Ivms Krishnarao Bhegade Institute Of Pharmaceutical Education And Research, Talegaon Dabhade, Pune. Maharastra- 410507.
This review highlights the significant therapeutic potential of Dalbergia sissoo, Curcuma longa, and Moringa oleifera, but also emphasizes the need for extensive future research to fully realize and validate their medicinal benefits. Although current laboratory, animal, and limited clinical studies provide promising evidence of their diverse pharmacological activities—including anti-inflammatory, antioxidant, antimicrobial, antidiabetic, neuroprotective, reproductive, osteogenic, and anticancer effects comprehensive mechanistic studies remain incomplete. Future research should focus on elucidating the precise molecular pathways and bioactive compounds responsible for these effects to better understand how these plants interact with human physiology. Moreover, there is a strong need to standardize extraction processes, phytochemical characterization, and dosage regimens, which are essential for reproducibility and safety assessment. Large-scale, well-designed clinical trials are urgently required to establish efficacy, optimal doses, pharmacokinetics, and long-term safety in diverse patient populations. Such studies will help overcome current gaps related to clinical validation and provide a scientific basis for integrating these plants into mainstream healthcare. Additionally, future investigations could explore synergistic effects when combining these plants or their extracts with conventional drugs, potentially enhancing therapeutic outcomes or reducing side effects. Research on formulation strategies to improve bioavailability, especially for compounds like curcumin that have poor absorption, will also be critical. While the existing literature strongly supports the therapeutic promise of Shisham, Turmeric, and Moringa oleifera, future work must prioritize rigorous experimental and clinical research to translate these findings into validated, safe, and standardized therapies that can be widely recommended and adopted in evidence-based medicine.
Dalbergia sissoo:
Dalbergia sissoo, commonly referred to as shisham, has been scientifically established to possess robust anti-inflammatory capabilities, a conclusion supported by multiple research findings. Investigations using animal models have demonstrated that ethanolic extracts derived from both its leaves and its stem bark exhibit a significant capacity to diminish inflammatory responses, effectively inhibiting specific manifestations such as edema (swelling) and the development of granulomas. Importantly, these therapeutic effects were achieved without inducing any harmful damage to gastric tissues, indicating a favorable safety profile in this regard. [1,2] The mechanism behind this potent anti-inflammatory action is credited to the plant's abundant and diverse array of phytochemical constituents, which include flavonoids, tannins, saponins, glycosides, and terpenoids. Collectively, these bioactive compounds mediate their effects by stabilizing cellular membranes and exerting an inhibitory influence on critical inflammatory processes, including the denaturation of proteins and the increased permeability of blood vessels. This compelling pharmacological profile not only makes shisham a valuable agent for alleviating a wide spectrum of inflammatory conditions but also substantiates its long-standing traditional application for treating specific disorders such as arthritis, rheumatic pain, and various skin diseases [3].
Fig.No.(1) Shisham leaves
Turmeric:
Turmeric the vivid yellow spice derived from the root of the Curcuma longa plant, is celebrated not only for its bright color but also for its extensive health benefits. This remarkable spice has been used for centuries both as a flavorful ingredient in cooking and as a natural remedy in traditional medicine. The primary bioactive substance in turmeric, curcumin, has garnered considerable attention in scientific research due to its promising health-promoting properties. Curcumin is especially recognized for its strong anti-inflammatory and antioxidant effects, which have spurred numerous studies investigating its potential as a treatment for various inflammation-related health conditions. [4] Inflammation is a natural defense mechanism of the immune system that responds to external threats such as pathogens. However, excessive or uncontrolled inflammation can cause immune cell death and immune system dysfunction, potentially leading to chronic degenerative diseases and cancer.[5]
Fig.No. (2) Turmeric powder
Moringa:
While steroids and NSAIDs such as azathioprine and aspirin—are traditionally used to manage acute and chronic inflammatory conditions, their long-term use is associated with a range of harmful side effects. As a result, there is growing scientific and public interest in developing natural anti-inflammatory agents that offer better safety and effectiveness. Alongside this, as standards of living rise, people increasingly prefer natural functional foods with anti-inflammatory benefits. Gamma-aminobutyric acid (GABA) is a non-protein amino acid naturally found in plants, bacteria, and animals. In mammals, it serves as a key inhibitory neurotransmitter in the central nervous system and contributes to several physiological processes, including playing an important role in the body’s anti-inflammatory responses.[6]
Fig.no.(3) Moringa leaves.
HISTORY: -
Dalbergia sissoo, commonly known as shisham or North Indian rosewood, is native to the Indian subcontinent and parts of southern Iran, especially flourishing in the sub-Himalayan region of India and Pakistan. It naturally grows along riverbeds, water channels, and alluvial flats prone to annual floods, with a native range extending from the Indus River in Pakistan through India to Assam, and possibly earlier introductions in areas from Oman to Burma and southern India. It thrives in tropical dry deciduous forests and typically colonizes newly formed lands like hillsides and roadsides with exposed mineral soil. Beyond its natural range, it has been widely planted across South Asia and other parts of the world for timber, shade, erosion control, and windbreaks since at least the early 20th century.?[7,8]
Historically, Dalbergia sissoo has held significant importance for its durable, strong, and decay-resistant timber, highly valued in South Asia for furniture, cabinetry, boat building, and construction. Its timber was praised in 12th-century Persian manuscripts associated with Mughal gardens, and colonial botanists in the 19th century cataloged it as Dalbergia sissoo, noting its resinous wood closely resembling Brazilian rosewood. The tree’s wood was also used traditionally for fuel and charcoal due to its high calorific value.?[,9,10]
Medicinally, the tree has deep roots in Ayurvedic and traditional South Asian systems. Ancient Ayurvedic texts such as the Sushruta Samhita and Charaka Samhita mention “Simsapa” (shisham) for arthritis relief and wound healing. Folk healers in rural Punjab and Sindh used bark pastes for sprains and fractures, referring to the tree’s golden sap as “Zarsund.” In Nepal and Southeast Asia, leaves and bark have been used to treat skin infections, dysentery, and other ailments. The tree’s heartwood, bark, leaves, and seed oil have diverse applications including anti-inflammatory, antipyretic, antimicrobial, hepatoprotective, and immunomodulatory effects. Modern phytochemical studies since the 1990s have revived and validated many traditional uses, and today’s Ayurvedic formulations often incorporate standardized extracts of shisham for joint health and rejuvenation.?[11,12]
In addition to timber and medicinal uses, slender twigs of Dalbergia sissoo have traditionally functioned as natural toothbrushes ("datun"), a practice enduring in rural South Asia. The tree also serves ecological functions like soil stabilization along riverbanks and soil fertility enhancement through nitrogen fixation in agroforestry systems. [?9]
In summary, Dalbergia sissoo's historical background encompasses its origin in the sub-Himalayan region, longstanding cultural and medicinal uses in South Asia, and extensive planting worldwide. It bridges ancient Ayurvedic wisdom and modern applications, with a legacy as a multipurpose tree valued for timber, traditional medicine, ecological services, and cultural practices. [9 ,12]
Dalbergia sissoo (shisham) offers many benefits: its leaves serve as nutritious fodder for livestock, while its root, bark, and leaves have traditional medicinal uses for treating joint pain, skin diseases, infections, and inflammation. The seed oil is applied for skin conditions, and powdered wood is used to treat leprosy and skin ailments. It also has antibacterial and anti-inflammatory properties and shows potential in managing diseases like Alzheimer's and certain cancers. Ecologically, its deep roots help prevent soil erosion, and its nitrogen-fixing ability improves soil fertility. Overall, Dalbergia sissoo is valued for its medicinal, agricultural, and environmental contributions.[13] Dalbergia sissoo (shisham) was listed in CITES Appendix II in 2016 due to concerns over illegal trade threatening rosewood species globally. Although abundant and fast-growing in South Asia, it remains listed because it is difficult to distinguish from other Dalbergia species in trade. Efforts to delist the species have not succeeded, but trade rules were eased to allow export of small items under 10 kg without permits, helping artisans. The listing aims to balance conservation needs with supporting sustainable trade and livelihoods.[14]
Turmeric:-
Turmeric has been used for almost 4,000 years, with its earliest usage documented in Vedic India, where it held significance as both a culinary spice and a substance used in religious rituals. By around 700 AD, turmeric had spread to China, reaching East Africa by 800 AD, West Africa by 1200 AD, and Jamaica in the 18th century. The famed traveler Marco Polo, in 1280, wrote with fascination about a spice resembling saffron. Sanskrit medical treatises—as well as the Ayurvedic and Unani systems—mention turmeric’s longstanding medicinal use across South Asia. For instance, Susruta’s Ayurvedic Compendium from 250 BC recommends a turmeric-based ointment to counteract food poisoning.[15]
Turmeric’s beginnings are believed to stretch back centuries, with many experts tracing its origins primarily to India, though some ancient texts and research suggest possible roots in other regions as well. This distinctive spice quickly became integrated into traditional Indian medicinal systems like Ayurveda and Siddha, celebrated for its wide-ranging healing effects. It was considered an effective remedy for a variety of health issues, such as digestive problems and joint discomfort. Ancient medicinal treatises praised turmeric’s anti-inflammatory and antioxidant benefits long before these qualities were scientifically validated by modern studies.[16]
Today, turmeric is widely cultivated in tropical regions around the world and is known by various names. In North India, it is called “haldi,” a term derived from the Sanskrit “haridra,” while in southern India it is called “manjal,” a name seen frequently in ancient Tamil texts. The English name “turmeric” comes from the Latin “terra merita” (“meritorious earth”), referring to the yellow hue of its ground form; other languages use similar nomenclature, such as terre merite? in French or simply “yellow root.” Many names for turmeric across cultures are derived from its Latin botanical name, curcuma. Notably, Sanskrit literature recognizes at least 53 different terms for turmeric, reflecting its cultural importance.[17]
India is the world’s leading producer, consumer, and exporter of turmeric, accounting for about 80% of global production and over 60% of exports. Indian turmeric is highly valued for its high curcumin content and is exported to countries like Bangladesh, UAE, USA, Malaysia, Morocco, and Iran. Major producing states include Maharashtra, Tamil Nadu, Telangana, Karnataka, Andhra Pradesh, Orissa, Assam, Kerala, and West Bengal. Turmeric is also grown in China, Myanmar, Nigeria, and Bangladesh, but India dominates global cultivation and trade. Indian turmeric is recognized for its quality and is used in food, medicine, cosmetics, and more, with proven anti-inflammatory, antioxidant, and other health benefits.[18]
In traditional Ayurvedic medicine, moringa is said to help treat as many as 300 different conditions. Moringa flower juice is believed to enhance lactation, while a tea made from its leaves is used to combat colds and infections. Fresh moringa leaves are traditionally used to treat anemia, gastric ulcers, and diarrhea. A paste made from the leaves is applied to insect bites, wounds, or fungal skin problems for its antibacterial and anti-inflammatory effects. Crushed moringa seeds are used to relieve cramps, rheumatism, arthritis, and as a natural antibiotic. Immature moringa seed pods, known as "drumsticks," are a popular ingredient in South Asian cuisine, often parboiled and cooked in curries. In the Philippines, moringa leaves are traditionally added to broth for soups. The plant is rich in essential nutrients, with its leaves and seeds containing 27 vitamins, 9 essential amino acids, 46 antioxidants, various minerals, and high protein levels, making it a powerhouse for health and well-being. Modern research confirms moringa’s traditional use as an anti-inflammatory and antioxidant agent. Studies show that moringa contains bioactive compounds such as quercetin and chlorogenic acid, which help reduce inflammation and oxidative stress, supporting its Ayurvedic use for treating inflammatory conditions and protecting against chronic diseases. [20,21]
MACHANISM OF ACTION :-
Shisham:-
The mechanism of action of the shisham plant (Dalbergia sissoo) involves several detailed anti-inflammatory processes. Shisham contains flavonoids and phenolic compounds that stabilize cell membranes, preventing the release of inflammatory mediators such as prostaglandins and cytokines by inhibiting enzymes like prostaglandin synthetase. Its extracts also reduce oxidative stress by scavenging free radicals and enhancing antioxidant enzyme activity.
Shisham’s anti-inflammatory effects are further demonstrated by its ability to inhibit protein denaturation, a process linked to inflammation and rheumatoid arthritis, through alteration of electrostatic, hydrogen, hydrophobic, and disulphide bonding. The plant’s extracts have shown dose-dependent inhibition of granuloma formation and reduction in pro-inflammatory cytokines, supporting its role in managing chronic inflammation. Additionally, shisham modulates immune responses and supports tissue repair, making it effective in treating inflammatory conditions and related tissue damage. [30,33]
Turmeric :-
Numerous in vitro and in vivo studies have demonstrated that curcumin, the active compound in turmeric, holds significant potential for treating various inflammatory diseases. Curcumin works by inhibiting key pro-inflammatory transcription factors such as NF-κB and AP-1,
Curcumin helps regulate immune cells and is beneficial for treating inflammatory diseases. It acts mainly on dendritic cells, T helper 17 (Th17) cells, and T regulatory (Treg) cells. Th17 cells promote inflammation by producing cytokines such as IL-17, IL-22, and IL-23, while Treg cells suppress inflammation. An imbalance between Th17 and Treg cells can lead to abnormal immune responses and inflammation. Curcumin inhibits differentiation of Th17 cells and helps restore balance between Treg and Th17 cells by blocking the IL-23/Th17 pathway.
Oxidative stress, caused by reactive oxygen species (ROS), worsens inflammation by activating inflammatory transcription factors. Curcumin reduces ROS by targeting NADPH oxidase and increasing antioxidant enzyme activity via the Nrf2-Keap1 pathway. This antioxidant action also contributes to curcumin’s anti-inflammatory effects.
In various inflammatory diseases such as inflammatory bowel disease, arthritis, psoriasis, depression, atherosclerosis, and COVID-19, curcumin reduces key inflammatory mediators by inhibiting transcription factors like NF-κB and AP-1, lowering cytokines (TNFα, IL-1β, IL-6, etc.), downregulating enzymes such as COX-2 and 5-lipoxygenase, and suppressing signaling pathways (MAPK, nitric oxide synthase). Curcumin’s modulation of these inflammatory and oxidative pathways underlies its wide-ranging therapeutic potential. [22,23]
Fig.No (4): [34]
Moringa:-
Chronic inflammation is closely linked to metabolic disorders such as non-alcoholic steatohepatitis (NASH) and glucose intolerance caused by a high-fat diet. Studies have shown that moringa (Moringa oleifera) can reduce the expression of key pro-inflammatory cytokines like IL-1β, IL-10, and IFN-γ in animal models, with quercetin and chlorogenic acid believed to play a major role in these effects. In obese mice, a diet containing fermented moringa extract significantly lowered pro-inflammatory cytokines in the liver, adipose tissue, and muscle. Moringa not only inhibits the expression of pro-inflammatory factors but also helps regulate immune cells, making it a promising option for managing chronic inflammation.In laboratory studies, moringa leaf extract was found to inhibit COX-2 and reduce levels of pro-inflammatory cytokines (IL-1β, IL-6, PGE2, TNF-α) in immune cells. Using advanced techniques, researchers identified 15 phytochemicals in moringa that bind to COX-2, with quercetin and kaempferol flavonoid glycosides—especially those with acetylated glycosyl side chains—showing strong antioxidant and anti-inflammatory activity. Molecular docking confirmed these compounds bind competitively to COX-2, supporting moringa’s potential as a natural remedy for inflammation and its use in functional foods or healthcare products [24,25]
Dalbergin, an isoflavonoid found in Dalbergia sissoo, is known for its anti-inflammatory and antioxidant properties. Orientin, a flavonoid glycoside, helps neutralize free radicals and may support skin repair. Luteolin, commonly present in the heartwood, aids in modulating the release of cytokines. β-sitosterol, a plant sterol, has been linked to improved lipid profiles in animal studies.In Ayurvedic medicine, the tikta (bitter) and kashaya (astringent) rasa properties of shisham are considered key to its ability to pacify Vata and Pitta doshas, supporting deep tissue healing. Experimental studies in rats have shown that shisham extract can suppress COX-2 enzyme activity by up to 45% at certain concentrations. In vitro research suggests orientin may influence collagen synthesis, providing a plausible mechanism for wound healing. While human clinical trials are limited, the available data supports traditional claims regarding shisham’s anti-inflammatory and healing effects.[12]
Fig.No.:- (5).[32]
Mechanism of Action of Turmeric, Moringa, Shisham in Combination:-
The combination of turmeric, moringa, and shisham (Dalbergia sissoo) in Anti-inflammatory formulations produces a synergistic effect, targeting multiple pathways involved in inflammation. Turmeric’s active compound, curcumin, inhibits key pro-inflammatory transcription factors such as NF-κB and AP-1, reduces the production of cytokines like TNFα, IL-1β, IL-6, and IL-8, and down-regulates. enzymes including COX-2 and 5-lipoxygenase. Curcumin also activates antioxidant pathways like Nrf2, which helps combat oxidative stress.
Moringa contributes additional anti-inflammatory and antioxidant effects through compounds such as quercetin and chlorogenic acid, which further suppress NF-κB and other inflammatory mediators. Shisham’s flavonoids and phenolic compounds inhibit pro-inflammatory enzymes and cytokines, complementing the actions of turmeric and moringa.
When these agents are combined, they enhance each other’s bioavailability and efficacy, resulting in a broader and more potent anti-inflammatory effect. This synergy allows for lower doses of each component, reducing the risk of side effects while maximizing therapeutic outcomes. The multi-target approach is particularly effective in managing chronic inflammatory conditions and diseases associated with oxidative stress.[26,27]
Chronic inflammation is a root cause of many health problems, including arthritis, diabetes, heart disease, and digestive disorders. Combining moringa and turmeric helps address this underlying inflammation effectively. Turmeric works by inhibiting inflammatory enzymes like COX-2, lowering levels of CRP (C-reactive protein), and soothing inflamed tissues. Moringa acts at the cellular level to slow inflammation and contains compounds such as isothiocyanates that help prevent tissue damage. This combination is especially powerful for managing conditions like joint pain or arthritis, digestive inflammation (such as IBS or leaky gut), skin issues like eczema or acne, post-workout recovery, and general immune support. The synergistic effects of moringa and turmeric provide broad anti-inflammatory and antioxidant benefits, making them a valuable natural approach for supporting overall health and well-being. [26,29]
Shisham (Dalbergia sissoo) and moringa work together to combat inflammation through complementary mechanisms. Shisham contains flavonoids and phenolic compounds that stabilize cell membranes, inhibit the release of inflammatory mediators, and suppress pro-inflammatory enzymes and cytokines such as TNF-α and IL-6.[30] Moringa contributes anti-inflammatory and antioxidant effects via compounds like quercetin, chlorogenic acid, and isothiocyanates, which further suppress NF-κB and inflammatory mediators, and help reduce oxidative stress. [31] Together, these plants enhance each other’s bioavailability and efficacy, resulting in a broader and more potent anti-inflammatory effect, making them effective for managing chronic inflammatory conditions and oxidative stress-related diseases.[32]
Physicochemical properties of the turmeric and moringa relevant to inflammation management.
Fig.No:(6)[42]
Turmeric: Key Physicochemical Properties:-
Fig.No:(7)[46]
Fig No:(8) [43]
Moringa: Physicochemical Properties Relevant to Inflammation :-
Fig.No:(9) [50]
Pharmacological Activities :-
Shisam:-
Anti-inflamatory & Analgesic Activity of the Drug:-
Hexane and methanol extracts of Dalbergia sissoo leaves, along with the compound okanin, were assessed for anti-inflammatory activity using carrageenan-induced paw edema in rats, with the methanolic extract showing the greatest effect. A 90% ethanolic bark extract also demonstrated dose-dependent inhibition of paw edema in Wistar rats, with the 1000 mg/kg dose exhibiting the strongest anti-inflammatory activity over 120 minutes.
The methanolic leaf extract reduced pain behaviors in mice using acetic acid-induced writhing and hot plate tests, showing both peripheral and central analgesic effects. It achieved 68.2% inhibition of paw edema at 600 mg/kg, comparable to 73.4% inhibition by the standard drug diclofenac (5 mg/kg).
Alcoholic seed extracts exhibited peripheral analgesic effects in acetic acid writhing and Randall-Selitto tests, and central analgesic activity was confirmed in the hot plate, but not tail-clip, test in mice. These extracts also showed significant antipyretic effects in Brewer’s yeast-induced fever models.[50,51]
Ethanol extracts of bark displayed dose-dependent central analgesic effects in the tail-flick test in rats, with significant increases in pain latency at doses of 300-1000 mg/kg comparable to aspirin. Leaf ethanol extracts showed both peripheral and central analgesic activities in several tests, with antipyretic effects comparable to aspirin at higher doses and lasting up to 6 hours.
In summary, Dalbergia sissoo extracts from bark, leaves, and seeds exhibit strong and dose-dependent anti-inflammatory, analgesic (both central and peripheral), and antipyretic activities across a range of established animal models, often comparable to standard drugs like diclofenac and aspirin. These activities reinforce the potential of Dalbergia sissoo as a natural therapeutic agent for managing inflammation and pain. [50, 51]
Anti-Diabetic activity :-
Research with leaf extracts at 300 mg/kg, prepared with solvents like ethyl acetate, ethanol, n-butanol, and petroleum ether, found that the ethanolic extract provided stronger blood sugar-lowering effects than the standard drug glibenclamide (Sangram et al., 2009). Studies with ethanolic bark extracts at 250–500 mg/kg doses in diabetic rats also showed significant reductions in blood glucose (Shukla et al., 2000). Blood analyses revealed that treatment lowered triglycerides, total cholesterol, LDL, and VLDL, while increasing HDL levels; the effects were again compared to glibenclamide as a standard reference (Sayanti et al., 2014; Kiran V et al., 2012). [52, 53]
Both alcoholic and aqueous bark extracts produced pronounced anti-diabetic effects in type 2 diabetic rats induced by streptozotocin and nicotinamide, with marked reductions in blood glucose levels. These extracts were also rich in polyphenols and chlorogenic acid, which are considered responsible for their hypoglycemic action (Shivani Saini & Sunil Sharma, 2013). Animal studies further demonstrate improvement in antioxidant status (elevated GSH, SOD, CAT; reduced MDA) and restoration of healthy lipid profiles, along with increased body weight in diabetic models. [54,52]
In summary, Dalbergia sissoo extracts—particularly ethanolic forms from leaves and bark—effectively lower blood sugar and improve lipid balance, with key mechanisms attributed to their polyphenol and chlorogenic acid content, and often perform as well as or better than standard antidiabetic medications in research settings.[52,53,54]
Antibacterial & Antiprotozoal activities:-
Antiprotozoal:-
Dalbergia sissoo has been investigated for its antiprotozoal effects against Lamblia trophozoites. In the study by Naveeda et al. (2012), different dilutions of aqueous extracts from Dalbergia sissoo heartwood were used. The heartwood contains phytochemicals such as lignin, benzene-ethanol soluble compounds, and alpha cellulose. The viability of the trophozoites was assessed using a hemocytometer and trypan blue dye to count live cells. This method enabled the evaluation of the aqueous extract’s effectiveness in reducing the number of viable protozoan cells.
In summary, the research shows that aqueous extracts of Dalbergia sissoo heartwood contain bioactive compounds that exhibit antiprotozoal activity by decreasing viable Lamblia trophozoites in a dose-dependent manner. [55]
Antibacterial:-
Dalbergia sissoo has been extensively studied for its antibacterial properties against various pathogenic bacteria including Micrococcus luteus, Escherichia coli, Staphylococcus aureus, Raoultella planticola, and Acinetobacter species. Research on the leaf and bark extracts using solvents such as chloroform, ethyl acetate, acetone, and methanol at a concentration of 100 mg/ml demonstrated effective antibacterial activity. Specifically, the methanolic extract exhibited the highest efficacy against Staphylococcus aureus. Moreover, studies investigating bacterial resistance to the hexane extract reported that Dalbergia sissoo showed superior antibacterial potential compared to some commercial antibiotics, indicating its promising role as a natural antimicrobial agent. [55,56]
Ostiogenic Activity :-
Dalbergiphenol (DGP), a neoflavonoid extracted from Dalbergia sissoo heartwood, was tested for its effects on bone loss using ovariectomized adult BALB/c mice. Over six weeks, mice received oral DGP (1 or 5 mg/kg/day) or 17β-estradiol (E2), with sham and vehicle-treated ovariectomized mice as controls. While OVX mice showed weight gain and bone loss, DGP-treated mice maintained bone volume and strength similar to E2-treated controls but without the uterine estrogenic effects seen with E2. DGP increased bone formation and osteoblast-associated gene expression (Runx2, osterix, collagen type I) while decreasing osteoclast activity markers, indicating it promotes bone formation and reduces resorption. [57,58]
Additionally, a butanol-soluble extract from Dalbergia sissoo leaves and pods (BSSF) improved bone microarchitecture and strength in ovariectomized rats, reduced bone turnover markers, inhibited osteoclastogenic gene expression, and enhanced osteogenic gene expression, effects comparable to 17β-estradiol.
Five isoflavonoid compounds from leaves, including a new glucoside caviunin 7-O-[β-D-apiofuranosyl-(1→6)-β-D-glucopyranoside] (CAFG), and known compounds genistein, biochanin A, and pratensein, demonstrated osteogenic potential in primary osteoblast cultures, increasing alkaline phosphatase activity and mineralization. CAFG showed the strongest effects and acted independently of estrogen receptor signaling. CAFG also stimulated bone formation in ovariectomized mice by enhancing BMP2 and Wnt/β-catenin signaling pathways, promoting osteoblast proliferation, survival, and differentiation, increasing osteoprotegerin expression, and inhibiting osteoclast activation. It improved bone biomechanical properties and reduced bone turnover more effectively than genistein, without causing uterine hyperplasia. CAFG also accelerated cartilage formation and bone repair post-injury. Overall, Dalbergia sissoo compounds and extracts demonstrate robust osteogenic and antiresorptive effects, making them promising candidates for treating osteoporosis and enhancing bone repair.[59]
Dermatological Actvity:-
The cytotoxicity and in vitro melanogenic effects of Dalbergia sissoo bark were assessed using the MTT assay on melanoma cells, showing that the ethyl acetate extract was non-toxic and significantly enhanced melanin production compared to hexane and ethanol extracts (Prof. Dr. Ali Esmail, 2017). Additionally, methanolic extracts of leaves, fruits, and bark were analyzed for their photoprotective and DNA-protective properties in vitro, alongside an investigation into their phytochemical composition, highlighting their potential dermatological benefits (Shagufta Yasmeen and Promila Gupta, 2016). Together, these studies suggest that Dalbergia sissoo extracts possess promising skin-protective and pigmentation-enhancing activities, supporting their therapeutic potential for dermatological applications. [55,59]
Other Pharmacological Activities:-
Gastroprotective Action:-
Dalbergia sissoo stem bark methanol extract (DSME) has demonstrated significant gastroprotective effects in rats with diclofenac sodium-induced ulcers. The protective action is likely due to its antioxidant and cytoprotective properties. DSME administration decreased ulcer severity, lipid peroxidation, and inflammatory markers in gastric tissues while simultaneously enhancing the activity of antioxidant enzymes and increasing gastric mucosal defense by boosting mucus content and balancing gastric acid secretion, including lowering acidity and increasing pH. Histological studies further confirmed these protective effects, showing reduced tissue damage. These results suggest that DSME can effectively mitigate gastric ulcer formation by scavenging free radicals, restoring enzymatic antioxidants, and providing cytoprotection against nonsteroidal anti-inflammatory drug (NSAID)-induced gastric irritation.[51]
Neuroprotective Action:-
In neuroprotection studies, the ethanolic extract of Dalbergia sissoo leaves was given orally to rats with neurotoxicity induced by 3-nitropropionic acid at doses of 300 and 600 mg/kg. The extract improved cognitive functions, memory, and learning in mice as observed in behavioral paradigms and ameliorated oxidative stress by enhancing antioxidant defenses and reducing acetylcholinesterase activity in brain tissue. It reversed cerebral ischemia-induced damage by normalizing brain weight and antioxidant levels, and histopathological examinations showed protection of brain tissues. The extract attenuated behavioral and biochemical alterations associated with neurotoxicity, highlighting its potential to manage neurological disorders through antioxidant, anti-inflammatory, and estrogen-like mechanisms.[51]
Reproductive Action:-
The ethanol extract of Dalbergia sissoo stem bark shows strong anti-spermatogenic effects both in vitro and in vivo. In studies with semen from healthy men, the extract caused a dose- and time-dependent reduction in sperm motility and viability, with complete immobilization at 20 mg/mL within 3 minutes. In mice, oral administration of 200 mg/kg significantly reduced testis and epididymis weight, sperm motility, and sperm count. Histological examination revealed degenerative changes in reproductive tissues. Similarly, aqueous leaf extracts given to male mice decreased sperm motility, viability, and count, along with lower testosterone levels, but these effects were reversible after stopping treatment, indicating potential as a male contraceptive without toxicity or libido effects.[59]
Antioxidant Activity:
Leaf extracts have potent antioxidant effects, reportedly nearly twice as powerful as common antioxidants like vitamin E and selenium. This contributes to the protective effects observed in various oxidative stress-related conditions. [51,59]
Additional pharmacological activities include antipyretic (fever-reducing), anticoagulant, antidiarrheal, immunomodulatory, reproductive, and anti-spermatogenic properties.
Turmeric(Curcuma Longa):-
Anti- Inflammatory :-
Curcumin, the principal compound in turmeric, exerts its anti-inflammatory effects by modulating several critical signaling pathways. It inhibits the nuclear factor-kappa B (NF-κB) pathway by preventing degradation of its inhibitor (IκBα) and reducing phosphorylation of NF-κB subunits, which leads to decreased activation of inflammatory genes. Curcumin also blocks the mitogen-activated protein kinase (MAPK) pathway by inhibiting phosphorylation of key kinases such as ERK, JNK, and p38, reducing expression of pro-inflammatory cytokines like tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and interleukin-8 (IL-8). Additionally, curcumin downregulates the JAK-STAT pathway and inhibits activation of inflammasomes such as NLRP3, thereby reducing chronic inflammation. This multifaceted suppression of inflammatory mediators and signaling cascades helps alleviate various inflammatory conditions and contributes to curcumin’s therapeutic potential. [60,61]
Antioxidant Activity:-
Curcumin’s antioxidant effects are largely linked to its unique chemical structure, which includes carbon-carbon double bonds, β-diketo groups, and phenyl rings substituted with hydroxyl and o-methoxy groups. These structural features enable curcumin to act as a free radical scavenger and hydrogen and electron donor, neutralizing reactive oxygen species (ROS) such as superoxide radicals, hydrogen peroxide, and nitric oxide. Studies using laser flash photolysis and pulse radiolysis have clarified these mechanisms.
Curcumin enhances the activity of various antioxidant enzymes like superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and heme oxygenase-1 (OH-1). It also boosts glutathione levels by upregulating glutathione transferase and related mRNAs. Additionally, curcumin inhibits enzymes that generate ROS, including lipoxygenase (LOX), cyclooxygenase (COX), and xanthine oxidase, and chelates metal ions that catalyze oxidative reactions. Due to its lipophilic nature, curcumin functions as a chain-breaking antioxidant by scavenging peroxyl radicals and preventing lipid peroxidation, thereby protecting cell membranes from oxidative damage.
Furthermore, curcumin regulates antioxidant gene expression through signaling pathways like Keap1-Nrf2/ARE, helping maintain redox balance in cells. These combined chemical and biological actions contribute to curcumin’s potent antioxidant capacity effective against oxidative stress-related diseases. [62,63,64]
Anticancer Activity :-
Curcumin, the primary active compound in turmeric, exhibits anticancer effects through multiple intricate mechanisms involving the modulation of various cellular signaling pathways. It inhibits cancer cell proliferation and tumor growth by targeting pathways such as PI3K/Akt/mTOR, MAPK, Wnt/β-catenin, NF-κB, Hedgehog, Notch, and JAK/STAT3. By suppressing these pathways, curcumin effectively hampers the signaling vital for tumor survival and progression [65,66,67]
One key anticancer mechanism of curcumin is the induction of apoptosis. Curcumin upregulates pro-apoptotic proteins including Bax and caspases, while downregulating anti-apoptotic proteins such as Bcl-2 and Bcl-xL, promoting the programmed death of cancer cells. This enhances the removal of malignant cells. Moreover, curcumin causes cell cycle arrest by modulating cyclins and cyclin-dependent kinases, thereby preventing uncontrolled cell division. [68]
Curcumin also inhibits tumor invasion, metastasis, and angiogenesis, which are critical for cancer spreading. It downregulates vascular endothelial growth factor (VEGF), a key molecule promoting new blood vessel formation in tumors, and suppresses genes involved in metastasis, reducing cancer dissemination.[69]
Curcumin has also been shown to enhance the effectiveness of chemotherapy and radiotherapy by sensitizing cancer cells, overcoming drug resistance mechanisms, and improving treatment outcomes without significant toxicity. [65,68]
Anti-Microbial Activity:-
Turmeric’s active compound, curcumin, demonstrates strong antimicrobial activity against a wide range of bacteria, fungi, and viruses. It disrupts bacterial cell membranes, interferes with DNA replication, and modulates genes critical for microbial survival. Curcumin is effective against both Gram-positive bacteria like Staphylococcus aureus and Gram-negative bacteria such as Escherichia coli and Klebsiella pneumoniae. It inhibits biofilm formation and enhances antibiotic effectiveness by overcoming resistance. Curcumin also disrupts fungal membranes and metabolic processes and hinders viral replication and entry. In vivo, curcumin can eradicate Helicobacter pylori and reduce tissue damage from infections. These effects highlight turmeric’s potential as an alternative or complementary antimicrobial therapy. [70,71,72]
Anti-Lipidemic & Hypoglycaemic Activity:-
Preclinical and clinical studies show that turmeric extract or curcumin supplementation in hyperlipidemia animal models significantly reduces plasma total cholesterol, free fatty acids, and especially triglycerides, often returning them near normal levels. Curcumin also improves symptoms of excessive alcohol consumption and non-alcoholic fatty liver disease. In type 2 diabetes mellitus (T2DM), which accounts for about 90% of diabetes cases and is characterized by insulin resistance and pancreatic dysfunction, curcumin significantly lowers glycated hemoglobin (HbA1c) and fasting blood glucose levels. It also improves metabolic syndrome parameters by reducing LDL cholesterol, triglycerides, fasting blood sugar, insulin resistance (HOMA-IR), aminotransferase (AST) levels, and body weight. Curcumin inhibits carbohydrate-digesting enzymes and glucose transporters in the intestine, thereby suppressing glucose absorption and reducing blood sugar spikes after meals. Recent computational studies suggest curcuminoids bind multiple diabetes-related molecular targets, supporting their potential for anti-diabetic effects. Curcumin can be used alone or alongside other anti-diabetic and lipid-lowering drugs, though more clinical trials are needed for confirmation. [73]
Cardioprotective Activity:-
Clinical research shows that curcumin has antihypertensive effects by lowering blood pressure and improving heart blood flow. It reduces blood viscosity and prevents blood clot formation by inhibiting thromboxane A2 synthesis and regulating calcium signals to stop platelet activation and aggregation. Curcumin may increase menstrual bleeding due to its effect on platelet aggregation, so its use during menstruation should be cautious. Additionally, curcumin protects vascular endothelial cells by inhibiting NF-κB, AKT, and ERK pathways, helping prevent arterial sclerosis, thrombosis, and abnormal blood pressure. Clinical studies also found that curcumin reduces the recurrence of coronary artery obstruction and prevents complications in patients with vascular stents in coronary arteries.[74]
Immunomodulating Activity :-
Curcumin enhances immune function by activating immune cells while reducing excessive inflammation and allergies. It suppresses key inflammatory pathways such as NF-κB, MAPKs, JAK/STAT, β-catenin, and Notch-1, thereby regulating pro-inflammatory cytokines like IL-1β, TNF-α, IL-2, IL-6, and IL-10. Clinically, curcumin has therapeutic potential in autoimmune diseases including lupus, rheumatoid arthritis, ankylosing spondylitis, and psoriasis. It helps restore T cell function, boosting the body's ability to fight cancer cells and pathogens. Both lab and animal studies confirm that curcumin inhibits cancer cell proliferation and induces apoptosis.[74]
Other Activities like antiviral, neuroprotective, hepatoprotective, properties, often mediated through its anti-inflammatory and antioxidant mechanisms, as well as modulation of various signaling pathways
Moringa:-
Anti-inflamatory Activity:-
Moringa shows a variety of pharmacological effects such as antioxidant, anti-inflammatory, hepatoprotective, and antidiabetic activities. It helps lower blood glucose and cholesterol, protects the liver, supports heart and brain health, relieves pain, modulates the immune system, and fights microbes. Clinical evidence supports its benefits in improving metabolic health, anemia, and inflammatory conditions. These properties make moringa a promising natural remedy for multiple chronic diseases.[75]
Anti-Diabetic Activity:-
Aqueous extract of Moringa oleifera leaves demonstrates anti-diabetic effects by helping control diabetes and maintaining blood sugar levels. Studies on methanol extracts of Moringa oleifera pods in streptozotocin (STZ)-induced diabetic rats showed that treatment with the extract at doses of 150 or 300 mg/kg over 21 days significantly lowered serum glucose and nitric oxide levels, while increasing insulin and protein levels. Additionally, the antidiabetic effect of Moringa seed powder was investigated at doses of 50 and 100 mg/kg in STZ-induced diabetic male rats, where untreated diabetic rats exhibited elevated levels of IL-6 and lipid peroxides, coupled with decreased antioxidant enzymes in serum and kidney tissues. [75,76]
Wound Healing activity:-
Studies demonstrate that Moringa oleifera leaf extracts, particularly ethyl acetate and aqueous preparations at 300 mg/kg, significantly enhance wound healing by promoting wound closure, increasing the strength of granulomas, and reducing skin rupture in scar areas. In diabetic models, leaf extracts help downregulate inflammatory markers and boost vascular endothelial growth factor levels in damaged tissues. Aqueous extracts showed superior cell proliferation and migration, aiding tissue regeneration in wound healing assays.[77]
Antifertility & Fertility Activity:-
The various parts of Moringa oleifera exhibit notable effects on fertility and abortion. Studies have found that aqueous extracts at doses of 200 and 400 mg/kg show pronounced abortifacient and anti-fertility properties. Recent research on both hot and cold leaf extracts suggests that consuming Moringa before, during, or after pregnancy may cause strong uterine contractions, potentially leading to adverse effects on fetal development. [77,78]
Anticancer Activity:-
Moringa oleifera displays significant anticancer activity, especially through extracts from its leaves and bark. Studies show that these extracts reduce cell survival and proliferation, induce apoptosis, and block colony formation in breast (MDA-MB-231) and colorectal (HCT-8) cancer cell lines. Key bioactive compounds, including eugenol and isothiocyanates, contribute to these effects by targeting cancer-related proteins and pathways. Moringa root extracts also demonstrate selective cytotoxicity against various cancer cells while sparing normal cells. Additionally, methanolic leaf extracts have shown potent anti-prostate cancer effects by inhibiting the Notch signaling pathway and inducing apoptosis via regulation of Bax and Bcl-2 expression. Overall, moringa’s anticancer effects span multiple cancer types and involve inhibiting cell growth, inducing cell death, and modulating critical oncogenic pathways.[79,80,81]
Other Pharmacological Activities:-
Industrial & Commercial:-
Pharmaceutical and Nutraceutical Use
Functional Food & Beverages:-
Cosmetics & Personal Care Product:-
Traditional and Herbal Medicine:-
Commercial Crop Cultivation :-
Toxicological Study Of The Combination Of Shisham, Turmeric, Moringa Plant:-
FUTURE PROSPECTIVES :-
RESULT:
The result is based on the individual studies and review findings of Shisham, Turmeric, and Moringa, each showing significant anti-inflammatory potential. Each plant contributes unique bioactive compounds: Shisham offers flavonoids, tannins, and glycosides; Turmeric is rich in curcumin, which inhibits COX-2, TNF-α, and NF-κB; and Moringa contains flavonoids, phenolic acids, glucosinolates, and isothiocyanates, all known for their anti-inflammatory and antioxidant effects. Based on their proven bioactive compounds and mechanisms, these plants may provide a synergistic anti-inflammatory effect when combined, enhancing therapeutic activity compared to using them alone.
DISCUSSION:
The review of the anti-inflammatory activity of Shisam, turmeric, and moringa highlights the therapeutic potential of these traditionally used medicinal plants. Turmeric, rich in curcumin, has been extensively studied and consistently demonstrates strong anti-inflammatory effects through inhibition of COX-2, TNF-α, IL-6, and NF-κB pathways. Moringa oleifera also shows significant activity due to bioactive compounds such as quercetin, kaempferol, and isothiocyanates, which help reduce oxidative stress and inflammatory mediator release. Shisam, though comparatively less studied, contains flavonoids and phenolic compounds that contribute to moderate but meaningful anti-inflammatory effects, especially in models of edema and chronic inflammation. Collectively, the evidence suggests that these plants possess complementary mechanisms—antioxidant action, suppression of pro-inflammatory cytokines, and modulation of signaling pathways—making them promising candidates for developing safer, plant-based anti-inflammatory formulations. However, further standardized clinical studies are needed to confirm their efficacy, safety, and synergistic potential.
CONCLUSION:-
This review demonstrates that Dalbergia sissoo, Curcuma longa, and Moringa oleifera possess extensive pharmacological capabilities that hold significant potential for modern therapeutic use. Across numerous studies, these plants show strong anti-inflammatory, antioxidant, antidiabetic, antimicrobial, osteogenic, and anticancer effects, largely driven by their rich content of flavonoids, polyphenols, curcuminoids, and isothiocyanates. Their ability to interact with multiple biochemical pathways provides scientific support for their traditional medicinal applications. Despite these encouraging findings, much of the evidence remains preclinical. Advancing the medicinal use of these botanicals will require standardized extract formulations, clearer dosing guidelines, and comprehensive human trials. Nonetheless, the alignment of traditional knowledge with growing scientific evidence suggests that these plants are valuable candidates for developing safe, natural, and versatile therapeutics—particularly within the rising global interest in herbal and integrative medicine.
REFERENCES
Prajakta Vidhate, Godavary Brahma, Mugdha Joshi, Aryan Satpute, Shalaka Katkar, Apurva Kamble, Vedika Andhale, Review on Study of Anti-Inflammatory Activity using Moringa, Shisham, and Turmeric, Int. J. of Pharm. Sci., 2025, Vol 3, Issue 12, 2479-2507. https://doi.org/10.5281/zenodo.17942377
10.5281/zenodo.17942377