusing on phytochemistry, pharmacological properties and toxicological evaluations, in vivo and clinical research on O. dissitiflora to compliment and validate the ethnomedicinal properties of the species.

Influence of Green Synthesized Silver and Zinc Nanoparticle on Seed Quality Attributes in Red Sander (Pterocarpus santalinus Linn.)

Red Sanders (Pterocarpus santalinus), or Rakta chandana, is an endangered tree native to the Southern Indian Peninsula, valued for its medicinal and dye properties. However, its germination is hindered by a hard seed coat, phenolic compounds and hormonal imbalances. Nanotechnology in forestry enhances product innovation, paper processes and sustainability through plant-based nanoparticle biosynthesis. The experiment used a completely randomized design (CRD) with three replications and evaluated seven presowing treatments: T1 (AgNPs at 1000 ppm for 24 hours), T2 (ZnNPs at 2000 ppm for 24 hours), T3 (Conc. H2SO4 for 12 minutes), T4 (NaDC 500 ppm), T5 (Dewinging), T6 (soaking in hot water at 100°C for 5 minutes) and T7 (control). The results indicated that seeds treated with ZnNPs at 2000 ppm (T2) exhibited highest germination rate (56%), germination speed (1.04), root length (17.05 cm), shoot length (16.33cm) and highest dry weight (6.22 g) and highest seedling vigour Index-I (1869). In comparison H2SO4 treatment (T3) delivered 51.67 per cent germination and a speed of germination (0.95), with root length (15.28 cm), shoot length (16.22 cm), dry weight (5.24 g) and seedling vigour Index (1628) slightly lower but still significant. The control (T7) had the lowest performance with 31 per cent germination, a speed of 0.36, root length (15.28 cm), shoot length (16.22 cm), lower dry weight (1.63 g) and the lowest Seedling Vigour Index (649). Overall, ZnNPs at 2000 ppm (T2) were the most effective in enhancing germination, seedling growth and overall vigour in Red sanders.

Novel characterisation of Curvularia geniculata associated with leaf blight on Costus igneus in India

Costus igneus Nak, commonly referred as insulin plant or spiral flag, is a perennial herb belonging to the family Costaceae. Owing to its ability to regulate the blood sugar level, it is considered as a boon plant for diabetic patients, hence popularly known as the “sugar plant”. Although few foliar diseases have been documented on C. igneus, they generally occur in minor frequency under Indian conditions. However, in May 2022, a moderate to severe incidence of leaf blight was observed on insulin plants at University of Agricultural Sciences, GKVK, Bangalore, and nearby medicinal gardens. The affected leaves exhibited light brown lesions coalesced to form papery blight, gradually leading to complete drying of leaves. The current study aimed to identify, characterize, and document the fungal pathogen responsible for the disease, with a focus on its morphological, molecular, and biological characteristics to ensure accurate identification. Additionally, the study sought to determine optimal conditions for pathogen growth and sporulation to support the development of effective disease management strategies. The associated fungus was isolated, purified and identified as Curvularia geniculata through morphological and multigene phylogenetic analysis, using internal transcribed spacer (ITS) and large sub unit (LSU) regions of rDNA, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene. Biological characterization revealed that cornmeal agar (CMA) at 30 °C and pH of 7 were ideal for better growth and abundant sporulation. These findings, highlighting the emergence of C. geniculata as a novel fungal pathogen infecting C. igneus in India, are crucial for developing effective disease management strategies to safeguard the medicinal properties of the plant.

Effect of Plant Growth Regulators on Germination and Seedling Growth of Passiflora alata and Passiflora edulis

The yellow (Passiflora edulis) and sweet (Passiflora alata) passion fruit plants hold significant economic importance in tropical fruit cultivation, valued not only for the quality of their fruit but also for their medicinal properties. Conventional propagation through seeds faces challenges due to irregular and slow germination, affecting the time required for seedling formation and the viability and uniformity of plantations. The use of plant growth regulators has been explored as a strategy to overcome these barriers, improving both the rate and uniformity of seed germination. This study aimed to evaluate the influence of seed imbibition with plant growth regulators on the germination and subsequent growth of yellow and sweet passion fruit seedlings. Gibberellic acid (GA3) and GA4+7 combined with 6-benzyladenine (GA4+7+6BA) were applied in five different concentrations (0, 250, 500, 750, and 1000 mg L−1 a.i.). The experiments were conducted in both laboratory and greenhouse conditions, following a completely randomized design with a 2 × 5 factorial scheme. The varieties tested were ‘BRS Mel do Cerrado’ for sweet passion fruit and ‘IAC-275’ for yellow passion fruit. Quantitative parameters, such as germination percentage, germination speed index, fresh and dry biomass of roots and shoots, and enzymatic activity, were assessed. The results indicated that GA3, at higher concentrations, significantly enhanced both germination percentage and speed index in both Passiflora alata and Passiflora edulis when compared to the control. Additionally, seedlings treated with GA3 showed a marked increase in shoot and root biomass, particularly at concentrations of 500 and 750 mg L−1. Enzymatic assays revealed heightened catalase and peroxidase activities in treated seedlings, indicating improved stress tolerance. In contrast, the GA4+7+6BA treatment showed less pronounced effects on seedling growth. Overall, GA3 was more effective in enhancing germination and seedling growth in both species, suggesting its potential application in improving the propagation of passion fruit.

Fertility and teratogenic study of the aqueous extract of Hibiscus sabdariffa L. in female Sprague Dawley rats

Hibiscus sabdariffa (roselle) has long been gaining attention in phytotherapy research due to its medicinal properties. Despite its benefits, there is very scarce information available on the reproductive toxicity of this plant. The aqueous extract of H. sabdariffa (AEHS) was tested in the present study to investigate its potential effects on fertility and teratogenicity in 40 female Sprague Dawley rats. AESH treatment was administered orally by gavage at four different dosages: 250, 500 and 1000 mg/kg/day or distilled water (control). Treatment began from pre-mating and continued through mating up to the 19th day of pregnancy periods. Throughout this study, the reproductive parameters were evaluated until the day of sacrifice (day 20th of pregnancy). Results obtained revealed no significant differences in general physical health, behaviours and maternal body weights throughout the treatment period. Furthermore, the mean length of the oestrous cycle was not statistically affected, even though a few rats displayed irregular cycles. In addition, there was no statistical significance in the mating and pregnancy indices, number of corpora lutea and implantation sites, percentages of pre-implantation loss and postimplantation death and reproductive organ weights. Foetal parameters such as the number of live foetuses, sex ratio and body weight were also not statistically affected by AESH. Ultimately, there were no signs of teratogenicity observed since none of the foetuses exhibited congenital malformations. In conclusion, these findings imply that the oral administration of AEHS up to 1000 mg/kg/day did not pose any significant toxicity on the fertility and teratogenicity but slightly affected the oestrous cycle in rats.

Research Progress on the Mechanism for Improving Glucose and Lipid Metabolism Disorders Using Phenolic Acid Components from Medicinal and Edible Homologous Plants.

Glucose and lipid metabolism disorders are the core pathological mechanism of a variety of metabolic diseases, and the incidence of related diseases is increasing year by year, which seriously threatens human life and health. Traditional Chinese medicine with medicinal and edible properties refers to Chinese medicinal resources that have both medicinal and edible characteristics. Due to its safety and its health-promoting and medicinal functions, traditional Chinese medicine has received increasing attention in the development of functional health foods. Phenolic acids are important secondary metabolites that are ubiquitous in medicinal and edible homologous plants, and the regulation of glycolipid metabolism is an important activity and plays a key role in many diseases. In this paper, we focus on the alleviation of glycolipid disorders using MEHH phenolic acids, which regulate glucose metabolism and lipid metabolism, improve insulin resistance, inhibit inflammatory responses, alleviate oxidative stress, and regulate intestinal flora; additionally, we summarize the mechanism in order to provide a reference for MEHH phenolic acids in the treatment of glycolipid metabolism diseases.

The Medicinal Properties of Anogeissus leiocarpus (African Birch Tree) and the Development of a Drug for Diabetes Mellitus and its Complications: A Review

The Medicinal Properties of Anogeissus leiocarpus (African Birch Tree) and the Development of a Drug for Diabetes Mellitus and its Complications: A Review

Prophylactic Antihypertensive Effect of Extract of Simarouba glauca on Salt-Load Induced Hypertension in Normotensive Male Wistar Rat

Simarouba glauca has been reported to demonstrate a wide range of medicinal properties; including folklore management of hypertension disorder. The current study focused on the application of aqueous leaf extract of Simarouba glauca (AESG) as a potential prophylactic anti-hypertensive agent in male Wistar rats, following salt-load induced hypertension. A total of 15 experimental adult male Wistar rats weighing between 184 and 244 g were used for the study. The rats were allotted into five (5) groups of 25, 50, and 100 mgkg-1 body weight AESG; group that received 8 % NaCl for one week to induce hypertension; replaced with 0.9 % NaCl daily in drinking water for 4 weeks; the normotensive group, received food and water only ad libitum. Body weights and relevant hemodynamics were obtained weekly for four weeks, using the non-invasive (tail-cuff) MRBP system according to the method described by Bunag and Butterfield. Biochemical evaluation and histopathology investigation were conducted on blood plasma and relevant tissues respectively after 4 weeks according to previously established and reported methods; data were analyzed with GraphPad Prism, version 9 and presented as mean ± Standard Deviation. The results indicated that salt-load elicited significant weight loss; elevated hemodynamics; particularly, systolic and diastolic blood pressures; altered relevant biochemical indicators of hepatic and renal functions. Inversely, groups pre-treated with respective dose of AESG exponentially gained weight, significantly prevented alterations of hemodynamics and mitigated relevant biochemical indicators and pathological changes in relevant organs. Pre-treatment with AESG; particularly at 50 mgkg-1, remarkably demonstrated significant anti-hypertensive potential.

Mushroom alkaloids as nutraceuticals, bioactive and medicinal properties: a preliminary review

Mushroom alkaloids are quite interesting due to their distinct secondary metabolites. Alkaloids are a class of secondary metabolites that are found in different types of organisms. The primary focus of this study is the alkaloids that were taken out of the mushrooms. Mainly the mushrooms alkaloids are classified as 2 groups like indoles and isoxazoles. In the present paper 68 distinct alkaloids produced from mushrooms were attempted to be listed under 24 distinct groups; i.e. 24 alkaloids were kept under Indole group, 5 different alkaloids were kept under ? - carboline group and pyrroloquinoline group, 4 different alkaloids were kept under pyrrole group, and 3 different alkaloids were mentioned under quinoline groups. Mushrooms were used as food in many parts of the world. The alkaloids obtained from mushrooms showing different bioactivities like antimicrobial, anticancer, anti-diabetic, hepatoprotective, anti-inflammatory, antioxidant, immunomodulatory, anti-obesity, anti - ageing, nematicidal, helmintic, against cardiovascular disease and as antiasthmatic agent. Mushrooms were widely used in the traditional medicine of many countries like china, India, Taiwan, Japan etc. these mushrooms became great resources for many groups of alkaloids with bioactivities which should be useful in present day modern clinical and pharmacological research. The present review aims at listing the applications of mushroom alkaloids in different fields like medicine, health science, pharmacy etc.

Polyphenolic Profile and In vitro, In Silico Study of Stem Extracts from J. Maritimus (Juncaceae) Harvested from Eastern Algeria as Potential Anti-Inflammatory and Antioxidant Agents.

Juncus maritimusan extremophilous microorganism speciesknown for its medicinal properties was collected in the Biskra region with the aim of its valorization. The volume size of polyphenols, flavonoids and condensed tannins was performed using the Folin-Ciocalteu method, aluminum trichloride and vanillin respectively. The volume of Polyphenols was 127.73±0.20 μg EAG/mg ES, the volume offlavonoids was 16.42±0.42 μg EQ/mg ES, and the volume ofcondensed tannins was 10.10±0.35 μg EC/mg ES. The results of the antioxidant activity tests using the DPPH and ABTS methods reveal that the ethyl acetate extract had the highest activity in both tests. The results of the in vitro anti-inflammatory activity, using the BSA protein denaturation assay, showed that the percentage of denaturation inhibition wasproportional to the concentration of the extract. At a concentration of 5 mg/mL, the inhibition percentage of the extract were 82.03 % and 80.23 %, respectively,which wereclose tothose of theanti-inflammatory drug Diclofenac.Furthermore, molecular docking simulations indicated that Berberine has high binding affinity to the targets COX-2 and PLA-2 In fact,bioisosteric replacement is being usedto discover new analogs of Berberine. Finally, ADME-Tox predictions demonstrated that this compound and its analogs were not hepatotoxic. This result may lead to the selection ofBerberine and its analogs as active compounds with anti-inflammatory and antioxidant effects.

Synthesis, in vitro antibacterial and antioxidant evaluation, DFT calculation, molecular docking, and ADMET studies of novel N-Acyl-6-chloro-2(3H)-benzoxazolone derivatives

A new series of N-acyl-6-Chloro-2(3H)-benzoxazolone derivatives (4a-4g) were synthesized using an eco-friendly catalyst. The compounds were characterized using spectroscopic techniques, including FTIR, 1H NMR, 13C NMR, and GC–MS. Their antimicrobial activity against various bacterial strains, including both Gram-negative and Gram-positive bacteria, was evaluated and yielded promising results. The synthesized compounds were also tested for their antioxidant properties using the DPPH radical-scavenging method, where compound 4f exhibited the highest activity with an IC50 of 1.54 μg/mL, surpassing that of ascorbic acid (IC50 = 1.7 μg/mL). Additionally, DFT calculations were performed to investigate the compounds’ chemical reactivity, including the analysis of HOMO and LUMO frontier molecular orbitals, global reactivity descriptors, and molecular electrostatic potential. Molecular docking studies were conducted to explore the interactions between the synthesized compounds (4a-4g) and the standard drug ciprofloxacin at the active site of DNA gyrase. Furthermore, physicochemical properties, lipophilicity, water solubility, pharmacokinetics, drug-likeness, and medicinal chemistry properties were estimated using SwissADME. Toxicological profiles, including hepatotoxicity, carcinogenicity, immunotoxicity, mutagenicity, cytotoxicity, and LD50, were predicted using the ProTox-III web tool. The findings suggest potential therapeutic applications for combating bacterial strains, indicating that these synthesized compounds could serve as lead compounds for antibiotic drug development.

Chemical analysis of Alliin-Rich Allium sativum (Garlic) extract and its safety evaluation in Drosophila melanogaster

Garlic (Allium sativum) has been traditionally valued for its medicinal properties attributed to the presence of organosulfur compounds. Despite its benefits, concerns about herbal extract toxicity have arisen, necessitating safety assessment. This study was designed to evaluate the chemical analysis and safety profile of Alliin-Rich Garlic Extract (ARGE) using Drosophila melanogaster as a model organism. The ARGE was extracted from garlic cloves (Allium sativum Linn: UIH-23262) using a microwave-assisted method and characterized using UPLC-ESI-MS, 1H NMR, HPLC and IR. Its safety evaluation was determined using D. melanogaster (Harwich strain), and various assays were conducted on 1–3-day-old flies. Toxicological markers and oxidative stress were assessed to understand the impact of ARGE on the flies. Chemical profiling of ARGE using UPLC-ESI-MS, confirmed the presence of alliin (S-ally-L-cysteine-S-oxide), L-arginine, γ-glutamylmethionine, S-(2-carboxypropyl) glutathione, N-γ-glutamyl-S-(1-propenyl) cysteine, N-γ-glutamyl-S-(2-propenyl) cysteine, N-γ-glutamylphenylalanine, S-(allylthio) cysteine, γ-glutamyl-S-allylthiocysteine and eruboside B. HPLC confirmed an alliin content of 0.073 mg/g. Toxicological assessment in D. melanogaster revealed that ARGE enhanced antioxidant defenses by increasing total thiol levels and GST activity, while reducing acetylcholinesterase activity. No significant alteration was observed in catalase activity and cellular metabolic rate. Histological examination revealed no alterations in the histoarchitecture of the brain, fat body or gut of D. melanogaster. The study demonstrated the safety of ARGE in D. melanogaster, supporting its potential as a safe herbal remedy.

Antioxidant and immunomodulatory activities of ethanol extracts from Syzygium cumini L. Skeels and Pogostemon cablin Benth

Syzygium cumini and Pogostemon cablin are mostly cultivated in tropical climates for culinary and perfumery purposes, yet their potential medicinal properties remain underreported. The aim of this study was to examine the antioxidant and immunomodulatory activities of ethanol extracts from S. cumini (EESC) and P. cablin (EEPC). Reflux extraction was carried out using 96% ethanol on the collected plant specimens to produce EESC and EEPC. Secondary metabolites of each extract were identified using gas chromatography-mass spectrometry (GC-MS). The extracts were measured for total phenol and flavonoid levels and 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity. The immunomodulatory activity test was carried out in vivo by assessing several parameters, including the phagocytic index via the carbon clearance method, organ indices, antibody titers, and delayed-type hypersensitivity (DTH) response, using sheep red blood cells (SRBC) as antigens. The extracts were also examined for their anti-inflammatory activity in acute and chronic inflammation models. In the DPPH antioxidant test, EESC and EEPC had IC50 values of 12.33 µg/mL and 182.17 µg/mL, respectively. Both extracts showed immunosuppressant activity, marked by a phagocytic index of <1. EESC yielded lower organ indices for the liver (p=0.025 at 200 mg/kg BW), spleen (p=0.028 at 100 mg/kg BW), and thymus (p=0.032 at 200 mg/kg BW) compared to the control group. For EEPC, lower organ indices were observed in the liver at 100 mg/kg BW (p=0.005) and 200 mg/kg BW (p=0.031). In the primary antibody titer and DTH tests, both EESC and EEPC showed immunosuppressant activity at 200 and 400 mg/kg BW (p<0.05). The extracts suppressed both the innate and adaptive immune systems. Both EEPC (p=0.004) and EESC at 100 mg/kg BW (p=0.03) significantly reduced serum TNF-α levels. In conclusion, EESC and EEPC have the potential as immunosuppressive and anti-inflammatory agents.

Integrated Transcriptomics and Metabolomics Studies Reveal Steroid Biosynthesis Pathway and BCL2 Inhibitory Diazo-Progesterone of Drimia indica for Conservation and Sustainable Utilization.

This study is the first report on the sequence of the transcriptome of Drimia indica, a non-model plant with medicinal properties found in a forest tribal belt, using the Illumina NovaSeq platform. The primary objectives of this study were to elucidate the gene expression profiles in different tissues, identify key regulatory genes and pathways involved in secondary metabolite biosynthesis, and explore the plant's potential pharmacological properties. The study generated 670087 unigenes from both leaves and roots and identified putative homologs of annotated sequences against UniProt/Swiss-Prot and KEGG databases. The functional annotation of the identified unigenes revealed the secondary metabolite biosynthetic process as the most prominent pathway, with gene enrichment analysis predominantly accounting for secondary metabolite pathways, such as terpenoid, steroid, flavonoid, alkaloid, selenocompound, and cortisol synthesis. The study also identified regulatory genes NAC, Bhlh, WRKY, and C2H2 on the transcriptome dataset. The functionally annotated unigenes suggested phytocompounds in Drimia indica to have multi-potent properties, such as anti-cancer, anti-inflammatory, and anti-diabetic activities, which has been further validated by GC-MS-based metabolite profiling. Notably, we have identified two novel molecules, di-azo progesterone and 4H-pyran-4-one 2,3-dihydro-3,5-dihydroxy- 6-methyl, with potential BCL2 inhibitory anticancer properties, supported by stable binding interactions observed in molecular docking and dynamics simulations. Additionally, an abundance of mono-nucleotide SSR markers has been identified, useful for genetic diversity studies. This study provides a foundational understanding of the molecular mechanisms in Drimia indica, highlighting its potential as a source for novel therapeutic agents and contributing valuable insights for future pharmacological and agricultural applications. However, further in vivo studies are warranted to confirm these findings and validate their pharmacological efficacy and therapeutic potential. The SSR markers identified also offer valuable tools for molecular genetics, plant breeding, and sustainable drug development.

Comprehensive Review on Nilofar (Nymphaea alba Linn): Unani Perspectives and Therapeutic Potentials

Nilofar (Nymphaea alba Linn) is commonly known as the white-water lily. It is a hydrophyte with enormous medicinal properties, renowned for its alluring white flowers. It is distributed worldwide in ponds, lakes, and marshy areas. Its various parts have been extensively utilized in Unani medicine globally, particularly in the Indian subcontinent, to prevent and treat a variety of ailments. Numerous research findings have documented its therapeutic effects, including anti-inflammatory, anti-hepatitis C, anti-diarrheal, hepatoprotective, antibacterial, anticarcinogenic, antiurolithiatic, uterotonic, anxiolytic, antidepressant, CNS depressant, anticonvulsant, antihyperlipidemic, and antioxidant activities. In Unani medicine, Nilofar is used to treat various illnesses such as palpitations, diarrhea, hepatotoxicity, inflammation, migraines, anxiety, depression, and convulsions. Nilofar contains a variety of chemical constituents, including alkaloids, tannins, flavonoids, phenolic content, glycosides, aglycons, phenolic acids, cardiac glycoside nymphalin, and others. This review explores the therapeutic potential of Nilofar, shedding light on its pharmacological properties, traditional uses, and emerging research. By combining traditional knowledge with the latest scientific findings, this review aims to encourage further research and facilitate its integration into mainstream healthcare practices.

Exploring Phytochemical Profile and Biological Activities of Callistemon viminalis (Sol. ex Gaertn.) G.Don ex Loudon) By In vitro and In silico Approaches.

Callistemon viminalis (Sol. ex Gaertn.) G.Don ex Loudon) (family: Myrtaceae) is used for its medicinal properties in treating various metabolic disorders. We investigated the chemical characterization and biological screening of the n-hexane extract of C. viminalis. The total phenolic content was (37.45±7.40 mg GA.E/g D.E±S.D) and the total flavonoid content was (18.43±6.34 mg R.E/g D.E±S.D). GC-MS screening of the n-hexane extract tentatively identified 70 bioactive phytochemicals. The maximum antioxidant potential (289.99±9.01 mg T.E/g D.E±S.D) was observed via the FRAP assay. Enzyme inhibition assays revealed that n-hexane extract of C. viminalis showed enzyme inhibition against the enzymes including α-glucosidase (6.9±0.13 mmol of ACA.E/g D.E±S.D); α-amylase (7.2±0.56 mmol of ACA.E/g D.E±S.D), urease (4.95±0.9 mg of TU.E/g D.E±S.D), acetylcholinesterase (2.9±0.08 mg GALA.E/g D.E±S.D), lipoxygenase (4.93±1.05 mg of Indo.E/g D.E±S.D) and tyrosinase (4.33±0.62 mg of KA.E/g D.E±S.D). The extract showed maximum antibacterial activity against Staphylococcus aureus (71.30±4.44 %) followed by Bacillus subtilis (68.55±2.70 %), Pseudomonas aeruginosa (57.86±6.02 %), and Salmonella typhi (53.90±5.05 %). Docking studies revealed good docking interactions between ligands and the studied enzymes, whereas ADME analysis revealed the pharmacokinetic profiles of the phytoconstituents. C. viminalis possesses promising therapeutic potential and can be further explored for drug development and drug design.

Acceptability of Moringa oleifera seeds flour supplement-added to normal diet by Women Living With Human Immunodeficiency Virus (PLWHIV) in resource-limited setting

This article aims to assess the acceptability of Moringa oleifera seed supplementation among HIV-positive women in resource-limited settings. The management of HIV/AIDS in resource-constrained settings presents numerous challenges, highlighting the need for affordable supplements to complement standard anti-retroviral therapy (ART). Moringa oleifera, known for its nutritional and medicinal properties, has been noted for its immunomodulatory, anti-inflammatory, and antiviral effects. A descriptive study utilising a Likert-scale survey evaluated participants' familiarity with Moringa oleifera, perceived health benefits, potential risks, ease of dietary integration, and taste acceptability. The findings revealed a generally positive acceptance of Moringa oleifera supplementation, with a mean acceptability score of 2.5750. Notably, 58.2 per cent of participants found the taste palatable, and 72.2 per cent reported ease of incorporation into their daily diet. A significant 90 per cent expressed willingness to use Moringa oleifera if proven effective in suppressing HIV viral load. The study also highlighted the influence of healthcare provider recommendations, with 77.7 per cent of participants more likely to use Moringa oleifera based on professional advice. In conclusion, Moringa oleifera seed supplementation is generally acceptable among People Living with HIV, particularly when supported by healthcare providers. To enhance its use, the study recommends increasing awareness, engaging healthcare professionals, and conducting further research to maximise its potential health benefits for HIV-positive individuals.