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  • Ipomoea Carnea: An In-Depth Pharmacogenetic and Pharmacological Investigation of its Therapeutic Potential and Applications

  • Rungta Institute of Pharmaceutical sciences, Kohka.

Abstract

Ipomea carnea, a plant species in the Convolvulaceae family, has been traditionally used in folk medicine for its health benefits. It has been found to possess antioxidant, anti-inflammatory, antimicrobial, and antifungal properties, making it a potential candidate for treating various diseases. The plant contains bioactive compounds such as alkaloids, flavonoids, and phenolic acids, which exhibit pharmacological activities. Alkaloids, such as argenine and ergometrine, have antioxidant and anti-inflammatory properties, while flavonoids and phenolic acids exhibit antimicrobial and antifungal activities.

Keywords

Antioxidant, Anti-Inflammatory, Antimicrobial

Introduction

Ipomea carnea has therapeutic potential, as it has been traditionally used to treat ailments like fever, rheumatism, and skin diseases. It also has antidiabetic, anticancer, and hepatoprotective properties, making it a potential candidate for treating various diseases. Its antioxidant and anti-inflammatory properties make it a potential candidate for treating neurodegenerative diseases like Alzheimer's and Parkinson's. Hyperlipidemia is a condition where blood lipid levels are high, leading to atherosclerosis, heart attacks, and stroke. It can be inherited or acquired. To manage hyperlipidemia, a healthy lifestyle with proper statins and fibrate medication is essential. Ipomea carnea herbs, native to South Africa, help manage high lipid cholesterol levels and low lipid content. Ayurveda, a traditional Indian medicine, is increasingly used for treating chronic conditions alongside conventional treatments. The safety of Ayurvedic medicines depends on their administration method and individual needs [1]. The medicinal properties of Ipomoea carnea, a shrub with numerous anti-bacterial, anti-fungal, anti-oxidant, anti-cancer, anti-convulsant, immunomodulatory, anti-diabetic, hepatoprotective, anti-inflammatory, anxiolytic, sedative, and wound healing activities. However, it has also been found to have toxicological effects. The major phytochemicals associated with I. carnea's bioactivity could be beneficial for phytotherapy research and drug developmentIpomoea carnea, a plant found in tropical regions, can cause livestock intoxication. The toxic plant's leaves, flowers, and seeds were used to isolate polyhydroxylated alkaloids. Swainsonine, 2-epi-lentiginosine, calystegines B1, B2, B3, and C1 were isolated from the leaf extract. .It is used in Ayurvedic, Siddha, and Unani medical systems as a folk remedy. Ipomea carnea contains chemical components like 2-ethyl-1,3-dimethylbenzene, 2-(12-pentadecynyloxy)tetrahydro2H-pyran, and 3-furanyl[2-hydroxy-4-methyl-2-(2 methylpropyl)cyclopentyl], methanone, 2,2-dideuterooctadecanal, hexadecanoic acid, and linoleic acid[2]. The toxicity of Ipomoea carnea Jacq seeds, an ethnopharmacological drug used by traditional healers. After detoxification using cow's milk, urine, sour gruel, Triphala decoction, and distilled water, Swainsonine was found in all samples, with a new phytoamine detected. The seeds' morpho-anatomical characteristics remained unchanged, possibly due to the detoxification media's antagonist and antidotal action [3].

Benefits of Ipomoea carnea Plant:

1. Anti-inflammatory Properties

2. Antioxidant Activity

3. Antimicrobial Activity

4. Analgesic (Pain-Relieving) Effects

5. Diuretic Properties

6. Antidiabetic Potential

7. Wound Healing and Skin Health

8. CNS (Central Nervous System) Effects

9. Anticancer Properties

10. Hepatoprotective Effects

Plant Description

Ipomoea carnea is a plant that can grow up to six meters tall, but may grow shorter in damp conditions. Its stem expands into a large trunk with thick branches after a year. The plant has simple, petiolate leaves with cylindrical petioles, and alternating leaves that can grow up to 2.75 meters long and 0.5 to 0.8 cm in diameter. The leaves are light green, 10 to 25 cm long, and resemble hearts or lanceolates. Ipomoea carnea's  has strong anti-inflammatory, anti-cancer, anti-sleeping, and anti-cardiovascular qualities.

Fig.1  Ipomea carnea

Botanical Profile Taxonomical Classification

Kingdom: Plantae

Subkingdom: Tracheobionta

Phylum: Spermatophyta

Subphylum: Magnoliophyta

Class: Magnoliopsida– Dicotyledons

Subclass: Asteridae

Order: Solanales

Family: Convolvulaceae

Genus: Ipomoea

Species: Ipomoea carnea

 

MATERIAL AND METHOD

Material and Method

Collection Of Leave

The plant material was collected in the month of August 2024 from Bhilai, Chhattisgarh.

 

Parts of plant

Medicinal properties

Bioactive

Leaves and stems

Analgesic and Sedative

Alkaloids

Leaves

Antioxidants (help in reducing oxidative stress and inflammation) antidiabetic, antimicrobial, and anticancer effects.

Flavonoids

Seeds

Astringent wound healing and antimicrobial effects.

Tannins

Root

Antifungal, antimicrobial, and anti-inflammatory properties.

Saponins

Flower

laxative and diuretic effects

Glycosides

Trunk

Anti-inflammatory and anticancer activities.

Steroids

 

Figure : Ipomea carnea

Identification And Authentication Of Collected Plant

  • Plant parts were identified and authentication was done by Dr. Satyendra Sen Professor Department of Botany, VYT College, Durg (C.G.), 490023.
  • Date – 24/10/2024

Figure : Ipomea carnea for plant authentication

Phytochemical evaluation in ethanolic extract

Ipomea carnea plant samples, either from their natural habitat identify the species using morphological characteristics like leaf shape, flower color, and stem texture. Plant extraction involves harvesting and drying plant material, grinding it into a fine powder, extracting bioactive compounds using a solvent, and then fractionating the extract using techniques like column chromatography or thin-layer chromatography to separate the compounds. This process involves drying the material, grinding it into a powder, and separating the bioactive compounds.

Washing And Shade Drying

Plant samples gathered for preparing undergo a washing process to remove contamination from particles that adhere, such as dust and other contaminants.

Grinding And Sieving

Samples of plant tissue were reduced to the particle size of 0.5 to 1.0 mm to ensure homogeneity and facilitate the destruction of organic matter.

Soxhlet Extraction

The Principle of Soxhlet Extractor

In a thimble made of dense filter paper, which is loaded into the primary chamber of the Soxhlet extractor, solid material comprising some of the required extract is inserted.

Phytochemical Test Evaluation

S.no

Test

Observation

Result

1

Alkaloid

 

 

 

Mayers test

Cream ppt.

+ve

 

Wagner test

Reddish brown

+ve

2

Falavonoids

 

 

 

Shinoda

Yellow

+ve

 

Ferric chloride

Green black ppt

+ve

3

Glycoside

 

 

 

Molisch test

Violet ring formed in between 2 layers

+ve

 

Benedict

Light green

+ve

4

Phenol

 

 

 

Ferric chloride

Greenish black

+ve

 

Lead acetate

Yellow

+ve

5

Amino acid

 

 

 

Ninhydrin

No change

-ve

Phytochemical bioactive compounds in plant –

The chemical structure of compond found on ipomea carneaare swainsonine,calystegine a3,calystegine b1,calystegine b2,calystegine b3,calystegine c1.

 

Phytochemical

Chemical

1 Flavonoids

 

1. Quercetin 2. Kaempferol 3. Isorhapontigenin 

4. Rhapontigenin. 5. Luteolin 6. Apigenin

7. Naringenin. 8. Eriodictyol 9. Taxifolin

2.Tannins

1.Gallic acid. 2. Ellagic acid   3. Catechin. 4. Epicatechin

 5. Gallocatechin         6. Epigallocatechin  7. Tannic acid

8. Chebulagic acid 9. Corilagin 10. Geraniin

3.Saponins

1. Ipomoearasaponin A  2. Ipomoearasaponin B

3. Ipomoearasaponin C  4. Ipomoearasaponin D

 5. Convolvuloside. 6. Convolvuloside A

7. Convolvuloside B 8. Ipomoeasaponin A     

 9. Ipomoeasaponin B

4.Glycosides

1. Ipomoein. 2. Quercetin-3-O-glucoside

 3. Kaempferol-3-O-glucoside  4. Isorhapontigenin-3-O-glucoside  5. Rhapontigenin-3-O-glucoside.

6. Luteolin-7-O-glucoside 7. Apigenin-7-O-glucoside:  8. Naringenin-7-O-glucoside

5.Steroid

1. β-Sitosterol 2. Stigmasterol 3. Campesterol: A phytosterol that has been reported to have antioxidant, anti-inflammatory, and antimicrobial properties.

4. Brassicasterol 5. Ergosterol

The Folin-Ciocalteu and aluminum chloride tests to determine the phenolic and flavonoid contents of Ipomoea carnea Jacq. leaves and flowrutin equivalent (RE) and gallic acid equivalent (GAE) concentrations of 1.336% and 0.885%, respectively. HPLC analysis determined rutin and β-sitosterol concentrations. Ipomoeflavoside, a novel biflavonoid chemical, was isolated from the ethanol extracts showed anticancer, antibacterial, hepatoprotective, antihyperglycemic, and antioxidant properties. The ethanol leaves extract had the strongest cytotoxic effect against breast cancer cell lines[4]. Ipomoea carnea aerial parts, including polyphenols, apigenin-7β-O-glycoside, 3,5-di-O-caffeoylquinic acid, stereoisomers, and scopoletin. GC/MS analysis reveals thirty-three compounds and thirteen alkaloids. The insecticidal potentials of different fractions and isolated compounds were evaluated on Aphis craccivora and Bemisia tabaci, with the alkaloid subfraction being most potent.[5]

Pharmacological Action of Ipomoea Carnea

Cytotoxicity

The  anti-proliferative properties of Indian medicinal plants using the MTT assay. It showed moderate efficacy against HeLa cells at a concentration of 200 µg/ml[6].

CNS

Ipomoea carnea leaf extracts in mice and rats found significant reductions in phenobarbitone-induced sleep time and decreased exploratory activity at doses of 100-400 mg/kg. The extract also prolonged time spent in mazes and increased convulsion onset. The acute toxicity showed a LD50 of 3000 mg/kg, supporting its use in traditional medicine for convulsion and psychosis management[7]. Ipomoea carnea on rat pups and adult offspring. Results showed higher postnatal mortality, smaller size at Day 1, reversible hyperflexion of carpal joints, delay in opening ears, and negative geotaxis in offspring exposed to higher doses. However, no changes were observed in plus-maze, social interaction, forced swimming, catalepsy, stereotyped behavior, or central nervous system monoamine concentrations in adulthood [8].

Antioxidant And Anti-Microbial

In MCF-7 and HpeG2 cell lines were more susceptible to the cytotoxic effects of the leaves' n-butanol component. The maximum antioxidant activity was found in the methanolic extract of the flowers. The leaves' methanolic extract and n-butanol fraction demonstrated higher suggestive antibacterial activity. The study identified new compounds such as β-sitosterol, umbelliferone, kaempferol-3-O-β-D-glucoside, and swainsonine alkaloid[9]. In formulation of  herbal cream (FIHC) with significant antioxidant activity was less toxic to vero cells than A375 cells. The cream reduced sunburn and maintained balanced antioxidant activity in rats exposed to UVB radiation. FIHC accelerated the recovery of UVB-induced lesions through antioxidant and down-regulation of skin photodamage. Taurine's ability to prevent neurotoxicity was also examined, as Ipomoea carnea increased lipid peroxidation markers and disrupted antioxidant homeostasis, leading to elevated levels of TNF, CPK-BB, and LDH. Taurine supplementation could recover oxidative changes and brain damage[10].

Anxiolytic Anticonvulsant

Sedative and anxiolytic effects of leaf extracts at different doses in mice and rats. Results showed that the methanolic and aqueous extracts significantly reduced the time of sleep induced by phenobarbitone, similar to that produced by diazepam. At doses of 100-400 mg/kg, the extract produced a dose-dependent decrease in exploratory activity of mice, with the reduction being greater than that of chlorpromazine.. The LD50 for acute toxicity studies using oral route of administration was 3000 mg/kg[11].

Hypoglycemia

Diabetes is a serious illness with multiple complications and premature mortality, accounting for at least 10% of total health expenditure in many countries. A study investigated the antihyperglycemic effect of Ipomoea carnealeaves in streptozotocin-induced diabetic animals. The leaves were shade dried, powdered, and solvent extracted, and the extracts were administered orally at different doses.  Ipomoea carnealeaves has antihyperglycemic activity in rats, rabbits, and STZ-induced rats. Oral administration of Ipomoea carnealeaves for 21 days significantly reduced blood glucose levels in STZ-induced diabetic rats[12]

Cardiovascular

The cardiac effect of I. carnea's fresh leaves on mouse and frog hearts. The extract blocks the isolated frog heart for 5-10 seconds, followed by a dose-dependent increase in cardiac contractility for up to 2 minutes. Atropine blocks the initial depressant phase and potentiates the stimulant effect. The study suggests that the extract produces a positive inotropic effect on the isolated frog heart, possibly due to sodium extrusion or intracellular calcium release[13]. Cardiovascular function and chemically-induced toxicity. While in vitro analysis cannot replace in vivo experimentation, current methods reduce animal use and provide a better understanding of injury response complexity.[14]. Cardiac effect of Ipomoea carnea leaf extract on frog and mouse hearts. It shows that the extract blocks the heart for 5-10 seconds, then increases cardiac contractility. Atropine blocks the initial depressant phase and intensifies the stimulant effect. The extract's effects aren't affected by propranolol or calcium channel blockers[15].

Antibacterial

The chemical profile of Ipomoea carnea's essential oil (EO) using gas chromatography/mass spectroscopy (GC-MS) . The extracted EO was also aimed at determining its antioxidant and antibacterial activities. 31 compounds were identified, mainly terpenes, with traces of carotenoid and apocarotenoid-derived compounds. The major compounds were tau-cadinol (35.68%), α-cadinol (26.76%), spathulenol (8.11%), and caryophyllene oxide (6.56%). The EO showed significant DPPH and ABTS radical scavenging abilities, and significant inhibition against bacterial growth. Based on these results, I. carnea EO could be used as a potential eco-friendly green resource [16].

Cancer

Cytotoxic, antioxidant, antiproliferative, and polyphenolic qualities. The flower extract made with methanol-distilled water (1:1) had the highest extract recovery (29% w/w) as well as the highest phenolic and flavonoid content. Six polyphenols with the highest antioxidant and reducing potential were identified by HPLC-DAD analysis. The root extract with ethanol and chloroform exhibited the highest level of free radical scavenging [17]. Ehrlich ascites carcinoma in mice. The mice were divided into five groups, with the first group serving as a normal control, the second group as a tumor control, and the third and fourth groups receiving different concentrations of the plant extract. The fourth group received standard fluorouracil for 14 days increases the life span and reduced viable cell counts and ascites fluid volume [18].

Wound Healing

The wound healing mechanisms of Ipomoea carnea, a plant used by Indian tribal groups, using in vitro models. The methanolic extract of I. carnea showed antioxidant, anti-inflammatory, anti-bacterial, and angiogenic activities. It inhibited protein denaturation, protease inhibition, and RBC membrane denaturation. It also showed antibacterial activity on MRSA and controlled its growth rate. The extract improved angiogenic parameters in the CAM model, and increased levels of TNF-alpha and IL-6 were observed in the treated PBMC. This research underscores the potential of plant-based drugs in wound healing[19]. The ethanol extract from Ipomea carnea jacq. leaves affects rat wound healing. The findings revealed improved tensile strength, biochemical parameters, and a notable shrinkage of the wound. The extract ointment contained 0.842% quercetin and had a retention duration of 3.042 minutes. Histopathological analyses revealed a rise in new blood vessels, fibroblasts, and collagen fibers. The leaves' flavonoid and free radical scavenging chemicals may be the cause of the healing effect.[20]

Gastroprotective

An in vivo and in silico study investigated the potential of Ipomoea carnea flower methanolic extract (ICME) as a natural gastroprotective therapy against ethanol-induced gastric ulcers, especially in individuals exposed to ionizing radiation.the Nrf2/HO−1 signaling pathway, which protects the gastrointestinal mucosa from oxidative stress and inflammation.  Phytochemical analysis identified 39 compounds, with flavonoids, hydroxybenzoic acids, and fatty acids as the predominant compounds.[21]

Anti-Inflammatory

The anti-inflammatory properties of Ipomoea carnea leaves, a plant used in India for treating skin diseases. The extracts were tested using carrageenan induced rat paw edema method. The leaves were collected and authenticated, and administered orally at doses of 250 mg/kg and 500 mg/kg body weight. Etocoxib in substitutent 6 group The results showed a significant reduction in paw volume in the test groups (500 mg/kg body weight), indicating the leaves' significant anti-inflammatory properties.[22] The anti-inflammatory and detoxification properties of Ipomoea species, specifically Ipomoea batatas, I. carnea, and I. pescaprae, using phytochemical constituent analysis and toxicity tests on normal and poisoned human cells. Shows high toxicity and detoxification efficacy, with higher cell viability percentages observed when poisoned cells were treated with these extracts. The extracts inhibited VGSCs and VGKCs channels, but not the hERG channel. These plant extracts are used as analgesics, early markers in tumor formation, and treatments for poison and drug addiction. They also exhibit antimicrobial, anti-inflammatory, and antipyretic properties.[23]

The alcoholic extracts of Ipomoea carnea leaves, a plant used in treating skin diseases in India. The extracts were administered orally at doses of 100 mg/kg, 200mg/kg, and 400 mg/kg body weight to five animals. The results showed a significant reduction in paw volume in the test groups (400 mg/kg body weight), indicating that Ipomoea carnea leaves have significant anti-inflammatory activity, as confirmed by the Carrageenan induced paw edema method.[24]

Skin Protective

A The effects of Ipomoea carnea herbal cream on UVB-induced skin damage found that the extract had significant antioxidant activity and less cytotoxicity to vero cells than A375 cells. The cream was tested on rats exposed to UVB radiation and showed reduced sunburn and skin elasticity. Topical application of the cream maintained imbalanced enzyme and non-enzymatic antioxidant activity natural sunscreens can be beneficial in treating inflamed sunburn and dry skin.[25]

Weed

Swainsonine, a cellular glycosidase inhibitor, is poisonous to livestock and Ipomoea species. A study compared the toxicity of calystegines and swainsonine in goats. Goats treated with ground alfalfa, I. carnea, or A. lentiginosus developed clinical disease characterized by mild intention tremors and proprioceptive deficits. A. lentiginosus goats developed disease sooner and with greater consistency. No differences in body weight, serum swainsonine concentrations, or enzyme activity were observed between goats treated with A. lentiginosus and I. carnea[26].

Anti-Diabetic

The antidiabetic properties of Ipomoea carnea and Grewia asiatica leaves on streptozotocin-induced diabetic rats. The leaves were dried, powdered, and extracted, and administered orally at different doses. The results showed that the leaves had hypoglycaemic and antihyperglycemic properties, and significantly reduced blood glucose levels in diabetic rats using the oral glucose tolerance test[27].

Hepatotoxicity

The hepatoprotective potential of Ipomoea carnea leaves in experimental rats. The extract (ICAE) was administered daily for 14 days, and liver injury was induced chemically by CCl4 administration. The hepatoprotective activity was assessed using biochemical parameters and in vivo antioxidant activities significantly prevented chemically induced increases in serum hepatic enzyme levels, reduced lipid peroxidation in liver tissue, and restored defense antioxidant enzyme activities. Histopathology showed ICAE attenuated hepatocellular necrosis and reduced inflammatory cell infiltration[28].

CONCLUSION

Ipomea carnea has revealed its pharmacological properties and therapeutic potential. The plant has antioxidant, anti-inflammatory, antimicrobial, and antifungal properties. The plant contains bioactive compounds like alkaloids, flavonoids, phenols, sterols, tannins, and terpenoids. Its therapeutic potential includes antiidiabetic, anticancer, and hepatoprotective properties. Ipomea carnea has been found to exhibit antioxidant, anti-inflammatory, and antimicrobial activities, making it a potential treatment for various diseases. It also contains bioactive compounds like swainsonine, calystegine B2, and calystegine C1, which are mannosidase inhibitors and glycosidase inhibitors.  The plant's extracts have been found to inhibit the growth of cancer cells and induce apoptosis, protect the liver against damage and disease, protect against neurodegenerative diseases like Alzheimer's and Parkinson's, and reduce blood pressure and improve cardiovascular health. In conclusion, Ipomea carnea's pharmacological properties make it a promising plant species for the development of natural remedies and therapies.

REFRENCES

  1. Kumar S, Dobos GJ, Rampp T. The significance of ayurvedic medicinal plants. Journal of evidence-based complementary & alternative medicine. 2017 Jul;22(3):494-501.
  2. Haraguchi M, Gorniak SL, Ikeda K, Minami Y, Kato A, Watson AA, Nash RJ, Molyneux RJ, Asano N. Alkaloidal components in the poisonous plant, Ipomoea carnea (Convolvulaceae). Journal of Agricultural and food chemistry. 2003 Aug 13;51(17):4995-5000.
  3. Wadnerwar N, Deogade M, Singh M. Pharmacognostical and Pharmaceutical Exploration of the traditional medicine Ipomoea carnea Jacq. International Journal of Ayurvedic Medicine. 2023;14(1):139-44
  4. Kamal AM, Shakour ZT, All SA, Sleem AA, Haggag EG. Phytochemical and biological investigation of Ipomoea carnea Jacq. grown in Egypt. International Journal of Pharmacognosy and Phytochemical Research. 2017;9(2):266-81.
  5. Elhefni MA, El-Rokh AR, El-Rafey HH, Tadros LK, Taher MA. Phytochemical profiling and isolation of bioactive polyphenols from Ipomoea carnea. Egyptian Journal of Chemistry. 2023 Dec 1;66(12):529-43.
  6. Sivajothi V, Shruthi SD, Bhargavi CH, Muthukumar A. Evaluation of in-vitro cytotoxicity of Monochoria vaginalis, Ipomoea carnea, Nardostachys jatamansi extracts on HeLa cells.
  7. Rout SK, Kar DM. Sedative, anxiolytic and anticonvulsant effects of different extracts from the leaves of Ipomoea carnea in experimental animals. Int J Drug Dev Res. 2013 Apr;5(2):232-43.
  8. Schwarz A, Górniak SL, Bernardi MM, Dagli ML, Spinosa HD. Effects of Ipomoea carnea aqueous fraction intake by dams during pregnancy on the physical and neurobehavioral development of rat offspring. Neurotoxicology and teratology. 2003 Sep 1;25(5):615-26.
  9. Hasan M, Ibrahim S, El-Seoud KA, El-Aasr M. Cytotoxic, antioxidant and antimicrobial activities of Ipomoea carnea spp. fistulosa (Mart. ex Choisy) D. Austin. World Journal of Pharmaceutical Sciences. 2015 Jun 2:1217-31
  10. Abou El-khair AR, Ghanem N, Soliman MM, Aldhahrani A, Farag MR, Abd El-Hack ME, Shukry M. Ameliorative impact of taurine on oxidative damage induced by Ipomoea carnea toxicity in wistar male rats through modulation of oxidative stress markers, apoptotic and Nrf2 pathway. Journal of King Saud University-Science. 2021 Dec 1;33(8):101639.
  11. Rout SK, Kar DM. Sedative, anxiolytic and anticonvulsant effects of different extracts from the leaves of Ipomoea carnea in experimental animals. Int J Drug Dev Res. 2013 Apr;5(2):232-43.
  12. Singh RK. Antihyperglycemic Effect of Ipomoea Carnea Leaves in Streptozotocin Induced Diabetic (Master's thesis, Rajiv Gandhi University of Health Sciences (India)).
  13. Bachhav KV, Burande MD, Rangari VD, Mehta JK. Effect of aqueous extract of Ipomoea carnea leaf on isolated frog and mouse heart.
  14. Partridge CR, Johnson CD, Ramos KS. In vitro models to evaluate acute and chronic injury to the heart and vascular systems. Toxicology in vitro. 2005 Aug 1;19(5):631-44.
  15. Bachhav KV, Burande MD, Rangari VD, Mehta JK. Effect of aqueous extract of Ipomoea carnea leaf on isolated frog and mouse heart.
  16. Abd-ElGawad AM, Elshamy AI, Elgorban AM, Hassan EM, Zaghloul NS, Alamery SF, El Gendy AE, Elhindi KM, Ei-Amier YA. Essential oil of Ipomoea carnea: Chemical profile, chemometric analysis, free radical scavenging, and antibacterial activities. Sustainability. 2022 Aug 3;14(15):9504.
  17. Khan MZ, Zahra SS, Ahmed M, Fatima H, Mirza B, Haq IU, Khan SU. Polyphenolic profiling of Ipomoea carnea Jacq. by HPLC-DAD and its implications in oxidative stress and cancer. Natural product research. 2019 Jul 18;33(14):2099-104.
  18. Ramalingam S, Adithiya RA, Joseph A, Saravanan R. Anticancer activity of Ipomoea carnea on Ehrlich ascites carcinoma bearing mice. Indian journal of pharmaceutical Education and Research. 2019 Oct 1;53(4):703-9.
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  20. Shukla R, Gupta G, Kashaw SK, Jain AP, Lodhi S. Wound healing effect of ethanolic extract from Morning Glory (Ipomoea carnea Jacq.) leaves by using different models in rats. Pakistan journal of pharmaceutical sciences. 2018 Jul 1;31(4).
  21. Ghareeb MA, Mohammed HS, Aboushousha T, Lotfy DM, El-Shazly MA, Sobeh M, Taha EF. Ipomoea carnea mitigates ethanol-induced ulcers in irradiated rats via Nrf2/HO− 1 pathway: an in vivo and in silico study. Scientific Reports. 2024 Feb 12;14(1):3469.
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  23. Ameamsri U, Tanee T, Chaveerach A, Peigneur S, Tytgat J, Sudmoon R. Anti-inflammatory and detoxification activities of some Ipomoea species determined by ion channel inhibition and their phytochemical constituents. ScienceAsia. 2021 Jun 1;47(3):321-9.
  24. Mani M, Thakkar N, Kumar P, Verma N, Shukla D. Anti-Inflammatory Activity Of Hydroalcoholic Extract Of Ipomoea Carnea. NeuroQuantology. 2022;20(10):1490.
  25. Sundar M, Lingakumar K. Investigating the efficacy of topical application of Ipomoea carnea herbal cream in preventing skin damage induced by UVB radiation in a rat model. Heliyon. 2023 Sep 1;9(9).
  26. de Carvalho Nunes L, Stegelmeier BL, Cook D, Pfister JA, Gardner DR, Riet-Correa F, Welch KD. Clinical and pathological comparison of Astragalus lentiginosus and Ipomoea carnea poisoning in goats. Toxicon. 2019 Dec 5;171:20-8
  27. Latif AK, Prasad AK, Shankul Kumar SK, Iyer SV, Patel HA, Patel JA. Comparative antidiabetic studies of leaves of Ipomoea carnea and Grewia asiatica on streptozotocin induced diabetic rats.
  28. Gupta RK, Chaudhary SA, Vaishali SR. Antihepatotoxic influence of aqueous extract of Ipomoea carnea against carbon tetrachloride induced acute liver toxicity in experimental rodents. Asian J Pharm Clin Res. 2012;5(4):262-5..

Reference

  1. Kumar S, Dobos GJ, Rampp T. The significance of ayurvedic medicinal plants. Journal of evidence-based complementary & alternative medicine. 2017 Jul;22(3):494-501.
  2. Haraguchi M, Gorniak SL, Ikeda K, Minami Y, Kato A, Watson AA, Nash RJ, Molyneux RJ, Asano N. Alkaloidal components in the poisonous plant, Ipomoea carnea (Convolvulaceae). Journal of Agricultural and food chemistry. 2003 Aug 13;51(17):4995-5000.
  3. Wadnerwar N, Deogade M, Singh M. Pharmacognostical and Pharmaceutical Exploration of the traditional medicine Ipomoea carnea Jacq. International Journal of Ayurvedic Medicine. 2023;14(1):139-44
  4. Kamal AM, Shakour ZT, All SA, Sleem AA, Haggag EG. Phytochemical and biological investigation of Ipomoea carnea Jacq. grown in Egypt. International Journal of Pharmacognosy and Phytochemical Research. 2017;9(2):266-81.
  5. Elhefni MA, El-Rokh AR, El-Rafey HH, Tadros LK, Taher MA. Phytochemical profiling and isolation of bioactive polyphenols from Ipomoea carnea. Egyptian Journal of Chemistry. 2023 Dec 1;66(12):529-43.
  6. Sivajothi V, Shruthi SD, Bhargavi CH, Muthukumar A. Evaluation of in-vitro cytotoxicity of Monochoria vaginalis, Ipomoea carnea, Nardostachys jatamansi extracts on HeLa cells.
  7. Rout SK, Kar DM. Sedative, anxiolytic and anticonvulsant effects of different extracts from the leaves of Ipomoea carnea in experimental animals. Int J Drug Dev Res. 2013 Apr;5(2):232-43.
  8. Schwarz A, Górniak SL, Bernardi MM, Dagli ML, Spinosa HD. Effects of Ipomoea carnea aqueous fraction intake by dams during pregnancy on the physical and neurobehavioral development of rat offspring. Neurotoxicology and teratology. 2003 Sep 1;25(5):615-26.
  9. Hasan M, Ibrahim S, El-Seoud KA, El-Aasr M. Cytotoxic, antioxidant and antimicrobial activities of Ipomoea carnea spp. fistulosa (Mart. ex Choisy) D. Austin. World Journal of Pharmaceutical Sciences. 2015 Jun 2:1217-31
  10. Abou El-khair AR, Ghanem N, Soliman MM, Aldhahrani A, Farag MR, Abd El-Hack ME, Shukry M. Ameliorative impact of taurine on oxidative damage induced by Ipomoea carnea toxicity in wistar male rats through modulation of oxidative stress markers, apoptotic and Nrf2 pathway. Journal of King Saud University-Science. 2021 Dec 1;33(8):101639.
  11. Rout SK, Kar DM. Sedative, anxiolytic and anticonvulsant effects of different extracts from the leaves of Ipomoea carnea in experimental animals. Int J Drug Dev Res. 2013 Apr;5(2):232-43.
  12. Singh RK. Antihyperglycemic Effect of Ipomoea Carnea Leaves in Streptozotocin Induced Diabetic (Master's thesis, Rajiv Gandhi University of Health Sciences (India)).
  13. Bachhav KV, Burande MD, Rangari VD, Mehta JK. Effect of aqueous extract of Ipomoea carnea leaf on isolated frog and mouse heart.
  14. Partridge CR, Johnson CD, Ramos KS. In vitro models to evaluate acute and chronic injury to the heart and vascular systems. Toxicology in vitro. 2005 Aug 1;19(5):631-44.
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Photo
Dr. Bhumika Chandrakar
Corresponding author

Rungta Institute of Pharmaceutical sciences, Kohka.

Photo
Laxmi Athbhaiya
Co-author

Rungta Institute of Pharmaceutical sciences, Kohka.

Laxmi Athbhaiya, Dr. Bhumika Chandrakar*, Ipomoea Carnea: An In-Depth Pharmacogenetic and Pharmacological Investigation of its Therapeutic Potential and Applications, Int. J. of Pharm. Sci., 2025, Vol 3, Issue 3, 385-395. https://doi.org/10.5281/zenodo.14989477

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