|Year : 2022 | Volume
| Issue : 1 | Page : 20-25
Gum resin extract of Boswellia serrata attenuates lipopolysaccharide-induced inflammation and oxidative damage in hepatic and renal tissues of rats
Narges Marefati1, Farimah Beheshti2, Poorya Etemadizadeh1, Mahmoud Hosseini3, Akbar Anaeigoudari4
1 Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
2 Neuroscience Research Center; Department of Physiology, School of Paramedical Sciences, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran
3 Division of Neurocognitive Sciences, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
4 Department of Physiology, School of Medicine, Jiroft University of Medical Sciences, Jiroft, Iran
|Date of Submission||29-Aug-2021|
|Date of Decision||22-Sep-2021|
|Date of Acceptance||12-Nov-2021|
|Date of Web Publication||31-Dec-2021|
Department of Physiology, School of Medicine, Jiroft University of Medical Sciences, Jiroft
Source of Support: None, Conflict of Interest: None
Objective: To explore the effect of ethyl acetate gum resin extract of Boswellia serrata on lipopolysaccharide (LPS) induced inflammation and oxidative damage in hepatic and renal tissues of rats.
Methods: The rats were divided into four groups: control, LPS, LPS+Boswellia serrata extracts (100 mg/kg and 200 mg/kg). LPS (1 mg/kg) and the extract (100 and 200 mg/kg, 30 min before LPS) were administered intraperitoneally for 3 weeks. The levels of liver enzymes, albumin, total protein, creatinine, blood urea nitrogen (BUN), interleukin (IL)-6, malondialdehyde (MDA), and total thiol groups and superoxide dismutase (SOD) and catalase (CAT) activities were measured.
Results: The levels of liver enzymes, creatinine, and BUN, IL-6, MDA in the LPS group were markedly increased (P<0.001) while albumin, total protein, and total thiol concentration, as well as SOD and CAT activities, were decreased compared with the control group (P<0.05 or 0.01). Boswellia serrata extracts diminished the levels of liver enzymes, creatinine, BUN, IL-6, and MDA (P<0.01 and P<0.001), and elevated the concentration of total protein and total thiol and SOD and CAT activities (P<0.05 or 0.01).
Conclusions: The ethyl acetate gum resin extract of Boswellia serrata reduces LPS-induced inflammatory reactions and oxidative damage, thus ameliorating hepatic and renal function.
Keywords: Boswellia serrata; Lipopolysaccharide; Inflammation; Oxidative stress; Renal function; Hepatic function
|How to cite this article:|
Marefati N, Beheshti F, Etemadizadeh P, Hosseini M, Anaeigoudari A. Gum resin extract of Boswellia serrata attenuates lipopolysaccharide-induced inflammation and oxidative damage in hepatic and renal tissues of rats. Asian Pac J Trop Biomed 2022;12:20-5
|How to cite this URL:|
Marefati N, Beheshti F, Etemadizadeh P, Hosseini M, Anaeigoudari A. Gum resin extract of Boswellia serrata attenuates lipopolysaccharide-induced inflammation and oxidative damage in hepatic and renal tissues of rats. Asian Pac J Trop Biomed [serial online] 2022 [cited 2023 Jun 4];12:20-5. Available from: https://www.apjtb.org/text.asp?2022/12/1/20/333210
There is no study about the effect of ethyl acetate gum resin extract of Boswellia serrata on LPS-stimulated hepatic and renal injuries. The findings of present study demonstrated that this extract alleviated LPS-caused hepatic and renal damage through reducing the level of IL-6 and MDA and enhancing the concentration of antioxidant indexes including total thiol groups and the activity of SOD and CAT.
| 1. Introduction|| |
Inflammation and oxidative stress participate in the pathogenesis of liver and kidney injuries. Contact of immune cells, especially macrophages with inflammatory stimuli including bacterial endotoxins, results in excessive generation of inflammatory mediators and free radicals. Tumor necrosis factor-alpha (TNF-α) and interleukin (IL)- 6 are inflammatory mediators causing liver and kidney destruction via programmed cell death. It has been detected that the level of inflammatory mediators such as TNF-α remarkably increased in patients with hepatic cirrhosis associated with renal failure. In addition, uncontrolled release of oxidant agents including hydrogen peroxidase and superoxide anion from the Kupffer cells has been propounded to have a central role in hepatic damages. Accumulation of reactive oxygen species in the kidney tissue has been also considered as an important cause in induction of kidney injuries by triggering the inflammatory reactions and destruction of glomerular filtration barrier,.
Gram-negative bacteria cell wall possesses a toxic particle that is named lipopolysaccharide (LPS). This active bacterial endotoxin has been demonstrated to boost the release of inflammatory mediators causing oxidative stress. LPS has been found to impair liver circulation and induce hepatic cell necrosis. It has been reported that TNF-α released from LPS-exposed Kupffer cells disturbs normal liver function through the induction of hepatocyte apoptosis. The hurtful effects of accumulation of TNF-α induced by LPS on kidney function have been also confirmed. Additionally, it has been documented that employment of anti-TNF-α antibodies could improve renal dysfunction caused by LPS.
Use of medicinal plants and derived compounds from them has been recognized as a beneficial strategy in reduction of destructive effects of inflammation and oxidative stress on body tissues. Gum resin of Boswellia serrata (B. serrata) has been employed as an effective remedy in treatment of different ailments in traditional medicine. It has been indicated that boswellic acids presented in the extract of B. serrata could suppress the biosynthesis of inflammatory cytokines. Oleo-gum resin of B. serrata has been revealed to protect the liver tissue against carbon tetrachloride (CCl4)-induced toxicity through the amplification of antioxidant capacity and suppression of inflammatory factors such as nuclear factor κB (NF-κB), IL-6, TNF-α and transforming growth factor-β (TGF-β). In addition, researchers reported that B. serrata extract could augment the activity of antioxidant enzymes including catalase (CAT) and superoxide dismutase (SOD). These effects were attributed to the presence of the triterpenes in the extract of this medicinal plant. This study aimed to evaluate the effect of ethyl acetate gum resin extract of B. serrata on LPS-induced inflammation and oxidative damage in hepatic and renal tissues of rats.
| 2. Materials and methods|| |
2.1. Animals and groups
A total of 32 adult male Wistar rats in the weight range of 200-250 g were procured from the animal nest of Mashhad University of Medical Sciences, Mashhad, Iran. The rats were housed in Plexiglas cages at ambient temperature at (20 ± 2) °C and maintained on a 12-hour light/dark cycle. The rats were allowed to use adequate water and food and randomly divided into four groups (n = 8 rats per group) as follows: control group (1 mL of saline), LPS group (1 mg/kg LPS), LPS+extract (100 mg/kg) and LPS+extract (200 mg/kg). In two treatment groups, the rats were treated with 100 and 200 mg/kg of ethyl acetate gum resin extract of B. serrata, respectively, 30 min before LPS. Treatments were executed intraperitoneally for 3 weeks. At the end of experiment, blood samples were taken from the heart of rats for measurement of alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), albumin, total protein, creatinine, and blood urea nitrogen (BUN). After that, liver and kidney tissues were collected for detection of the concentration of interleukin (IL)-6, malondialdehyde (MDA), and total thiol groups and activities of SOD and CAT.
2.2. Preparation of ethyl acetate gum resin extract of B. serrata
In the current study, the gum resin of B. serrata was used. After identification of the plant by a botanist, a voucher specimen (E-1330 FUMH) was deposited at the Herbarium of Ferdowsi University of Mashhad, Mashhad, Iran. Preparation of ethyl acetate extract was started with comminuting and dissolving 100 g of gum resin in 400 mL of ethyl acetate. The prepared mixture was stirred at 38 °C for 48 h. After filtration, the solvent was removed completely using a rotary apparatus at 40 °C. Then the extract was dissolved in dimethyl sulfoxide and saline for further experiment.
2.3. Assessment of liver and kidney function indices
For assessment of liver function indicators (ALT, AST, ALP, albumin, total protein) and kidney function markers (creatinine and BUN), the serum was isolated from blood samples by centrifuging at 3 500 rpm for 15 min. Then serum samples were used for detection of liver and kidney indices.
2.4. Detection of IL-6 concentration
IL-6 concentration in the liver and kidney tissues was detected using an ELISA kit. For this purpose, filled plates of 100 μL of samples were housed at room temperature. Plates were then kept in a dark enviroment for 1 h after draining and adding biotin-antibody. After that, plates were re-incubated for 1 h in the presence of HRP- avidin. After washing 5 times, substrate-TMB was employed for 15 min and finally, the absorbance was recorded at 450 nm by an ELISA reader.
2.5. Evaluation of oxidative stress indices
2.5.1. MDA detection
MDA level of liver and kidney samples was assessed by thiobarbituric acid. Combination of thiobarbituric acid with MDA generated a color complex with a peak absorbance at 535 nm. In this colorimetric method, the level of MDA was presented in nanomol/g tissue.
2.5.2. Determination of total thiol groups
For determination of total thiol groups, 50 μL of samples, 0.5 mL of tris–EDTA buffer, and 40 μL of DTNB (10 mM) were mixed. After keeping at room temperature for 20 min, the absorbance of the color complex was calculated at 412 nm.
2.5.3. Determination of SOD activity
Assessment of SOD activity was implemented based on autoxidation of pyrogallol. In this colorimetric method, superoxide resulted from autoxidation of pyrogallol inhibits the reduction of tetrazolium dye MTT to formazan. The SOD activity was measured at 570 nm.
2.5.4. Determination of CAT activity
For measurement of CAT activity, Aebi’s method was employed. Briefly, the substrate of CAT, hydrogen peroxide (H2O2), was added to specimens and absorbance was computed. Decline in absorbance was considered as a sign of the decomposition of H2O2 into O2 and H2O by CAT.
2.6. Statistical analysis
Statistical analysis was carried out using SPSS20.0 software. The results were presented as mean ± standard deviation (SD). Analysis of data was achieved by one-way ANOVA followed by Tukey’s test. P<0.05 was considered significantly different.
2.7. Ethical statement
The experiment complied with Recommendations of the Ethical Committee of Jiroft University of Medical Sciences (IR.JMU. REC.1400.002, 2021).
| 3. Results|| |
3.1. Effect of ethyl acetate gum resin extract of B. serrata on hepatic function indicators
LPS resulted in a significant increase in the levels of ALT, AST, and ALP (P<0.001) and a considerable decline in serum concentration of albumin (P<0.05) and total protein (P<0.01). The levels of ALT, AST, and ALP were significantly decreased in groups treated with B. serrata extracts compared with the LPS group (P<0.01 and P<0.001). Moreover, B. serrata extract at 200 mg/kg increased the concentration of albumin (P<0.01) and total protein (P<0.001) [Figure 1] and [Figure 2].
|Figure 1: Serum level of alanine transaminase (ALT) (A), aspartate transaminase (AST) (B), and alkaline phosphatase (ALP) (C) in different groups. Data are indicated as mean ± SD (n= 8). ***P<0.001 versus the control group; ++P<0.01 and +++P<0.001 versus the LPS group. Ext 100 and 200: 100 and 200 mg/kg ethyl acetate gum resin extract of Boswellia serrata. LPS: lipopolysaccharide.|
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|Figure 2: Serum level of albumin (A), total protein (B), creatinine (C) and BUN (D) in different groups. Data are exhibited as mean ± SD (n= 8). *P<0.05, **P<0.01, ***P<0.001 versus the control group; +P<0.05, ++P<0.01 and +++P<0.001 versus the LPS group; $$P<0.01 versus the LPS-Ext 100. BUN: blood urea nitrogen.|
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3.2. Effect of ethyl acetate gum resin extract of B. serrata on kidney function indicators
The level of creatinine and BUN in LPS administered rats was increased compared with the control group (P<0.001). Pretreatment with 200 mg/kg of ethyl acetate gum resin extract of B. serrata significantly lowered the level of creatinine and BUN (P<0.05). However, there was no significant change in the level of creatinine and BUN in the group treated with 100 mg/kg of ethyl acetate gum resin extract of B. serrata compared with the LPS group [Figure 2]C and [Figure 2]D.
3.3. Effect of ethyl acetate gum resin extract of B. serrata on IL-6 in liver and kidney tissues
The level of IL-6 was increased in renal and hepatic tissues in LPS- treated rats (P<0.001) while it was noticeably diminished in LPS- exposed rats treated with 100 and 200 mg/kg of ethyl acetate gum resin extract of B. serrata (P<0.001). The IL-6 level in hepatic and renal tissues of the group treated with 200 mg/kg B. serrata extract was lower than that of the 100 mg/kg extract treated group (P<0.01 and P<0.001) [Figure 3]A and [Figure 3]B.
|Figure 3: Concentration of IL-6 in the hepatic (A) and renal (B) tissues of different groups. Data are shown as mean ± SD (n= 8). ***P< 0.001 versus the control group; +++P< 0.001 versus the LPS group; $$P<0.01 and $$$P<0.001 versus LPS-Ext 100.|
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3.4. Effect of ethyl acetate gum resin extract of B. serrata on oxidative stress indicators in kidney and liver tissues
Increased MDA level was observed in hepatic and renal tissues of the LPS group (P<0.001). Administration of 200 mg/kg of ethyl acetate gum resin extract of B. serrata lowered the MDA level in the hepatic tissue of LPS-administered rats (P<0.001). Moreover, the MDA level was reduced by treatment of 100 and 200 mg/kg of ethyl acetate gum resin extract of B. serrata in the renal tissue of LPS rats (P<0.001). The 200 mg/kg of ethyl acetate gum resin extract of B. serrata reduced MDA level in hepatic and renal tissues of the LPS group markedly compared with 100 mg/kg B. serrata extract (P<0.01) [Figure 4]A and [Figure 5]A.
|Figure 4: Effect of ethyl acetate gum resin extract of Boswellia serrata on oxidative stress indicators in the liver tissue of rats. (A) MDA, (B) the total thiol groups, (C) SOD, (D) CAT. Data are presented as mean ± SD (n= 8). ***P<0.001 versus the control group; +P<0.05, ++P<0.01 and +++P<0.001 versus the LPS group; $P<0.05, $$P<0.01 and $$$P<0.001 versus the LPS-Ext 100. MDA: malondialdehyde, SOD: superoxide dismutase, CAT: catalase.|
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|Figure 5: Effect of ethyl acetate gum resin extract of Boswellia serrata on oxidative stress indicators in the renal tissue of rats. (A) MDA, (B) the total thiol groups, (C) SOD, (D) CAT. Data are determined as mean ± SD (n= 8). ***P<0.001 versus the control group; +P<0.05 and +++P<0.001 versus the LPS group; $P<0.05 and $$P<0.01 versus LPS-Ext 100.|
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The concentration of total thiol groups in hepatic and renal tissues of the LPS group was lower than that of the control group (P<0.001). Both doses of ethyl acetate gum resin extract of B. serrata could reverse this change (P<0.05, P<0.01 and P<0.001). The total thiol content of hepatic (P<0.001) and renal (P<0.05) tissues in the 200 mg/kg B. serrata extract-treated group was higher than that of 100 mg/kg B. serrata extract-treated group [Figure 4]B and [Figure 5]B.
LPS injection also led to a noticeable decrease in SOD and CAT activities in hepatic and renal tissues (P<0.001). Administration of 100 and 200 mg/kg of ethyl acetate gum resin extract of B. serrata enhanced the activities of SOD and CAT in hepatic and renal tissues of rats (P<0.05 and P<0.001). Moreover, 200 mg/kg of ethyl acetate gum resin extract of B. serrata had more pronounced effects on increasing SOD and CAT activities (P<0.05, P<0.01) [Figure 4]C, [Figure 4]D, [Figure 5]C, and [Figure 5]D.
| 4. Discussion|| |
In this work, as a consequence of LPS-excited liver injury, the serum levels of ALT, AST, and ALP were increased and the concentrations of albumin and total protein were reduced. In addition, LPS-induced kidney dysfunction showed enhanced levels of creatinine and BUN. These pernicious effects of LPS can be referred to as the stimulation of inflammatory reactions and the induction of oxidative damage in hepatic and renal tissues as reported in previous studies,. In agreement with previous findings, a significant increment in the level of IL-6 and MDA and a noticeable decrement in total thiol groups concentration and SOD and CAT activities were found in hepatic and renal tissues of LPS- treated rats in the current research.
Pretreatment with ethyl acetate gum resin extract of B. serrata effectively ameliorated the impairment of liver and kidney function resulted from LPS administration. This finding is manifested by enhancement of albumin and total protein and reduction of liver enzymes, creatinine and BUN in rats treated by B. serrata extracts. Gum resin of B. serrata, known as frankincense, is used to alleviate various ailments excited by inflammation such as ulcerative colitis, rheumatoid arthritis, asthma, and osteoarthritis. Anti- inflammatory impacts of B. serrata are linked to the presence of constituents including O-acetyl-11-keto-β-boswellic acid (AKBA) and 11-keto-β-boswellic acid. AKBA has been identified to inhibit the NF-κB pathway and suppress the production of TNF-α, IL-1, and IL-6 from monocytes and macrophages. In addition, in ApoE-/- mice exposed to LPS, AKBA could downregulate inflammatory reactions via the inactivation of the NF-κB signaling pathway. Reduced secretion of IL-12 and interferon-γ (IFN-γ) and elevated release of IL-4 and IL-10 in monocytes treated with B. serrata extract have been also detected. In the current study, the ethyl acetate gum resin extract of B. serrata also modulated LPS- triggered inflammatory reactions in hepatic and renal tissues of rats, as evidenced by the decreased level of IL-6 in liver and kidney tissues of rats.
Alongside modulation of immune system activity, the role of B. serrata and its ingredients in the adjustment of oxidative status has been also understood. The end product of lipid production, MDA, is checked as a key oxidative stress indicator in experimental works. Boswellic acid from the gum resin of B. serrata has been found to reduce brain oxidative injury and ameliorate memory by lowering the MDA level and raising the glutathione concentration in rats challenged by trimethyltin. Modification of lipid peroxidation followed by monosodium-urate crystals-induced inflammation has been also attributed to boswellic acid. In an experimental study, the administration of oleo gum resin of B. serrata could improve the decreased activity of CAT resulted from CCL4 in hepatic tissue. Decline in MDA concentration and elevation of total thiol content and CAT and SOD activities were also observed in the present study in groups treated with ethyl acetate gum resin extract of B. serrata compared with the LPS group. Therefore, the inhibition of inflammatory reactions and modulation of oxidative stress by ethyl acetate gum resin extract of B. serrata may be contributed to alleviation of LPS-induced hepatic and renal damages. However, in terms of the effect of the B. serrata extract on improvement of LPS- induced inflammation and oxidative damage in the liver and kidney, 200 mg/kg of extract had a better effect than 100 mg/kg of extract. This finding was supported by a more markedly decreased level of IL-6 and MDA and increased concentration of total thiol and SOD and CAT activity in the group treated with 200 mg/kg of extract.
In conclusion, the ethyl acetate gum resin extract of B. serrata alleviated LPS-induced inflammation and oxidative stress in the liver and kidney. However, the assessment of molecular and pathological indicators can be useful to determine more precise mechanism(s) of the effect of ethyl acetate gum resin extract of B. serrata on LPS-induced liver and kidney malfunction, which needs further investigation in the future.
Conflict of interest statement
The authors declare that there is no conflict of interest.
The authors would like to thank the Vice Presidency of Research of Jiroft University of Medical Sciences for their support.
NM, FB and PE performed experiments and collected data. AA and MH analyzed data. AA prepared manuscript and MH revised it.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]