View Article

Abstract

Stomach or duodenal ulcers are signs of peptic ulcer disease (PUD), a common gastrointestinal condition. The primary causes of PUD are Helicobacter pylori infection and the use of nonsteroidal anti-inflammatory medications (NSAIDs). If therapy is not performed, it may result in intestinal issues such as bleeding, perforation, and obstruction. The symptoms of PUD include nausea, vomiting, heartburn, regurgitation, and stomach pain. There are various synthetic medications available to treat ulcers. However, these medications are more expensive than herbal remedies and are more likely to cause adverse side effects. The use of herbal medicine is crucial, and limits are necessary to ensure the quality of the product. Specifically, randomised studies were conducted to determine their efficacy and safety in treating ulcers. However, these medications are more expensive than herbal remedies and are more likely to cause adverse side effects. The use of herbal medicine is crucial, and limits are necessary to ensure the quality of the product. Specifically, randomised studies to determine their efficacy and safety in treating ulcers. This review examines the current scientific understanding of P. Alba's botanical description, phytochemistry, pharmacological qualities, and potential applications. According to one study, the plant has different bioactive chemicals with potential medical applications, including antibacterial, anti-arthritic, and antioxidant characteristics.

Keywords

Peptic ulcer disease (PUD), Gastric ulcer, Duodenal ulcer, Helicobacter pylori, Nonsteroidal anti-inflammatory drugs (NSAIDs), Herbal medicine, Medicinal plants, Plumeria alba, Anti-ulcer Activity.

Introduction

A rupture in the normal integrity of the gastric mucosa that extends through the muscularis mucosa into the sub mucosa or deeper is known as a gastric ulcer, also known as a stomach ulcer. An imbalance between the mucosal defensive forces (mucus bicarbonate, blood flow, and prostaglandins) and the stomach aggressive factors (acid, pepsin, H. pylori, and non- steroidal anti-inflammatory drugs) leads to peptic ulcers. [1] Although there are several causes of peptic ulcer disease (PUD), Helicobacter pylori-associated PUD and NSAID associated PUD make up the majority of the illness's pathogenesis [2].

Types of Ulcer

  1. Duodenal Ulcer
  2. Gastric Ulcer
  3. Esophageal Ulcer

Duodenal ulcer

Peptic ulcer disease is a broad spectrum of illnesses that includes duodenal ulcers. The state of illness and clinical "Peptic ulcer disease" refers to symptoms that arise from a disturbance in the mucosal membrane of the stomach or duodenum, the first segment of the small intestine. Pre-epithelial, epithelium, and subepithelial components make up the anatomical protection system on the surfaces of the stomach and duodenum. Damage to the mucosal surface underneath the superficial layer results in ulceration. [3]

Gastric Ulcer

Gastric ulcer disease is more commonly known as peptic ulcer disease (PUD), which refers to ulcers that can occur in the stomach and the proximal duodenum (the two organs most frequently impacted by the secretion of pepsin and gastric acid), though the lower esophagus, distal duodenum, and jejunum can also be affected, albeit to a lesser extent [4].

Esophageal ulcer

An esophageal ulcer is an obvious break in the mucosal membrane of the esophagus. injuries brought on by esophageal reflux. According to endoscopic examination, the majority of patients have some degree of hiatal hernia, and gastroesophageal reflux syndrome is the most common cause of esophageal ulcers. [5]

However, there was individual variation in the pathogenicity of HP, which was impacted by both environmental and genetic variables. Ironically, HP-induced chronic gastritis seems to protect against gastroesophageal reflux disease (GERD), making its role in stomach health and disease more difficult to grasp [6] Individual susceptibility is demonstrated by the fact that peptic ulcers only occur in a small percentage of infected or NSAID-using people. Interleukin 1β (IL1B) and other cytokine genes have genetic variations. According to observations, these issues are NSAID users were four times more likely, while aspirin users were twice as probable. The risk of upper gastrointestinal bleeding increases when anticoagulants, corticosteroids, and selective serotonin reuptake inhibitors (SSRIs) are used concurrently. NSAIDs, aspirin, and H. pylori infection appear to have separate hazards, according to a meta-analysis. About one-fifth of cases are idiopathic peptic ulcers, which are H. pylori-negative, NSAID-negative, and aspirin-negative [7-10]. Peptic ulcer disease's age- standardised prevalence rate dropped from 143·4 per 100,000 population in 1990 to 99·4 per 100,000 people in 2019, which coincided with declines in disability-adjusted life years and mortality.[11] Peptic ulcers are treated with a variety of drug classes, such as antimicrobials (metronidazole and clarithromycin), inhibitors of proton pumps that block the H+, K+ ATPase pump (omeprazole and lansoprazole), blocking agents of the H2-receptor (cimetidine and ranitidine), and drugs that disrupt the bacterial cell wall (bismuth salt). The majority of these medications have serious drug-drug interactions that limit their potential usage, as well as unfavourable side effects include gynecomastia, hypersensitivity, impotence, arrhythmia hematopoietic alterations, and renal illness [12]. In many regions of the world, plants have offered beneficial sources of nutrients and medicinal preparations for the treatment of various medical ailments. When compared to manufactured pharmaceuticals, the great majority of people who use plant extracts as medicine believe they are safer. [13] Numerous preclinical investigations have revealed the anti-ulcerative activities of a number of chemical compounds obtained from plants. These components are classified as alkaloids, tannins, terpenoids, flavonoids, glycosides, carotenoids Numerous Alkaloids, tannins, flavonoids, terpenoids, glycosides, carotenoids, and saponins are among the ingredients.[14-16]

Plumeria alba

Traditional medicine has been based on plants for generations, using their bioactive compounds to cure a variety of illnesses. Plumeria alba, often known as white frangipani, is widely used for its therapeutic properties in a number of regions. It is often found in gardens and temples and serves both decorative and medicinal purposes. Contemporary phytochemical and pharmacological studies have begun to support conventional claims and investigate their application in contemporary medicine [17]. It is a member of the Apocynaceae family. The bark, leaves, and flowers of P. alba have been found to contain a variety of bioactive components with strong antibacterial, anti-inflammatory, anthelmintic, antipyretic, and antirheumatic qualities. Skin conditions like herpes, scabies, and ulcers are treated using the stem and leaf of P. alba. [18-20] White Champa, also known as Plumeria alba Linn (Apocynaceae), is a tiny lactiferous tree or shrub that is indigenous to tropical America. Occasionally grown in the gardens, it stands 4.5 meters tall. The plant is mostly cultivated for its fragrant and decorative blossoms. Lanceolate leaves are present. The plant produces white flowers with golden centers. In corymbose fascicles, fragrant Frangipani is renowned for its spiral-shaped blossoms and strong scent [21] A combination of amyrins, ß- sitosterol, scopotetin, the iriddoids isoplumericin, plumieride, plumieride coumerate, and plumieride coumerate glucoside are believed to be present in the plant. [22-23]

 

 

Fig:1 Plumeria alba

The floral oil is mostly composed of primary alcohols such as geraniol, citronellol, farnesol, and phenyl ethyl alcohol, with a trace quantity of linalool. The flowers include kaempferol and quercetin. [24]

Taxonomical classification [25]

Kingdom

Plantae

Super division

Spermatophyta

Division

Magnolliophyta

Class

Magnoliopsida

Sub class

Aateridae

Order

Gentianales

Family

Apocynaceae

Genus

Plumeria

Phytochemical constituents

Chemicals like amyrin, scopotein, iridoid isoplumericin, plumerein, plumeride cumarate, and plumeride cumarate glycoside are found in white frangipani. Plumierin, resinic acid, fulvoplumierin, terpeneoid combination, sterol, and plumeride are found in the leaves and bark. Additionally, cytotoxic iridoid, allamcin, allamandin, 2, 5-dimethoxy-p-benzoquinone, plumericin, and liriodindrin are found in the bark. Alkaloid, tannin, and iridoid are also present in white frangipani roots [26]

Steroids, flavonoids, and alkaloids were found in the P. alba flower extract during preliminary phytochemical screening. Eicosanoid production can be disrupted by flavonoids. By preventing neutrophils from degranulating, flavonoids can also lower the synthesis of arachidonic acid. Alkaloids have also been linked to the capacity to reduce pain perception in addition to flavonoids. The plant may include phytoconstituents that act on central opioid receptors or inhibit the cyclooxygenase enzyme. [27] The biological actions of P. alba essential oils have been the subject of further research. Liu et al. investigated the antibacterial, antioxidant, and antipyretic-analgesic properties of P. alba flower essential oil and suggested that the bioactivity may be attributed to the essential oil's primary constituents, including benzyl salicylate, benzyl benzoate, germacrene B, and linalool. [28]

Terpenoids, tannins, diterpenes, triterpenes, flavonoids, flavonols, coumarins, steroids, saponins,  alkaloids, quinones,  and  phenols  are  examples  of  phytoconstituents. and glycosides typically have important roles in antifungal, antibacterial, antibiotic, and antinutritional activities [29]

Pharmacological Effects

Anti-microbial

The leaf and flower extracts exhibit a variety of antibacterial qualities against fungus like Candida albicans and bacteria like E. coli and Staphylococcus aureus. [30]

When it comes to the uro-gastro pathogenic Escherichia coli, one of the prevalent bacteria with pathogenic strains that are comparatively resistant to synthetic medications, P. alba seems to have a considerable antibacterial ability that resembles a broad range antibiotic. This fragrant plant may be a source of newly developed antibacterial compounds as well as a non-toxic agent that produces antibiotics. Particularly against E. coli, frangipani extracts have the potential to be a natural source of anti-toxic antibiotics. [31]

Antipyretic and Analgesic Properties

Plumeria extracts have been demonstrated to have antipyretic (fever-reducing) and analgesic (pain-relieving) qualities, suggesting that they may be utilized as natural remedies for fever and pain. [32]

Anti-oxidant

Numerous pathologic conditions, including cancer, inflammation, and oxidized states caused by reactive oxygen stress (ROS), have been thoroughly researched. Cardiovascular conditions, etc. By employing ethanol and acetic acid to extract its blossom, white frangipani has been shown to have antioxidant activity [33] Extracts from the plant's leaves and flowers show moderate to strong antioxidant activity. The flower and leaf oils had respective total antioxidant capacities (TACs) of 57 µg/g and 83 µg/g. Because leaf extracts include more polyphenols than flower extracts, they often exhibit more DPPH radical scavenging [34].

Gastro protective activity

The methanolic extract produced from the stem bark of Plumeria obtusa was assessed for its gastro protective properties. By suppressing the proton pump mechanism, enhancing gastric mucosal protection, and lowering stomach acid formation, the extract shown effectiveness. [35]

Anti-fungal

Using the conventional dilution test on Mueller-Hinton (MH) agar medium, the antifungal properties of the methanolic extract and the isolated fraction of *P. alba* were assessed. Using the disc diffusion method, the inhibitory zones were compared to those generated by the common antibiotic ciprofloxacin (5 mg/disc). Using Sabouraud dextrose agar medium and the conventional dilution technique, the antifungal impact was also evaluated. The results were compared to the standard antifungal Clotrimazole (125 mcg/ml). [36]

Anti-arthritis

In Sprague-Dawley rats, P. alba's ethyl acetate and n-butanol fractions have antiarthritic effects. P.Alba provides a scientific justification for the plant's traditional use in the treatment of inflammatory diseases such rheumatoid arthritis [37]

Anti- cancer

The fruit of P. alba is regarded as a natural source of antioxidants that help reduce free radical- mediated disorders like diabetes, cancer, and coronary heart disease, and the bark is utilized as a plaster for difficult tumors. [38]

Hepatoprotective

Rats with liver damage caused by paracetamol were used to test the hepatoprotective properties of P. alba extract. Methanol extracts of the plant *P. alba Lam.*, also called *Plumeria acutifolia*, were employed in the study at different concentrations (100, 200, and 400 mg/kg). Poir's efficacy in treating Wistar rats with acute liver injury caused by paracetamol was assessed. At doses up to 2000 mg/kg body weight in mice, the methanolic extract of *P. alba* did not result in any toxic effects or fatalities, suggesting that the extract is safe and non-toxic for additional pharmacological testing. Hepatocytes were arranged neatly and the central vein remained unaltered in the normal control group, which had a typical liver anatomy. [39]

Mechanism of anti-ulcer activity of Plumeria alba

Tannins' ability to chelate metals, antioxidant activity, antibacterial action, and complexation power with other molecules provide the mechanism of action that explains why they enhance the treatment and prevention of diarrhea and gastritis symptoms.[40-43] Excellent antioxidant and anti-inflammatory characteristics of flavonoids contribute in mucosal protection and ulcer healing [44, 45]. Anti-secretory and anti-ulcer effects[46] This class of compounds has become increasingly popular in terms of health protection because it has a remarkable spectrum of biochemical and pharmacological activities. Perhaps the most active area of research with flavonoids today is the possible medicinal contribution that flavonoids make to human health [47]. The main elements of mucosal protection include the generation of cytoprotective prostaglandins (PGs), mucus, bicarbonate (HCO3−), nitric oxide (NO), the endogenous antioxidant system, and adequate blood flow [48,49]. Pepsin activity, bile reflux, hydrochloric acid (HCl) secretion [50], and abnormal motility [51] Kaempferol (40, 80, and 160 mg/kg, p.o.) and the control medication omeprazole (20 mg/kg) avoid gastric ulcers due to ethanol in mice via decreasing neutrophil accumulation, myeloperoxidase (MPO) activity, and pro- inflammatory cytokines consisting of TNF-α, IL-1β, and interleukin-6 (IL-6), and additionally improving NO and gastric mucus [52]. Increased gastric blood flow, improved synthesis of mucosubstances of the gastric mucosa [53], and increased effects on the contents of PGs in gastric tissue [54] are the mechanisms of action involved in gastric protection. In addition to its cytoprotective properties, sofalcone directly inhibits H. pylori with a minimum inhibitory concentration of 55-222 µmol/L, possesses anti-urease action, and decreases the organism's adherence to gastric epithelial cells [55, 56]

CONCLUSION

Plumeria alba L. possesses a wide range of therapeutic characteristics that are supported by both modern pharmacological research and traditional wisdom. It contains a number of bioactive compounds with notable antibacterial, antioxidant, antiarthritic, and analgesic effects. These active metabolites, derived from a variety of plant sources, including alkaloids, flavonoids, tannins, saponins, and polyphenols, serve various functions in ulcer treatment and work in tandem with plant extracts' anti-ulcerative properties. Plumeria alba L. possesses a wide range of therapeutic characteristics that are supported by both modern pharmacological research and traditional wisdom. It contains a number of bioactive compounds with notable antibacterial, antioxidant, antiarthritic, and analgesic effects. The Study’s findings indicate that a certain hydro alcoholic extract of Plumeria alba L. exhibits antiulcer action, as evidenced by the notable reduction of ulcer formation generated by various models, which is in line with the folk medicine literature report.

 

 

REFERENCES

  1. Zatorski H. Pathophysiology and risk factors in peptic ulcer disease. Introd Gastrointest Dis 2017; 2:7–20. Springer.
  2. Narayanan M, Reddy KM, Marsicano E. Peptic Ulcer Disease and Helicobacter pylori infection. Mo Med. 2018 May Jun; 115(3):219-224.
  3. Ocasio Quinones GA, Woolf A. Duodenal Ulcer. [Updated 2023 Apr 17]. In: StatPearls [Internet].    Treasure    Island   (FL):    StatPearls    Publishing; 2023 Available: https://www.ncbi.nlm.nih.gov/b ooks/NBK557390/. 2023; 557390
  4. Ruiz-Hurtado PA, Garduño-Siciliano L, Domínguez-Verano P, Balderas-Cordero D, Gorgua-Jiménez G, CanalesÁlvarez O & Rodríguez-Monroy MA. Propolis and its gastroprotective effects on nsaid-induced gastric ulcer disease: A systematic review. Nutrients, 2021; 13(9): 3169.
  5. Srivastava Y, Kumar V, Srivastava Y & Kumar M. Peptic ulcer disease (PUD), diagnosis, and current medication based management options: schematic overview. Journal of Advances in Medical and Pharmaceutical Sciences, 2023; 25(11): 14-27.
  6. Fisher L, Fisher A, Smith PN (2020) Helicobacter pylori-related diseases and osteoporotic fractures (narrative review). J Clin Med 9(10):3253
  7. J.M. Shin, Y.M. Cho, G. Sachs, Chemistry of covalent inhibition of the gastric (H +, K+)- ATPase by proton pump inhibitors, J. Am. Chem. Soc. 126 (2004) 7800–7811.
  8. J.M. Shin, G. Sachs, Restoration of acid secretion following treatment with proton pump inhibitors, Gastroenterology 123 (2002) 1588–1597.
  9. Jai Moo Shin, Sachs George, Young-moon Cho, Michael Garst, 1- Arylsulfonyl-2- (pyridylmethylsulfinyl) benzimidazoles as new proton pump inhibitor prodrugs, Molecules 14 (12) (2009) 5247–5280.
  10. M.E. Vera, M.L. Mariani, C. Aguilera, A.B. Penissi, Effect of a cytoprotective dose of dehydroleucodine, Xanthatin, and 3-benzyloxymethyl-5 H-furan-2-one on gastric mucosal lesions induced by mast cell activation, Int. J. Mol. Sci. 22 (11) (2021) 5983
  11. Ren J, Jin X, Li J, et al. The global burden of peptic ulcer disease in 204 countries and territories from 1990 to 2019: a systematic analysis for the Global Burden of Disease Study 2019. Int J Epidemiol 2022; 51: 1666–76
  12. Srivastava DP, Rajani GP, Gupta N, Sharma RK, Mandal S. Antiulcer and Anti- inflammatory activity of fresh Leaves Extracts of Polyalthia Long folia In Rats. International Journal of Drug Development & Research 2011; 3(1):351-359.
  13. Tantapakul, C.; Phakhodee, W.; Ritthiwigrom, T.; Yossathera, K.; Deachathai, S.; Laphookhieo, S. Antibacterial compounds from Zanthoxylum rhetsa. Arch. Pharm. Res. 2012, 35, 1139–1142.
  14. Aslam B, Awan T, Javed I, Khaliq T, Khan JA, Raza A. Gastroprotective and antioxidant potential of Glycyrrhiza glabra on experimentally induced gastric ulcers in albino mice. Int J Curr Microbiol App Sci. 2015; 4:451–460.
  15. Ghosh V, Sugumar S, Mukherjee A, Chandrasekaran N. Neem (Azadirachta indica) Oils. In: Essential Oils in Food Preservation, Flavor and Safety. Academic Press; 2016:593–599.
  16. Kim KH, Lee D, Lee HL, Kim CE, Jung K, Kang KS. Beneficial effects of Panax ginseng for the treatment and prevention of neurodegenerative diseases: past findings and future directions. J Ginseng Res. 2018; 42(3):239–247. doi:10.1016/j.jgr.2017.03.011
  17. Sura J, Dwivedi S, Dubey R. Pharmacological, phytochemical, and traditional uses of Plumeria alba LINN. An Indian medicinal plant. SPER J Anal Drug Regul Aff 2016; 1(1):14- 17
  18. Shinde PR, Patil PS, Bairagi VA. Psychopharmacological review of plumeria species. Sch Acad J Pharm. 2014; 3:217–27.
  19. Prajapati ND, Purohit SS. Handbook of Medicinal Plants. Jodhpur, India: Agrobios; 2004. pp. 336–8.
  20. Raju RA. A Textbook of Wild Plants of Indian Subcontinent and Their Economic Use. New Delhi: CBS Publ; 2000. p. 145.
  21. Goyal RK, Goyal G, Goyal S, Mittal S; Pharmacognostical evaluation of bark of Plumeria Shinde PR et al., Sch. Acad. J. Pharm., 2014; 3(2):217-227 226 alba Linn. International Journal of Natural Product Science, 2012; 1: 178
  22. Nargis A, Malik A, Saminanoor A. A new anti-bacterial triterpenoid from Plumeria alba. Fitoterapia 1993; 2:162-6.

 

  1. Rengaswami S, Venkatarao E. Chemical components of Plumeria alba. Proc Indian Acad Sci 1960;52:173-81.
  2. Siddiqui BS, Naeed A, Begum S, Iddiqui S. Minor iridoids from the leaves of Plumeria obtusa. Phytochemistry 1994; 37:769-71. Sura, et al.: Traditional uses of Plumeria alba LINN 4 Journal of Pharmaceutical and BioSciences / Jan-Mar 2018 / Vol 6 | Issue 1
  3. Imrana, M., & Asif, M. (2021). Morphological, ethno botanical, pharmacognostical and pharmacological studies on the medicinal plant Plumeria alba Linn. (Apocynaceae). Arab. J. Med. and Arom. Plants, 6(1), 1–10.
  4. Rakhmawati, A. Antimicrobial Activity and Chemical Composition Analysis of JasminumSambac L. and Plumeria Alba L. Flower Extract strop. J Nat Prod Res 2022, 6 (3), 330-338, doi.org 10.26538
  5. Zahid Z, Khan SW, Patel KA, Konale AG, Lokre S. Antimicrobial activity of essential oil of flowers of Plumeria alba Linn. J Pharm Phytochem Sci 2010; 2:155-7.
  6. Shinde PR, Patil PS, Bairagi VA (2014). Psychopharmacological Review of Plumeria species. Scholars Academic Journal of Pharmacy 3(2):217-227.
  7. Abass S, Parveen R, Irfan M, Malik Z, Husain SA, Ahmad S. Mechanism of antibacterial phytoconstituents: An updated review. Arch Microbiol. (2024) 206:325. doi: 10.1007/s00203- 024-04035-y
  8. Sumeet D, Abhishek D, Dwivedi SN. Folk lore uses of some plants by the tribes of Madhya Pradesh with special reference to their conversation. Ethanol Leaflets 2008; 12:741-3
  9. Liu Y., Wang H., Wei S., Yan Z. Chemical composition and antimicrobial activity of the essential oils extracted by microwave-assisted hydrodistillation from the flowers of two Plumeria species. Analytical Letters. 2012; 45(16):2389–2397.doi: 10.1080/00032719.2012.689905.
  10. Ravichandran Velayudham, Kavimani Subramanyam, and Radha Ramalingum, International Journal of Health Research, June 2008; 1(2): 79-85.
  11. Wrasiati LP, Wirawan IGP, Bagiada NA, Astawa INM (2011). Antioxidant capacity of frangipani (Plumeria alba) Powder Extract. Indonesian Journal of Biomedical Sciences 5(2):1- 11
  12. Mamattah, M. M. et al ,Chemical characterization, antioxidant, antimicrobial, and antibiofilm activities of essential oils of Plumeria alba. Biochem.Res. Int .Vol 2023, 1- 10,Article ID 1040478
  13. Singh, A. P. (2012). Gastroprotective activity of methanolic extract of plumeria obtusa stem bark. . Journal of pharmaceutical and scientific innovation, 26-32.
  14. Shaili Kumari, A. M. (2012). In-vitro antifungal activity of the essential oil of flowers of Plumeria alba Linn. (Apocynaceae). International Journal of PharmTech Research, 208-212.
  15. Chaudhary, M., Kumar, V., Gupta, P., & Singh, S. (2014). Investigation of antiarthritic potential of Plumeria alba L. leaves in acute and chronic models of arthritis. BioMed Res Int.Vol.2014 (1), 474616.
  16. Rudrappa M., Rudayni H. A., Assiri R. A., et al. Plumeria alba-mediated green synthesis of silver nanoparticles exhibits antimicrobial effect and anti-oncogenic activity against glioblastoma U118 MG cancer cell line. Nanomaterials. 2022; 12(3):p. 493. Doi: 10.3390/nano12030493.
  17. Chowdhury, a. r. (2012). Hepatoprotective activity of Plumeria alba extract against paracetamol induced-hepatotoxicity in rats. International Journal of Pharmacy and Pharmaceutical Sciences, 618-620.
  18. Haslam, E., 1989. Plant Polyphenols. Vegetable Tannins Revisited. Cambridge University Press, Cambridge.
  19. Haslam, E., 1996. Natural polyphenols (vegetable tannins) as drugs: possible modes of action. J. Nat. Prod. 59, 205–215.
  20. Haslam, E., Lilley, T.H., Cai, Y., Martin, R., Magnolato, D., 1989. Traditional herbal medicines – the role of polyphenols. Planta Med. 55, 1–8.
  21. Ruggiero, P., Tombola, F., Rossi, G., Pancotto, L., Lauretti, L., Del Giudice, G., Zoratti, M., 2006. Polyphenols reduce gastritis induced by Helicobacter pylori infection or VacA toxin administration in mice. Antimicrob. Agents Chem. 50, 2550–2552.
  22. Khan S., Karmokar A., Howells L., et al. Www.Mnf-Journal.Com page 1 molecular nutrition & food research. 2016; doi: 10.1002/mnfr.201600659.This.
  23. Jo HJ, Kim N, Nam RH, et al. The effect of cochinchina momordica seed extract on gastric acid secretion and morphologic change in aged rat stomach. Gut Liver 2013; 7(5):560– 8. https://doi.org/10.5009/gnl.2013.7.5.560
  24. Mota K.S., Dias G.E., Pinto M.E., Luiz-Ferreira A., Souza-Brito A.R.M., Hiruma-Lima C.A., Barbosa-Filho J.M., Batista L.M. Flavonoids with gastroprotective activity. Molecules. 2009; 14:979–1012. Doi: 10.3390/molecules14030979.
  25. Tungmunnithum D., Thongboonyou A., Pholboon A., Yangsabai A. Flavonoids and Other Phenolic Compounds from Medicinal Plants for Pharmaceutical and Medical Aspects: An Overview. Medicines. 2018; 5:93. Doi: 10.3390/medicines5030093.
  26. Yandrapu H., Sarosiek J. Protective Factors of the Gastric and Duodenal Mucosa: An Overview. Curr. Gastroenterol. Rep. 2015; 17:24. Doi: 10.1007/s11894-015-0452-2.
  27. Galura G.M., Chavez L.O., Robles A., McCallum R. Gastroduodenal Injury: Role of Protective Factors. Curr. Gastroenterol. Rep. 2019; 21:34. Doi: 10.1007/s11894-019-0701-x.
  28. Min C., Hesheng L., Jihong C., Qiaoyun T., Xianzhen L., Chireyeth S. Effects and Mechanism of Changes of Local Neurotransmitters in Rats’ Pylorus and Bile Reflux to the Stomach with Stress Ulcer. Dig.Dis. Sci. 2005; 50:1898-1903. Doi: 10.1007/s10620-005-2958- 1.

 

  1. Kanaizumi T., Nakano H., Matsui T., Tatsumi H., Ishikawa H., Kuramoto H., Shimizu R., Shiratori T. Gastric emptying in patients with gastric and duodenal ulcer. Tohoku J. Exp. Med. 1989; 158:133–140. Doi: 10.1620/tjem.158.133
  2. Li, Q.; Hu, X.; Xuan, Y.; Ying, J.; Fei, Y.; Rong, J.; Zhang, Y.; Zhang, J.; Liu, C.; Liu, Z. Kaempferol protects ethanol-induced gastric ulcers in mice via pro-inflammatory cytokines and NO. Acta Biochim. Biochips Sin. 2018, 50, 246–253.
  3. Saziki, R.; Kyogoku, K.; Hatayama, K.; Suwa, T.; Sawada, J. Anti-ulcer activities of su- 88, a compound related to sophoradin isolated from guang-dou-gen. J. Pharmacobio- Dynam. 1983, 6, S-59.
  4. Saziki, R.; Arai, I.; Isobe, Y.; Hirose, H.; Aihara, H. Effects of sofalcone on necrotizing agents-induced gastric lesions and on endogenous prostaglandins in rat stomachs. J. Pharmacobio-Dynam. 1984, 7, 791–797.
  5. Sunairi, M.; Watanabe, K.; Suzuki, T.; Tanaka, N.; Kuwayama, H.; Nakajima, M. Effects of anti-ulcer agents on antibiotic activity against Helicobacter pylori. Eur J Gastroenterol Hepatol. 1994, 6 (Suppl 1), S121–S124.
  6. Nagate, T.; Numata, K.; Hanada, K.; Kondo, I. The susceptibility of Campylobacter pylori to agents and antibiotics. J Clin Gastroenterol. 1990, 12 (Suppl 1), S135–S138.

Reference

  1. Zatorski H. Pathophysiology and risk factors in peptic ulcer disease. Introd Gastrointest Dis 2017; 2:7–20. Springer.
  2. Narayanan M, Reddy KM, Marsicano E. Peptic Ulcer Disease and Helicobacter pylori infection. Mo Med. 2018 May Jun; 115(3):219-224.
  3. Ocasio Quinones GA, Woolf A. Duodenal Ulcer. [Updated 2023 Apr 17]. In: StatPearls [Internet].    Treasure    Island   (FL):    StatPearls    Publishing; 2023 Available: https://www.ncbi.nlm.nih.gov/b ooks/NBK557390/. 2023; 557390
  4. Ruiz-Hurtado PA, Garduño-Siciliano L, Domínguez-Verano P, Balderas-Cordero D, Gorgua-Jiménez G, CanalesÁlvarez O & Rodríguez-Monroy MA. Propolis and its gastroprotective effects on nsaid-induced gastric ulcer disease: A systematic review. Nutrients, 2021; 13(9): 3169.
  5. Srivastava Y, Kumar V, Srivastava Y & Kumar M. Peptic ulcer disease (PUD), diagnosis, and current medication based management options: schematic overview. Journal of Advances in Medical and Pharmaceutical Sciences, 2023; 25(11): 14-27.
  6. Fisher L, Fisher A, Smith PN (2020) Helicobacter pylori-related diseases and osteoporotic fractures (narrative review). J Clin Med 9(10):3253
  7. J.M. Shin, Y.M. Cho, G. Sachs, Chemistry of covalent inhibition of the gastric (H +, K+)- ATPase by proton pump inhibitors, J. Am. Chem. Soc. 126 (2004) 7800–7811.
  8. J.M. Shin, G. Sachs, Restoration of acid secretion following treatment with proton pump inhibitors, Gastroenterology 123 (2002) 1588–1597.
  9. Jai Moo Shin, Sachs George, Young-moon Cho, Michael Garst, 1- Arylsulfonyl-2- (pyridylmethylsulfinyl) benzimidazoles as new proton pump inhibitor prodrugs, Molecules 14 (12) (2009) 5247–5280.
  10. M.E. Vera, M.L. Mariani, C. Aguilera, A.B. Penissi, Effect of a cytoprotective dose of dehydroleucodine, Xanthatin, and 3-benzyloxymethyl-5 H-furan-2-one on gastric mucosal lesions induced by mast cell activation, Int. J. Mol. Sci. 22 (11) (2021) 5983
  11. Ren J, Jin X, Li J, et al. The global burden of peptic ulcer disease in 204 countries and territories from 1990 to 2019: a systematic analysis for the Global Burden of Disease Study 2019. Int J Epidemiol 2022; 51: 1666–76
  12. Srivastava DP, Rajani GP, Gupta N, Sharma RK, Mandal S. Antiulcer and Anti- inflammatory activity of fresh Leaves Extracts of Polyalthia Long folia In Rats. International Journal of Drug Development & Research 2011; 3(1):351-359.
  13. Tantapakul, C.; Phakhodee, W.; Ritthiwigrom, T.; Yossathera, K.; Deachathai, S.; Laphookhieo, S. Antibacterial compounds from Zanthoxylum rhetsa. Arch. Pharm. Res. 2012, 35, 1139–1142.
  14. Aslam B, Awan T, Javed I, Khaliq T, Khan JA, Raza A. Gastroprotective and antioxidant potential of Glycyrrhiza glabra on experimentally induced gastric ulcers in albino mice. Int J Curr Microbiol App Sci. 2015; 4:451–460.
  15. Ghosh V, Sugumar S, Mukherjee A, Chandrasekaran N. Neem (Azadirachta indica) Oils. In: Essential Oils in Food Preservation, Flavor and Safety. Academic Press; 2016:593–599.
  16. Kim KH, Lee D, Lee HL, Kim CE, Jung K, Kang KS. Beneficial effects of Panax ginseng for the treatment and prevention of neurodegenerative diseases: past findings and future directions. J Ginseng Res. 2018; 42(3):239–247. doi:10.1016/j.jgr.2017.03.011
  17. Sura J, Dwivedi S, Dubey R. Pharmacological, phytochemical, and traditional uses of Plumeria alba LINN. An Indian medicinal plant. SPER J Anal Drug Regul Aff 2016; 1(1):14- 17
  18. Shinde PR, Patil PS, Bairagi VA. Psychopharmacological review of plumeria species. Sch Acad J Pharm. 2014; 3:217–27.
  19. Prajapati ND, Purohit SS. Handbook of Medicinal Plants. Jodhpur, India: Agrobios; 2004. pp. 336–8.
  20. Raju RA. A Textbook of Wild Plants of Indian Subcontinent and Their Economic Use. New Delhi: CBS Publ; 2000. p. 145.
  21. Goyal RK, Goyal G, Goyal S, Mittal S; Pharmacognostical evaluation of bark of Plumeria Shinde PR et al., Sch. Acad. J. Pharm., 2014; 3(2):217-227 226 alba Linn. International Journal of Natural Product Science, 2012; 1: 178
  22. Nargis A, Malik A, Saminanoor A. A new anti-bacterial triterpenoid from Plumeria alba. Fitoterapia 1993; 2:162-6.

 

  1. Rengaswami S, Venkatarao E. Chemical components of Plumeria alba. Proc Indian Acad Sci 1960;52:173-81.
  2. Siddiqui BS, Naeed A, Begum S, Iddiqui S. Minor iridoids from the leaves of Plumeria obtusa. Phytochemistry 1994; 37:769-71. Sura, et al.: Traditional uses of Plumeria alba LINN 4 Journal of Pharmaceutical and BioSciences / Jan-Mar 2018 / Vol 6 | Issue 1
  3. Imrana, M., & Asif, M. (2021). Morphological, ethno botanical, pharmacognostical and pharmacological studies on the medicinal plant Plumeria alba Linn. (Apocynaceae). Arab. J. Med. and Arom. Plants, 6(1), 1–10.
  4. Rakhmawati, A. Antimicrobial Activity and Chemical Composition Analysis of JasminumSambac L. and Plumeria Alba L. Flower Extract strop. J Nat Prod Res 2022, 6 (3), 330-338, doi.org 10.26538
  5. Zahid Z, Khan SW, Patel KA, Konale AG, Lokre S. Antimicrobial activity of essential oil of flowers of Plumeria alba Linn. J Pharm Phytochem Sci 2010; 2:155-7.
  6. Shinde PR, Patil PS, Bairagi VA (2014). Psychopharmacological Review of Plumeria species. Scholars Academic Journal of Pharmacy 3(2):217-227.
  7. Abass S, Parveen R, Irfan M, Malik Z, Husain SA, Ahmad S. Mechanism of antibacterial phytoconstituents: An updated review. Arch Microbiol. (2024) 206:325. doi: 10.1007/s00203- 024-04035-y
  8. Sumeet D, Abhishek D, Dwivedi SN. Folk lore uses of some plants by the tribes of Madhya Pradesh with special reference to their conversation. Ethanol Leaflets 2008; 12:741-3
  9. Liu Y., Wang H., Wei S., Yan Z. Chemical composition and antimicrobial activity of the essential oils extracted by microwave-assisted hydrodistillation from the flowers of two Plumeria species. Analytical Letters. 2012; 45(16):2389–2397.doi: 10.1080/00032719.2012.689905.
  10. Ravichandran Velayudham, Kavimani Subramanyam, and Radha Ramalingum, International Journal of Health Research, June 2008; 1(2): 79-85.
  11. Wrasiati LP, Wirawan IGP, Bagiada NA, Astawa INM (2011). Antioxidant capacity of frangipani (Plumeria alba) Powder Extract. Indonesian Journal of Biomedical Sciences 5(2):1- 11
  12. Mamattah, M. M. et al ,Chemical characterization, antioxidant, antimicrobial, and antibiofilm activities of essential oils of Plumeria alba. Biochem.Res. Int .Vol 2023, 1- 10,Article ID 1040478
  13. Singh, A. P. (2012). Gastroprotective activity of methanolic extract of plumeria obtusa stem bark. . Journal of pharmaceutical and scientific innovation, 26-32.
  14. Shaili Kumari, A. M. (2012). In-vitro antifungal activity of the essential oil of flowers of Plumeria alba Linn. (Apocynaceae). International Journal of PharmTech Research, 208-212.
  15. Chaudhary, M., Kumar, V., Gupta, P., & Singh, S. (2014). Investigation of antiarthritic potential of Plumeria alba L. leaves in acute and chronic models of arthritis. BioMed Res Int.Vol.2014 (1), 474616.
  16. Rudrappa M., Rudayni H. A., Assiri R. A., et al. Plumeria alba-mediated green synthesis of silver nanoparticles exhibits antimicrobial effect and anti-oncogenic activity against glioblastoma U118 MG cancer cell line. Nanomaterials. 2022; 12(3):p. 493. Doi: 10.3390/nano12030493.
  17. Chowdhury, a. r. (2012). Hepatoprotective activity of Plumeria alba extract against paracetamol induced-hepatotoxicity in rats. International Journal of Pharmacy and Pharmaceutical Sciences, 618-620.
  18. Haslam, E., 1989. Plant Polyphenols. Vegetable Tannins Revisited. Cambridge University Press, Cambridge.
  19. Haslam, E., 1996. Natural polyphenols (vegetable tannins) as drugs: possible modes of action. J. Nat. Prod. 59, 205–215.
  20. Haslam, E., Lilley, T.H., Cai, Y., Martin, R., Magnolato, D., 1989. Traditional herbal medicines – the role of polyphenols. Planta Med. 55, 1–8.
  21. Ruggiero, P., Tombola, F., Rossi, G., Pancotto, L., Lauretti, L., Del Giudice, G., Zoratti, M., 2006. Polyphenols reduce gastritis induced by Helicobacter pylori infection or VacA toxin administration in mice. Antimicrob. Agents Chem. 50, 2550–2552.
  22. Khan S., Karmokar A., Howells L., et al. Www.Mnf-Journal.Com page 1 molecular nutrition & food research. 2016; doi: 10.1002/mnfr.201600659.This.
  23. Jo HJ, Kim N, Nam RH, et al. The effect of cochinchina momordica seed extract on gastric acid secretion and morphologic change in aged rat stomach. Gut Liver 2013; 7(5):560– 8. https://doi.org/10.5009/gnl.2013.7.5.560
  24. Mota K.S., Dias G.E., Pinto M.E., Luiz-Ferreira A., Souza-Brito A.R.M., Hiruma-Lima C.A., Barbosa-Filho J.M., Batista L.M. Flavonoids with gastroprotective activity. Molecules. 2009; 14:979–1012. Doi: 10.3390/molecules14030979.
  25. Tungmunnithum D., Thongboonyou A., Pholboon A., Yangsabai A. Flavonoids and Other Phenolic Compounds from Medicinal Plants for Pharmaceutical and Medical Aspects: An Overview. Medicines. 2018; 5:93. Doi: 10.3390/medicines5030093.
  26. Yandrapu H., Sarosiek J. Protective Factors of the Gastric and Duodenal Mucosa: An Overview. Curr. Gastroenterol. Rep. 2015; 17:24. Doi: 10.1007/s11894-015-0452-2.
  27. Galura G.M., Chavez L.O., Robles A., McCallum R. Gastroduodenal Injury: Role of Protective Factors. Curr. Gastroenterol. Rep. 2019; 21:34. Doi: 10.1007/s11894-019-0701-x.
  28. Min C., Hesheng L., Jihong C., Qiaoyun T., Xianzhen L., Chireyeth S. Effects and Mechanism of Changes of Local Neurotransmitters in Rats’ Pylorus and Bile Reflux to the Stomach with Stress Ulcer. Dig.Dis. Sci. 2005; 50:1898-1903. Doi: 10.1007/s10620-005-2958- 1.

 

  1. Kanaizumi T., Nakano H., Matsui T., Tatsumi H., Ishikawa H., Kuramoto H., Shimizu R., Shiratori T. Gastric emptying in patients with gastric and duodenal ulcer. Tohoku J. Exp. Med. 1989; 158:133–140. Doi: 10.1620/tjem.158.133
  2. Li, Q.; Hu, X.; Xuan, Y.; Ying, J.; Fei, Y.; Rong, J.; Zhang, Y.; Zhang, J.; Liu, C.; Liu, Z. Kaempferol protects ethanol-induced gastric ulcers in mice via pro-inflammatory cytokines and NO. Acta Biochim. Biochips Sin. 2018, 50, 246–253.
  3. Saziki, R.; Kyogoku, K.; Hatayama, K.; Suwa, T.; Sawada, J. Anti-ulcer activities of su- 88, a compound related to sophoradin isolated from guang-dou-gen. J. Pharmacobio- Dynam. 1983, 6, S-59.
  4. Saziki, R.; Arai, I.; Isobe, Y.; Hirose, H.; Aihara, H. Effects of sofalcone on necrotizing agents-induced gastric lesions and on endogenous prostaglandins in rat stomachs. J. Pharmacobio-Dynam. 1984, 7, 791–797.
  5. Sunairi, M.; Watanabe, K.; Suzuki, T.; Tanaka, N.; Kuwayama, H.; Nakajima, M. Effects of anti-ulcer agents on antibiotic activity against Helicobacter pylori. Eur J Gastroenterol Hepatol. 1994, 6 (Suppl 1), S121–S124.
  6. Nagate, T.; Numata, K.; Hanada, K.; Kondo, I. The susceptibility of Campylobacter pylori to agents and antibiotics. J Clin Gastroenterol. 1990, 12 (Suppl 1), S135–S138.

Photo
Shipra Mishra
Corresponding author

Department of Pharmacy, Institute of Technology & Management, GIDA, Gorakhpur

Photo
Dr. Suprabha Devi
Co-author

Department of Pharmacy, Institute of Technology & Management, GIDA, Gorakhpur

Shipra Mishra, Dr. Suprabha Devi, A Review: Plumeria alba as an anti-ulcer agent, Int. J. of Pharm. Sci., 2026, Vol 4, Issue 3, 1009-1017. https://doi.org/10.5281/zenodo.18938617

More related articles
A Review of Recent Developments in Drug Delivery...
Sakshi Bhope, Riddhi Shirbhate, Shruti Shende, Sapna Patel, Kamle...
Robotic Surgical Revolution Exploring the Future o...
Ishwari Kiran Shinde , R.S Mohan, R.M Kawade, ...
Polyherbal Gel Formulations for the Management of ...
Arun Shinde, Yashanjali Sabale, Anil Pawar, Ambadas Katarnavare, ...
Adverse Drug Reactions To Anti-Hypertensive: A Hospital Survey Pharmacovigilance...
Sonal Kumbhar , Ayan Noushad Sayyad , Nilesh Chougule , ...
Role of Nutraceuticals in Management of Diabetes Mellitus...
Pratiksha Shinde, Harshada Dhak, Dr. Sonali Uppalwar, ...
Beyond the Leaf: Unlocking the Hidden Power of Aloe vera Flowers...
Purva Salunke, Abhishek Yadav, Sonali Uppalwar, ...
Related Articles
Development of Alcohol-Free Herbal Sanitizer Using Silver Nanoparticles: A Susta...
Nikhil Kadam, Prassanna Bhadange, Vinayak Bhavsar, Vaishnavi Bohade, Yash Bachhav, Ritesh Karmarkar,...
Niosome: as a Novel Pharmaceutical Drug Delivery System...
Rohan Kaswa, Rutuja Kadam, Suyog Kamble, Aboli Kasar, Sakshi Kashid, Manisha Khaire, ...
Comparative Efficacy of Nutraceuticals and Conventional Medicines in Hypertensio...
Arnab Roy, Sajid Ansari, Faiz Alam , Chandan Kumar, Ayush Kumar, Alijan Mansur, Shahid Afridi, Md. A...
UV Method Of Development For Estimation Of Losartan In Bulk & Marketed Formulati...
Pardeshi Jyotshana Gokul, Sonawane Kalyani Amol, Dashpute Sanket Narendra, Wagh Sheetal Vilas , ...
A Review of Recent Developments in Drug Delivery...
Sakshi Bhope, Riddhi Shirbhate, Shruti Shende, Sapna Patel, Kamlesh Wadher, ...
More related articles
A Review of Recent Developments in Drug Delivery...
Sakshi Bhope, Riddhi Shirbhate, Shruti Shende, Sapna Patel, Kamlesh Wadher, ...
Polyherbal Gel Formulations for the Management of Mouth Ulcers: A Critical Revie...
Arun Shinde, Yashanjali Sabale, Anil Pawar, Ambadas Katarnavare, Pratik Sabale, Chaitanya Maharnavar...
A Review of Recent Developments in Drug Delivery...
Sakshi Bhope, Riddhi Shirbhate, Shruti Shende, Sapna Patel, Kamlesh Wadher, ...
Polyherbal Gel Formulations for the Management of Mouth Ulcers: A Critical Revie...
Arun Shinde, Yashanjali Sabale, Anil Pawar, Ambadas Katarnavare, Pratik Sabale, Chaitanya Maharnavar...