Chemical composition and wound healing potential of Lindernia ruellioides (Colsmann) Pennell from Mizoram, India

C Lalthansangi , RK Lalremtluangi , Esther Lalhmingliani

Asian Pacific Journal of Tropical Biomedicine ›› 2025, Vol. 15 ›› Issue (4) : 169 -176.

PDF (790KB)
Asian Pacific Journal of Tropical Biomedicine ›› 2025, Vol. 15 ›› Issue (4) : 169 -176. DOI: 10.4103/apjtb.apjtb_22_25
Original Article

Chemical composition and wound healing potential of Lindernia ruellioides (Colsmann) Pennell from Mizoram, India

Author information +
History +
PDF (790KB)

Abstract

Objective: To explore the wound healing potential and chemical components of Lindernia ruellioides from Mizoram, India.

Methods: Plant extraction was conducted by cold maceration using chloroform, ethanol, and distilled water as solvents. To guarantee the safety of the plant extract, an acute dermal toxicity test was conducted before the experiment. Antioxidant assays were performed. Excision and incision wound models were used to assess the wound healing activities, including wound closure rate, epithelialization period, and tensile strength. A histopathological examination was carried out.

Results: Lindernia ruellioides contained bioactive compounds, such as mycolactone F, 1-O-octadec-9-enyl glycerol, reserpine, tetracosanoic acid, 2-O-caffeoylglucarate and several others which are found to possess various pharmacological activities. Acute dermal toxicity evaluation showed that the doses were deemed safe. Ethanol extract of Lindernia ruellioides (LREE) treatment significantly elevated glutathione, glutathione-S-transferase, and superoxide dismutase, and decreased malondialdehyde in a dose- dependent manner. It showed increased wound contraction rate, shorter epithelialization time, and elevated wound breaking strength in the LREE-treated group when compared with the control. In addition, the histological examination showed enhanced neovascularization, fibroblasts, and collagen in LREE-treated animals.

Conclusions: Lindenia ruellioides exhibits remarkable effects on wound healing. The study validates the traditional use of this plant in Mizoram region as a wound-healing agent.

Keywords

Lindenia ruellioides / Ethanolic extract / LC-MS / Antioxidant / Wound healing

Cite this article

Download citation ▾
C Lalthansangi, RK Lalremtluangi, Esther Lalhmingliani. Chemical composition and wound healing potential of Lindernia ruellioides (Colsmann) Pennell from Mizoram, India. Asian Pacific Journal of Tropical Biomedicine, 2025, 15(4): 169-176 DOI:10.4103/apjtb.apjtb_22_25

登录浏览全文

4963

注册一个新账户 忘记密码

Conflict of interest statement

The authors declare that there is no conflict of interest.

Funding

The authors received no extramural funding for the study.

Data availability statement

The data supporting the findings of this study are available from the corresponding author upon request.

Authors’ contributions

CL contributed to designing the experiment, data curation, investigation, writing the manuscript, and reviewing and editing the manuscript. RKL assisted with the experiment. EL was involved in supervision, and conceptualization as well as provided lab equipment and chemicals. The final manuscript was read and approved by all of the authors.

Publisher’s note

The Publisher of the Journal remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

[1]

Gupta A. Classification of wounds and the physiology of wound healing. In: Kumar P, Kothari V (eds.) Wound healing research. Singapore: Springer; 2021, p. 3-53.

[2]

Subramoniam A, Evans DA, Rajasekharan S, Nair GS. Effect of Hemigraphis colorata (Blume) H. G. Hallier leaf on wound healing and inflammation in mice. Ind J Pharmacol 2001; 33(4): 283-285.

[3]

Bairy KL, Rao CM. Wound healing profiles of Ginkgo biloba. J Nat Remedies 2001; 1(1): 25-27.

[4]

Talbott HE, Mascharak S, Griffin M, Wan DC, Longaker MT. Wound healing, fibroblast heterogeneity, and fibrosis. Cell Stem Cell 2022; 29(8): 1161-1180.

[5]

Ghosh A. Comparison of wound healing activity of Jethimadh with Triphala in rats. Int J Health Allied Sci 2012; 1(2): 59-63.

[6]

Niknam S, Tofighi Z, Faramarzi MA, Abdollahifar MA, Sajadi E, Dinarvand R, et al. Polyherbal combination for wound healing: Matricaria chamomilla L. and Punica granatum L. Daru 2021; 29(1): 133-145.

[7]

Cook CDK. Aquatic and Wetland plants of India:A reference book and identification manual for the vascular plants found in permanent or seasonal fresh water in the subcontinent of India South of the Himalayas. 1st ed. New York, Oxford: University Press Inc; 1996, p. 358-359.

[8]

Wei JC, Wang PC, Zhou XL, Tang K, Luo Q, Xu Q, et al. The caffeoyl phenylethanoid glycosides from Lindernia ruellioides and their anti-HBV effects. J Asian Nat Prod Res 2017; 20(8): 757-762.

[9]

Sikdar M, Dutta U. Traditional phytotherapy among the Nath People of Assam. Ethno Med 2008; 2(1): 39-45.

[10]

Rai PK, Lalramnghinglova H. Ethnomedicinal plant resources of Mizoram, India: Implication of traditional knowledge in health care system. Ethnobot Leaflets 2010; 14: 274-305.

[11]

OECD guideline 402. OECD guideline for testing of chemicals Acute dermal toxicity. Paris: OECD Publishing; 1987.

[12]

Lalthansangi C, Lalremtluangi RK, Lalhmingliani E, Vabeiryureilai M. Evaluation of the free radical scavenging activities and antibacterial activities of the extracts of Lindernia ruellioides (Colsmann) Pennell. Curr Trends Biotechnol Pharm 2024; 18(4): 2036-2047.

[13]

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951; 193(1): 265-275.

[14]

Moron MS, Depierre JW, Mannervik B. Levels of glutathione, glutathione reductase and glutathione-s-transferase activities in rat lung and liver. Biochim Biophys Acta 1979; 582(1): 67-78.

[15]

Beutler E. Red cell metabolism:A manual of biochemical methods. 3rd ed. New York, USA: Grune and Stratton Inc; 1984, p. 175-195.

[16]

Fried R. Enzymatic and non-enzymatic assay of superoxide dismutase. Biochimie 1975; 57(5): 657-660.

[17]

Beuege JA, Aust SD. Microsomal lipid peroxidation. Methods Enzymol 1978; 30: 302-310.

[18]

Morton JJ, Malone MH. Evaluation of vulneray activity by an open wound procedure in rats. Arch Int Pharmacodyn Ther 1972; 196(1): 117-126.

[19]

Kamath JV, Rana AC, Chowdhury AR. Pro-healing effect of Cnnamomum zeylanicum bark。 Phytother Res 2003; 17(8): 970-972.

[20]

Werner S, Breeden M, Hubner G, Greenhalgh DG, Longaker MT. Induction of keratinocyte growth factor expression is reduced and delayed during wound healing in the genetically diabetic mouse. J Invest Dermatol 1994; 103(4): 469-473.

[21]

Nayak BS, Anderson M, Pereire LMP. Evaluation of wound-healing potential of Catharanthus roseus leaf extract in rats. Fitoterapia 2007; 78(7-8): 540-544.

[22]

Ehrlich HP, Hunt TK. Effects of cortisone and vitamin A on wound healing. Ann Surg 1968; 167(3): 324-328.

[23]

Lee KH. Studies on mechanism of action of salicylate II. Retardation of wound healing by aspirin. J Pharm Sci 1968; 57(6): 1042-1043.

[24]

Bancroft JD, Gamble M. Theory and practice of histological techniques. In: Spencer LT, Bancroft JD (eds.) Tissue processing. 6th ed. Churchill Livingstone: Elsevier; 2008, p. 83-92.

[25]

Chinko BC, Precious-Abraham AD. Wound healing activity of hydromethanolic Dioscorea bulbifera extract on male wistar rat excision wound models. Pharmacol Res- Modern Chin Med 2024; 11: 100425.

[26]

Movaffagh J, Khatib M, Bazzaz BSF, Taherzadeh Z, Hashemi M, Moghaddam AS, et al. Evaluation of wound-healing efficiency of a functional Chitosan/Aloe vera hydrogel on the improvement of re- epithelialization in full thickness wound model of rat. J Tissue Viability 2022; 31(4): 649-656.

[27]

Park EH, Chun MJ. Wound healing activity of Opuntia ficus-indica. Fitoterapia 2001; 72(2): 165-167.

[28]

Nagappa AN, Cheriyan B. Wound healing activity of the aqueous extract of Thespesia populnea fruit. Fitoterapia 2001; 72(5): 503-506.

[29]

Dissemond J, Goos M, Wagner SN. The role of oxidative stress in the pathogenesis and therapy of chronic wounds. Hautarzt 2002; 53(11): 718-723.

[30]

Nayak BS, Sandiford S, Maxwell A. Evaluation of the wound-healing activity of ethanolic extract of Morinda citrifolia L. leaf. Evid Based Complement Alternat Med 2009; 6(3): 351-356.

[31]

Tsuchiya H, Sato M, Miyazaki T, Fujiwara S, Tanigaki S, Ohyama M, et al. Comparative study on the antibacterial activity of phytochemical flavanones against methicillin-resistant Staphylococcus aureus. J Ethnopharmacol 1996; 50(1): 27-34.

[32]

Shetty S, Udupa S, Udupa L. Evaluation of antioxidant and wound healing effects of alcoholic and aqueous extract of Ocimum sanctum Linn in rats. Evid Based Complement Alternat Med 2008; 5(1): 95-101.

[33]

Moyer KE, Saggers GC, Allison GM, Mackay DR, Ehrlich HP. Effects of interleukin-8 on granulation tissue maturation. J Cell Physiol 2002; 193(2): 173-179.

[34]

Ahad HA, Suma Padmaja B, Sravanthi M, Ramyasree P, Kavitha K. Phytochemical screening and anti-inflammatory actions of Alangium salviifolium root extract. Nat Prod Res 2012; 26(17): 1649-1653.

[35]

Lawal B, Sani S, Onikanni AS, Ibrahim YO, Agboola AR, Lukman HY, et al. Preclinical anti-inflammatory and antioxidant effects of Azanza garckeana in STZ-induced glycemic-impaired rats, and pharmacoinformatics of it major phytoconstituents. Biomed Pharmacother 2022; 152: 113196.

[36]

Guenin-Macé L, Baron L, Chany AC, Tresse C, Saint-Auret S, Jönsson F, et al. Shaping mycolactone for therapeutic use against inflammatory disorders. Sci Transl Med 2015; 7(289): 289ra85.

[37]

Vallée M. Neurosteroids and potential therapeutics: Focus on pregnenolone. J Steroid Biochem Mol Biol 2016; 160: 78-87.

[38]

Morsy MA, Abdel-Gaber SA, Mokhemer SA, Kandeel M, Sedik WF, Nair AB, et al. Pregnenolone inhibits doxorubicin-induced cardiac oxidative stress, inflammation, and apoptosis-role of matrix metalloproteinase 2 and NADPH oxidase 1. Pharmaceuticals (Basel) 2023; 16(5): 665.

AI Summary AI Mindmap
PDF (790KB)

289

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/