Antibacterial Activity Against Foodborne Pathogen and Anti-inflammatory Activity of Caesalpinia sappan Heartwood

Main Article Content

Sumalee Panthong

Abstract

Bacterial foodborne diseases are found all year round in Thailand. Normally, the treatment of such illnesses is primarily supportive; however, antibiotics are considered for severe cases. Caesalpinia sappan (C. sappan) heartwood is used to treat diarrhea by Thai traditional doctors. The aim of this literature review was to gather scientific evidence of the antibacterial and anti-inflammatory effects of C. sappan heartwood and its active compounds; for a better understanding in its mechanisms for the treatment of bacterial foodborne diseases. The results revealed that C. sappan heartwood extracts were capable of inhibiting gram-negative, gram-positive, and antibiotic-resistant bacteria. In addition, C. sappan heartwood showed anti-inflammatory activity against nitric oxide and inflammatory cytokine release. The main compound of C. sappan heartwood is brazilin, which possesses antibacterial and anti-inflammatory activities. Therefore, C. sappan heartwood might be used as an antibacterial and anti-inflammation agent in patients with foodborne diseases.

Article Details

Section
Review Article

References

Division of Epidemiology, Department of Disease Control. Case defnition for communicable diseases surveillance, Thailand, 2020. Nonthaburi: Division of Epidemiology, Department of Control; 2020. (in Thai)

Department of Disease Control. Annual epidemiological surveillance report 2019. [Internet]. 2019 [cited 2022 Mar 30]; Available from: https://ddc.moph.go.th/doe/publishbooksub.php?5 (in Thai)

Sathienluckana T, Pummangura C, Khan-asa B. Treatment guidance of acute diarrhea for community pharmacist. Isan J Pharm Sciences. 2018;14(4):1-17. (in Thai)

Ventola CL. The antibiotic resistance crisis: part 1: causes and threats. P T. 2015;40(4):277-83.

Ekarattanawong S, Sookprasert N, Boonruab J, Bhamarapravati K. Medical plants treatment for diarrhea: from basic science to Thai traditional clinical application. J Med Health Sci. 2018;25(1):127-38.

Martin KW, Ernst E. Herbal medicines for treatment of bacterial infections: a review of controlled clinical trials. J Antimicrob Chemother. 2003;51(2):241-6.

Mazzei R, Leonti M, Spadafora S, Patitucci A, Tagarelli G. A review of the antimicrobial potential of herbal drugs used in popular Italian medicine (1850s-1950s) to treat bacterial skin diseases. J Ethnopharmacol. 2020;250:112443.

Faculty of Pharmacy, Mahidol University. Herbal medicines and local plants (3). Bangkok: Prachachon Company Limited; 1999. (in Thai)

Nirmal NP, Panichayupakaranant P. Antioxidant, antibacterial, and anti-inflammatory activities of standardized brazilin-rich Caesalpinia sappan extract. Pharm Biol. 2015;53(9):1339-43.

Syamsunarno MRA, Safitri R, Kamisah Y. Protective effects of Caesalpinia sappan Linn. and its bioactive compounds on cardiovascular organs. Front Pharmacol. 2021;12:725745.

Bintsis T. Foodborne pathogens. AIMS Microbiol. 2017;3(3):529-63.

Azer SA, Tuma F. Infectious colitis. Treasure Island (FL): StatPearls Publishing; 2022.

Flanagan P, Campbell BJ, Rhodes JM. Bacteria in the pathogenesis of inflammatory bowel disease. Biochem Soc Trans. 2011;39(4):1067-72.

Navaneethan U, Giannella RA. Infectious colitis. Curr Opin Gastroenterol. 2011;27(1):66-71.

Orwa C, Mutua A, Kindt R, Jamnadass R, Anthony S. Agroforestry Database: A Tree Reference and Selection Guide Version 4.0. Kenya: World Agroforestry Centre; 2009.

Zeng K-W, Yu Q, Song F-J, Liao L-X, Zhao M-B, Dong X, Jiang Y, Tu P-F. Deoxysappanone B, a homoisoflavone from the Chinese medicinal plant Caesalpinia sappan L., protects neurons from microglia-mediated inflammatory injuries via inhibition of IκB kinase (IKK)-NF-κB and p38/ERK MAPK pathways. Eur J Pharmacol. 2015;748:18-29.

Zhao M-B, Li J, Shi S-P, Cai C-Q, Tu P-F, Tang L, Zeng K-W, Jiang Y. Two new phenolic compounds from the heartwood of Caesalpinia sappan L. Molecules. 2013;19(1):1-8.

Min BS, Cuong TD, Hung TM, Min BK, Shin BS, Woo MH. Compounds from the heartwood of Caesalpinia sappan and their anti-inflammatory activity. Bioorg Med Chem Lett. 2012;22(24):7436-9.

Xu H-X, Lee SF. The antibacterial principle of Caesalpina sappan. Phytother Res. 2004;18(8):647-51.

Kim K-J, Yu H-H, Jeong S-I, Cha J-D, Kim S-M, You Y-O. Inhibitory effects of Caesalpinia sappan on growth and invasion of methicillin-resistant Staphylococcus aureus. J Ethnopharmacol. 2004;91(1):81-7.

Butkhup L, Samappito S. In vitro Free radical scavenging and antimicrobial activity of some selected Thai medicinal plants. Res J Med Plant. 2011;5(3):254-65.

Rangsipanuratn W, Kummarnjassadakul P, Janwithayanuchita I. Antibacterial activities of ten Thai herbal extracts against Staphylococcus aureus ATCC 25923, Bacillus cereus and Escherichia coli ATCC 25922. HCU Journal. 2016;19(38):35-48.

Nirmal NP, Rajput MS, Prasad RGSV, Ahmad M. Brazilin from Caesalpinia sappan heartwood and its pharmacological activities: a review. Asian Pac J Trop Med. 2015;8(6):421-30.

Xia Z, Li D, Li Q, Zhang Y, Kang W. Simultaneous determination of brazilin and protosappanin B in Caesalpinia sappan by ionic-liquid dispersive liquid-phase microextraction method combined with HPLC. Chem Cent J. 2017;11(1):114.

Mueller M, Weinmann D, Toegel S, Holzer W, Unger FM, Viernstein H. Compounds from Caesalpinia sappan with anti-inflammatory properties in macrophages and chondrocytes. Food Funct. 2016;7(3):1671-9.

Tewtrakul S, Tungcharoen P, Sudsai T, Karalai C, Ponglimanont C, Yodsaoue O. Antiinflammatory and wound healing effects of Caesalpinia sappan L. Phytother Res. 2015;29(6):850-6.

Sireeratawong S, Piyabhan P, Singhalak T, Wongkrajang Y, Temsiririrkkul R, Punsrirat J, Ruangwises N, Saraya S, Lerdvuthisopon N, Jaijoy K. Toxicity evaluation of sappan wood extract in rats. J Med Assoc Thai. 2010;93 Suppl 7:S50-7.

Athinarayanana G, Ranjitsingh AJA, Usha Raja Nanthini A, Padmalatha C. Toxicological studies of Caesalpinia sappan wood derived dye in Wister albino rats. Food Sci Hum Wellness. 2017;6(1):34-8.