Hepatoprotective and Antioxidant Activity of a Mangrove Plant Lumnitzera Racemosa
Overview
Affiliations
Objective: To identify the hepatoprotective and in vitro antioxidant activity of Lumnitzera racemosa (L. racemosa) leaf extract.
Methods: Animals in Group 1 served as vehicle control, Group 2 served as hepatotoxin (CCL4 treated) group, Group 3 served as positive control (Silymarin) group, and Group 4, 5 and 6 served as (75, 150 and 300 mg/kg bw p.o.) L. racemosa leaf extract treated groups. Moreover, in vitro antioxidant DPPH, hydroxyl radical scavenging activity (HRSA), NO, ferric reducing antioxidant power (FRAP), lipid hydroperoxide (LPO) and super oxide dismutase (SOD) were also analyzed for the leaf extract.
Results: The levels of the serum parameters such as serum glutamic oxaloacetic transaminase (SGOT), serum glutamic pyruvic transaminase (SGPT), alkaline phosphatase (ALP), bilirubin, cholesterol (CHL), sugar and lactate dehydrogenase (LDH) were significantly increased in CCL4 treated rats when compared with the control group (P<0.05). But the L. racemosa leaf extract treated rats showed maximum reduction of SGOT [(210.36±19.63) IU/L], SGPT [(82.37±13.87) IU/L], ALP [(197.63±23.43) IU/L], bilurubin [(2.15±0.84) mg/dL], cholesterol [(163.83±15.63) mg/dL], sugar [(93.00±7.65) mg/dL] and LDH [(1134.00±285.00) IU/L] were observed with the high dose (300 mg/kg bw) of leaf extract treated rats. Histopathological scores showed that, no visible changes were observed with high dose (300 mg/kg bw) of leaf extract treated rats except few mild necrosis. The IC50 values were observed as (56.37±4.87) µg/mL, (57.68±1.98) µg/mL, (64.15±2.90) µg/mL, (61.94±3.98) µg/mL, (94.53±1.68) µg/mL and (69.7±2.65) µg/mL for DPPH, HRSA, NO, FRAP, LPO and SOD radical scavenging activities, respectively.
Conclusions: In conclusion, the hepatoprotective effect of the L. racemosa leaf extract might be due to the presence of phenolic groups, terpenoids and alkaloids and in vitro antioxidant properties.
Gadhoumi H, Dhouafli Z, Yeddes W, Serairi Beji R, Miled K, Trifi M Indian J Microbiol. 2024; 64(1):229-243.
PMID: 38468731 PMC: 10924858. DOI: 10.1007/s12088-023-01172-8.
Kappen J, Manurung J, Fuchs T, Vemulapalli S, Schmitz L, Frolov A Mar Drugs. 2023; 21(4).
PMID: 37103381 PMC: 10144801. DOI: 10.3390/md21040242.
Ayenew K, Wasihun Y BMC Complement Med Ther. 2023; 23(1):99.
PMID: 37005601 PMC: 10067186. DOI: 10.1186/s12906-023-03931-y.
Inhibits PCSK9 and Lowers Cholesterol Levels in Rats.
Kamaruddin N, Hajri N, Andriani Y, Abdul Manan A, Tengku Muhammad T, Mohamad H Molecules. 2021; 26(16).
PMID: 34443682 PMC: 8398678. DOI: 10.3390/molecules26165094.
Pangestika I, Oksal E, Tengku Muhammad T, Amir H, Syamsumir D, Abdul Wahid M Saudi J Biol Sci. 2020; 27(8):1947-1960.
PMID: 32714018 PMC: 7376234. DOI: 10.1016/j.sjbs.2020.06.010.