|Year : 2021 | Volume
| Issue : 11 | Page : 491-499
Anti-inflammatory and antipyretic potential of Arbutus andrachne L. methanolic leaf extract in rats
Sahar M Jaffal1, Sawsan A Oran1, Mohammad I Alsalem2
1 Department of Biological Sciences, Faculty of Science, The University of Jordan, 11942 Amman, Jordan
2 Department of Anatomy and Histology, Faculty of Medicine, The University of Jordan, 11942 Amman, Jordan
|Date of Submission||09-Jun-2021|
|Date of Decision||01-Jul-2021|
|Date of Acceptance||02-Sep-2021|
|Date of Web Publication||29-Oct-2021|
Sahar M Jaffal
Department of Biological Sciences, Faculty of Science, The University of Jordan, 11942 Amman
Source of Support: This project was funded by the Deanship of Scientific Research, The University of Jordan (235/2020/19), Conflict of Interest: None
Objective: To explore the anti-inflammatory and antipyretic effects of methanolic leaf extract from Arbutus andrachne and its mechanism of action.
Methods: Paw edema was induced by intraplantar (i.pl.) injection of λ-carrageenan (1% w/v, 100 μL/paw) while pyrexia was evoked by intraperitoneal (i.p.) injection of 20% baker’s yeast (20 mL/kg body wt) in male Wistar rats. The anti-inflammatory and antipyretic effects of Arbutus andrachne methanolic leaf extract were explored by injecting rats with different doses of the plant extract (150, 300, and 600 mg/kg body wt, i.p.). Selective antagonists for transient receptor potential vanilloid-1 (TRPV1), cannabinoid receptor 1 (CB1), and alpha-2 adrenergic receptor (a2-AR) were used to unravel the extracts’ mechanism of action. Blood samples were collected from the heart of rats to measure the levels of interleukin-6 (IL-6) and prostaglandin E2 (PGE2) by enzyme-linked immunosorbent assay.
Results: The extract exhibited potent anti-inflammatory activity by decreasing paw thickness and IL-6 levels. In addition, yeast-evoked pyrexia was attenuated by the extract treatment via TRPV1 and CB1 receptors and a reduction in PGE2 levels. No significant effects were found for a2-AR. Moreover, the rats that received the plant extract demonstrated similar responses to the positive control group.
Conclusions: Arbutus andrachne can be a good candidate for treating inflammation and pyrexia and should be further investigated.
Keywords: Arbutus andrachne; Anti-inflammatory; Antipyretic; PGE2; IL-6; TRPV1; CB1; a2-ARs
|How to cite this article:|
Jaffal SM, Oran SA, Alsalem MI. Anti-inflammatory and antipyretic potential of Arbutus andrachne L. methanolic leaf extract in rats. Asian Pac J Trop Biomed 2021;11:491-9
|How to cite this URL:|
Jaffal SM, Oran SA, Alsalem MI. Anti-inflammatory and antipyretic potential of Arbutus andrachne L. methanolic leaf extract in rats. Asian Pac J Trop Biomed [serial online] 2021 [cited 2021 Nov 26];11:491-9. Available from: https://www.apjtb.org/text.asp?2021/11/11/491/328056
| 1. Introduction|| |
Inflammation is a natural biological process that occurs in response to harmful stimuli. During inflammation, several inflammatory mediators are released at the injured tissue to induce vasodilation in addition to leakage of plasma, fluids, and white blood cells into the site of inflammation to start tissue repair. Pyrexia (fever) is another normal response initiated in the body to fight infection. It is a complex process described as a rise in body temperature triggered by exogenous or endogenous stimuli known as pyrogens. Notably, some common mediators take part in the development of inflammation and fever such as prostaglandin E2 (PGE2) and interleukin-6 (IL-6). PGE2 increases vascular permeability and strengthens the role of other inflammatory mediators. Also, PGE2 contributes to the increase in body temperature by acting on the thermoregulatory center in the hypothalamus. Besides, IL-6 is a multifunctional cytokine that evokes the production of many proteins responsible for inflammatory reactions. Different types of cells (e.g. fibroblasts, endothelial and epithelial cells) produce IL-6. Importantly, IL-6 is a vital mediator in the transition from acute to chronic phase of inflammation. It issues a warning signal in case of environmental stress conditions (e.g. tissue damage or infection) leading to the activation of defense mechanisms. Unfortunately, currently used anti-inflammatory and antipyretic drugs have undesirable effects urging the need to find new anti-inflammatory and antipyretic candidates. In this regard, medicinal plants are rich sources for compounds that have promising therapeutic values with a wide margin of safety. In Jordan, there are 363 medicinal plants including Arbutus andrachne (A. andrachne) L. (Ericaceae) which is a flowering tree that grows in Jordan in the regions of Jarash, Ajloun, Irbid, Salt, and Amman. The plant is used as an edible plant, in traditional medicine as well as stain industry. In particular, the leaves and fruits of A. andrachne are consumed as laxatives, blood tonic, diuretics, and antiseptics. Several biological studies were conducted to explore the effects of A. andrachne in different models. Most importantly, A. andrachne extract showed strong anti-nociceptive activity. In addition, 17 active compounds were identified in A. andrachne methanolic leaf extract by liquid chromatography mass spectrometry (LC-MS). The compounds include linalool, lauric acid, myristic acid, linoleic acid, rutin, arbutin, hydroquinone, β-sitosterol, ursolic acid, isoquercitrin, myricetin-3-O-a-L-rhamnosides, quercetin, gallic acid, (+)-gallocatechin, kaempferol, catechin gallate, and a-tocopherol.
Although many reports were published about the biological activities of A. andrachne, to the best of our knowledge, none of the previous studies explored the in vivo anti-inflammatory and antipyretic effects of A. andrachne and its mechanism of action. In the present study, we examined the roles of A. andrachne methanolic leaf extract on carrageenan-induced paw edema and yeast-evoked pyrexia models as well as the mechanisms of action that underlie these effects. We focused on investigating the role of the transient receptor potential vanilloid-1 (TRPV1), cannabinoid receptor 1 (CB1), and alpha-2 adrenergic receptor (a2-AR) in the anti-inflammatory and antipyretic activities of A. andrachne. TRPV1 is a non-selective cation channel that is involved in many processes including thermoregulation, different painful and inflammatory conditions,. Due to the diverse roles of TRPV1, many disorders and diseases were associated with alterations in the expression and/ or function of TRPV1 such as asthma, inflammation, and itch,. Furthermore, CB1 receptor is one of the CB receptors that take part in inflammation and pyrexia. Importantly, it was reported that the endocannabinoid arachidonoylethanolamine enhances lipopolysaccharide (LPS)-induced fever by the activation of CB1 receptor. Also, Alsalem et al. pointed out that the intra-articular injection of synthetic cannabinoids and palmitoylethanolamide to a rat model of arthritis restored paw withdrawal threshold and weight-bearing differences. Furthermore, the peripheral administration of anandamide inhibited thermal hyperalgesia through CB1 receptor in a carrageenan-induced edema model in rats. With respect to the noradrenergic system, it is well recognized that noradrenergic receptors play pivotal roles in pain and inflammation and are considered targets for inflammatory and neuropathic pain treatment. It was reported that the intrathecal application of α2-AR agonist clonidine alleviated complete Freund’s adjuvant-induced pain and produced changes in several signaling molecules.
| 2. Materials and methods|| |
SR141716A, capsazepine, and yohimbine were purchased from Tocris Bioscience, Bristol, UK. Diclofenac sodium was brought from Novartis, Basel, Switzerland. Lambda (λ)-carrageenan was ordered from Santa-Cruz Biotechnology, Dallas, USA. Commercially available dried baker’s yeast (Saccharomyces cerevisiae) was purchased from the market, Amman, Jordan. PGE2 kit was supplied by Abcam, Cambridge, UK while IL-6 kit was from RayBiotech, Norcross, USA. Diethyl ether was purchased from Scharlau, Barcelona, Spain. Sterile normal saline was from McKesson, Virginia, USA.
2.2. Preparation of drugs
The stocks of antagonists (except yohimbine) were initially dissolved in absolute ethanol (10 mM capsazepine, 1 mM SR141716A). All drugs were freshly prepared (from stock) before use and were diluted in sterile saline. Yohimbine and diclofenac sodium were directly dissolved in saline. Hot saline (80 °C) was used to dissolve λ-carrageenan while warm saline (40 °C) was used to dissolve the baker’s yeast.
2.3. Collection of the plant leaves
The leaves of A. andrachne were gathered from Jarash, Jordan in March 2019. The plant was authentically identified by a plant taxonomist (Prof. Sawsan Oran) in the Department of Biological Sciences, the University of Jordan. A voucher specimen (UJ/05/2020) was placed at the herbarium, Department of Biological Sciences, the University of Jordan.
2.4. Preparing the methanolic extract from A. andrachne leaves
The leaves of A. andrachne were washed, dried, and ground with a blender. Methanol (10:1 v/w ratio) was used to soak the dried leaves with shaking at room temperature for 3 d. The extract was filtered by Whatman filter paper followed by evaporating the solution in a rotary evaporator maintained at 45 °C under reduced pressure. The procedure was repeated several times. The extract was weighed to calculate the yield percentage using the following equation: Yield % = (weight of dry extract/weight of dry leaves before extraction) × 100%. The extract was kept in an air tight container in the freezer.
Male Wistar rats (200-250 g) were used in the experiment of carrageenan-induced edema (n=54) while rats weighing 70-100 g were used in the experiment of yeast-induced pyrexia (n=54). All animals were brought from the animal house, the University of Jordan and were kept at the same unit in a temperature-controlled environment [(22 ± 1) °C] with a cycle of 12 h lightness and 12 h darkness. Food pellets and water were provided ad libitum. The animals were allowed to adapt to the experimental room’s conditions before conducting the tests.
2.6. Carrageenan-induced paw edema
The anti-inflammatory effect of A. andrachne extract was examined using a carrageenan-induced paw edema model in rats. Paw size was determined before and after carrageenan injection by wrapping a thread around the paw of rats and measuring the thread’s length (paw circumference) using a metric ruler. The animals were divided into control and experimental groups. Different groups received vehicle or plant extract (150, 300, and 600 mg/kg body wt) intraperitoneally (i.p.) while the positive control group received diclofenac sodium (30 mg/kg body wt, i.p.) 30 min before intraplantar (i.pl.) injection of 1% w/v freshly prepared λ-carrageenan (100 μL/paw) into the left hind paw. The injection of carrageenan was performed under 2% diethyl ether anesthesia. Different antagonists were used to explore the extract’s mechanism of action in inducing its anti-inflammatory effect as the following: 0.1 mg/kg body wt capsazepine (a selective TRPV1 antagonist), 0.1 mg/kg body wt SR141716A (a selective CB1 antagonist), and 1 mg/kg body wt yohimbine (a selective antagonist for a2-AR). The antagonists were i.p. administered 30 min before the chosen dose of A. andrachne extract (300 mg/kg body wt). The behavior of animals was noticed and recorded in all treated groups. Paw size was measured in all animals after 1, 2, 3, and 4 h of carrageenan injection. Images for paws’ plantar surface of different rats were captured before and after treatment using a digital compact camera (Canon, Melville, USA). The percentage of edema was calculated using the following equation: [(Cac-C0)/C0] ×100% where Cac is the paw thickness after carrageenan injection, C0 is the paw thickness before carrageenan injection (baseline). The animals were sacrificed after 5 h of carrageenan injection to collect blood samples from the heart of rats. The blood was kept for 30 min at room temperature to allow blood coagulation and separate the serum. Samples were then centrifuged at 1 300 ×g for 15 min. The supernatant was preserved at –20 °C before use for determining the levels of IL-6 by enzyme-linked immunosorbent assay (ELISA).
2.7. Determination of IL-6 levels in serum samples
All reagents and IL-6 standards (0-10 000 pg/mL) were prepared as explained by the manufacturer. The standards or samples (100 μL) were added to each well and incubated at room temperature with gentle shaking for 2.5 h. The wells were washed with 1× wash buffer 4 times. The remaining wash solution was removed by blotting the plate against paper towels. After that, 100 μL of 1× biotinylated antibody was added and incubated with shaking for 1 h at room temperature followed by 4 times wash as in the previous step. The next step included the addition of 100 μL streptavidin, and 45 min incubation at room temperature with gentle shaking followed by 4 times wash. Subsequently, 100 μL of 3,3’, 5, 5’-tetramethylbenzidine substrate was added and incubated for 30 min in the dark at room temperature. Finally, 50 μL stop solution was added to yield a yellow colour that can be photometrically measured at 450 nm. The added volumes that were mentioned in this section represent the volumes per every well. Calculations of IL-6 levels in different samples were performed based on the standard curve.
2.8. Yeast-induced pyrexia
To evaluate the effect of the plant extract on yeast-evoked pyrexia, the experiment was conducted in a temperature-controlled environment [(22 ± 1) °C]. Digital thermometer was used to determine the body temperature of each rat before and after treatments. The thermometer was inserted into the rectum for 45 s. Pyrexia was induced by i.p. injection of 20% baker’s yeast dissolved in normal saline (20 mL/kg body wt). Following yeast injection, the animals were kept to fast for 6 h with water provided ad libitum. After 6 h, body temperature was measured to select the animals that had a rise between 0.5-1 °C and then they were divided into different groups. After that, the animals received i.p. injection of different treatments including various doses of the plant extract (150, 300, and 600 mg/kg body wt), vehicle, or diclofenac sodium. Different antagonists were used in this part of the experiment as the following: 0.1 mg/kg body wt capsazepine, 0.1 mg/kg body wt SR141716A and 1 mg/kg body wt yohimbine. The antagonists were i.p. administered 30 min before A. andrachne extract (300 mg/kg body wt). In all groups, body temperature was measured every 1 h. The percent change in yeast-evoked body temperature was calculated using the following equation: (TAT–TAP)/(TAP–Tb)×100% where TAT is the temperature measured after treatments, TAP is the temperature measured post yeast injection (after pyrexia), and Tb is the baseline temperature, measured before yeast injection. After 5 h of the final treatment, the animals were euthanized to collect blood samples from the heart. The blood samples were kept to coagulate for 30 min at room temperature and were centrifuged at 1 300 ×g, 4 °C for 15 min. The supernatant was preserved at –20 °C to determine PGE2 levels.
2.9. Determination of PGE2 levels in serum samples
PGE2 levels in different serum samples were determined using ELISA kit. All reagents were prepared according to the manufacturer’s instruction. Briefly, the standards, samples, or diluent solutions were prepared and added to the 96-well plate provided in the kit. After the addition of PGE2 and alkaline phosphatase, the standards and samples were exposed to PGE2 antibody with shaking at room temperature for 2 h followed by 3 times wash. The excess wash buffer was removed by tapping the 96-well plate onto paper towels followed by the addition of the p-nitrophenyl phosphatesubstrate and stop solution. Afterwards, the optical density was measured at 405 nm with correction at 590 nm pursuant to the manufacturer’s instructions. Calculations of PGE2 levels in different samples were performed based on the standard curve.
2.10. Open field test
The locomoter activity of all animals was examined by the open field test using Opto-M4, Columbus instrument. The instrument contains dual horizontal planes with infrared beams placed on the top of the cage. On the bottom of the cage, there are detectors that detect beams’ interruption by the movement of the animal crossing the infrared beam. The number of beam interruptions was summed every 5-20 min by the instrument software and was sent to a computer being connected to the machine. The results were displayed on the software and exported to excel file.
2.11. Statistical analysis
Data were presented as mean ± standard error of means (SEM). The normality test was conducted for all groups using Shapiro-Wilk test. The statistical significance of difference between groups was assessed by one-way analysis of variance (ANOVA) followed by the suitable post-hoc test (Tukey’s test). P<0.05 was considered significant. GraphPad Prism version 7 was used to create figures and perform the statistical analysis.
2.12. Ethical statement
All experiments were approved by the Animal Ethics Committee at the University of Jordan (Ethical approval number 235/2020/19).
| 3. Results|| |
3.1. Yield of A. andrachne methanolic leaf extract
Using the extraction method described in the methodology section, 5 g of powder leaves (soaked in 50 mL methanol) produced 1.5 g extract (15% yield). The extract was used for screening its biological activities in animals.
3.2. Effect of A. andrachne leaf extract on carrageenan-induced inflammation
In this study, inflammation was induced by i.pl. injection of λ-carrageenan (1% w/v) into the hind paw of rats whereby the increase in footpad thickness was considered edema. The i.pl. injection of 1% carrageenan into the left hind paw of animals significantly increased footpad thickness by (45.96 ± 4.79)%, (61.44 ± 4.19)%, (63.97 ± 5.22)% and (75.10 ± 4.95)% after 1, 2, 3 and 4 h of injection, respectively. At 1-hour post carrageenan injection, the percentage of paw edema was lower in the groups that received different treatments: 150 mg/kg body wt (5.27 ± 1.00)%, 300 mg/kg body wt (4.02 ± 1.00)%, and 600 mg/kg body wt A. andrachne extract (4.90 ± 1.49)% as well as 30 mg/kg body wt diclofenac sodium (7.38 ± 1.45)% [Figure 1]A. After 2 h of carrageenan injection, the percentage of paw swelling reached (10.55 ± 3.40)%, (10.15 ± 2.68)%, (11.35 ± 1.83)% and (11.78 ± 5.10)% in the groups that received 150, 300, and 600 mg/ kg body wt A. andrachne as well as 30 mg/kg body wt diclofenac sodium, respectively [Figure 1]B. In the third and fourth hour after carrageenan injection, the groups that were treated with 150, 300, 600 mg/kg body wt A. andrachne extract and 30 mg/kg body wt diclofenac sodium still exhibited markedly lower percentage of paw edema compared with the carrageenan group [Figure 1]C and [Figure 1]D. Clearly, inflammation subsided in the groups that received the plant extract before carrageenan injection. Notably, paw thickness in A. andrachne-treated groups was comparable to the thickness in the group that received the standard drug diclofenac sodium at all measured time points. [Figure 2] displays representative photographs (at selected time points) for the paw thickness of rats. Based on the aforementioned results, the most effective dose of A. andrachne leaf extract (300 mg/kg body wt) was chosen to examine the impact of different antagonists on the anti-inflammatory effect exhibited by the extract. None of the antagonists used in this study abolished or decreased the noticeable activity of the extract on carrageenan-induced edema at any time point [Figure 1]A,[Figure 1]B,[Figure 1]C,[Figure 1]D. Moreover, the i.pl. injection of carrageenan increased IL-6 levels significantly compared with the control group while A. andrachne leaf extract (150, 300, and 600 mg/kg body wt) attenuated IL-6 levels compared with the carrageenan-treated group [Figure 3]. Notably, only TRPV1 and CB1 antagonists abolished the effect of 300 mg/kg body wt A. andrachne on IL-6 levels in the carrageenan-induced paw edema model. It was also noted that there were no toxic signs in the skin, eyes, behaviour (salivation, lethargy, and sleepiness), urination, diarrhea, or mortality in any of the groups that received different doses of A. andrachne extract used in this study. Moreover, the i.p. injection of the methanolic leaf extract did not affect the locomotor activity of animals when tested in the open field test (data not shown) ruling out the possibility that there was sedative effect or impairment in animal locomotion.
|Figure 1: Percentage of paw edema in rats receiving different treatments after 1 (A), 2 (B), 3 (C) and 4 (D) h of carrageenan injection. The data are presented as mean±SEM (n=6), and analyzed by one-way ANOVA followed by Tukey’s test. *Significant difference vs. the control group, P<0.001. #Significant difference vs. the carrageenan-treated group, P<0.001.|
Click here to view
|Figure 2: Photographs showing paw sizes over time in different treatment groups.|
Click here to view
|Figure 3: IL-6 levels in different treatment groups. The data are presented as mean±SEM (n=6), and analyzed by one-way ANOVA followed by Tukey’s test. *Significant difference compared with the control group, P<0.001. #Significant difference compared with the carrageenan-treated group, P<0.001. **Significant difference compared with the 300 mg/kg body wt A. andrachne treated group, P<0.001.|
Click here to view
3.3. Effect of A. andrachne leaf extract on yeast-evoked pyrexia
A yeast-evoked pyrexia model was employed to screen the antipyretic effect of the plant extract and the role of different receptors in mediating its activity. The i.p. injection of 20% yeast suspension (20 mL/kg) had a robust effect on body temperature of animals and induced fever after 6 h of injection. Yeast injection increased body temperature by (17.51 ± 9.20)%, (53.90 ± 13.71)%, (55.76 ± 9.50)% and (49.75 ± 2.10)% after 1, 2, 3 and 4 h, respectively. Similar to the activity of diclofenac sodium, the i.p. injection of A. andrachne extract decreased yeast-induced elevation in body temperature after 1, 2, 3, and 4 h of injection [Figure 4]A,[Figure 4]B,[Figure 4]C,[Figure 4]D. The maximum antipyretic effect was noticed in the group that received 300 mg/kg body wt A. andrachne extract. Accordingly, this dose was selected to assess the involvement of certain receptors in the animals’ response to the plant extract. Of the antagonists administered before 300 mg/kg body wt A. andrachne, only TRPV1 and CB1 antagonists reversed the effect of the plant extract in reducing pyrexia at all measured time points [Figure 4]A,[Figure 4]B,[Figure 4]C,[Figure 4]D. As expected, the administration of yeast increased PGE2 levels significantly (4 164 ± 277) pg/mL compared with the control group (1 910.00 ± 25.43) pg/mL. Interestingly, there was a dramatic decrease in PGE2 levels [(2 893 ± 285) pg/mL] in the group that received 300 mg/kg body wt A. andrachne leaf extract compared with carrageenan-treated group [Figure 5]. This decrease was not abrogated by pre-injecting the animals with TRPV1, CB1, or a2-AR antagonists.
|Figure 4: Percent change in rectal body temperature in different groups after 1 (A), 2 (B), 3 (C) and 4 (D) h of A. andrachne extract treatment. The data are presented as mean±SEM (n=6), and analyzed by one-way ANOVA followed by Tukey’s test. #Significant difference compared with the yeast-treated group, P<0.001. **Significant difference compared with the 300 mg/kg body wt A. andrachne and yeast-treated group, P<0.001.|
Click here to view
|Figure 5: PGE2 levels in different tretament groups. The data are presented as mean±SEM (n=6), and analyzed by one-way ANOVA followed by Tukey’s test. *Significant difference compared with the control group, P<0.001. #Significant difference compared with the yeast-treated group, P<0.001.|
Click here to view
| 4. Discussion|| |
There is an urgent need for new powerful anti-inflammatory and antipyretic drugs that have a good margin of safety. Medicinal plants are considered promising sources for therapeutic compounds and can be valuable candidates. A large number of researches showed that A. andrachne had several biological activities. However, to the best of our knowledge, none of the previous studies determined the anti-nociceptive, in vivo anti-inflammatory and antipyretic effects of A. andrachne. Previously, we showed that A. andrachne exhibited anti-nociceptive effect in different models. The current study put the light on new valuable effects of A. andrachne leaf extract that was yet to be determined in previous studies. It proves potent anti-inflammatory and antipyretic potential of A. andrachne extract and validates its mechanism of action. In more detail, all doses of A. andrachne extract significantly decreased carrageenan-induced swelling in animal footpads indicating that A. andrachne is a regulator for inflammation. The effect was accompanied by a decrease in IL-6 levels. Interestingly, 17 compounds were identified in A. andrachne methanolic leaf extract by LC-MS. These compounds have effects on inflammation and IL-6 levels as documented in earlier reports. Peana and co-workers reported the anti-inflammatory role of linalool in carrageenan-induced paw edema model after 1, 3, and 5 h of injection. Moreover, Liu et al. found that treating neutrophils with 40 μM quercetin before LPS administration decreased the expression of IL-6 mRNA, intracellular IL-6, and IL-6 secretion. Similarly, IL-6 suppression was reported by treatment with isoquercetin, β-sitosterol, and ursolic acid in different models,,. Moreover, it was shown that a-tocopherol exhibited anti-inflammatory activities in human and animal studies. The administration of a-tocopherol to the animals 3 d before LPS treatment attenuated IL-6 levels in cardiac and skeletal muscles. Besides, Marion-Letellier and colleagues showed that linoleic acid diminished the secretion of pro-inflammatory cytokines such as IL-6. Likewise, it was noted that lauric acid demonstrated anti-inflammatory activity in rats whereby rutin decreased ankylosis, edema, and nodules,. Also, arbutin exhibited anti-inflammatory properties in LPS-induced microglial cells and decreased IL-6 levels while β-sitosterol had anti-inflammatory activities in different models of paw edema induced by 12-O-tetradecanoylphorbol acetate, arachidonic acid, and carrageenan in rodents. Similarly, myricetin displayed anti-inflammatory roles in multiple models including rheumatoid arthritis, carrageenan-induced inflammation, xylene-induced ear edema, and periodontitis infectious inflammatory disease. Besides, much attention was paid to the broad spectrum of anti-inflammatory activities exhibited by kaempferol. Kroes et al. pointed out that gallic acid demonstrated an anti-inflammatory effect against zymosan-induced footpad swelling in mice. It was also noted that epigallocatechin-3-gallate inhibited the synthesis of IL-6 in adjuvant-induced arthritis rat model. With respect to the antipyretic effect exhibited by the plant extract, the effect can be also ascribed to many active compounds of the plant that had antipyretic activities as reported in the literature. The reversal of yeast-evoked pyrexia was demonstrated after the use of virgin coconut oil that contains lauric, myristic, and linoleic acids as active ingredients. Additionally, Fawad et al. reported that 2 derivatives of hydroquinone significantly reduced the febrile response in rats. Linalool, rutin, ursolic acid, β-sitosterol, isoquercetin, quercetin, gallocatechin, kaempferol, and gallic acid were also compounds identified in many plant extracts that demonstrated potent antipyretic effects in previous studies,,,,. Importantly, the antipyretic effect of A. andrachne extract shown in the current study was accompanied by a decrease in PGE2 levels. In this regard, previous studies revealed that several flavonoids (e.g. quercetin and kaempferol) prevented LPS-induced PGE2 production. Similar findings were reported for the effect of other compounds including isoquercetin, rutin, and myricetin on LPS-induced PGE2 production in macrophages. Likewise, treating macrophages with a-tocopherol decreased PGE2 levels while the administration of epigallocatechin-3-gallate attenuated the levels of PGE2 induced by photofrin mediated photodynamic therapy. Of note, earlier reports showed the involvement of TRPV1 and/or CB1 receptor in the anti-nociception effects induced by the active constituents of A. andrachne extract. These reports are listed in detail in Jaffal et al.. It merits explaining the involvement of TRPV1 and CB1 antagonists in reversing the effect of A. andrachne extract on serum IL-6 levels of the animals in carrageenan-induced paw edema despite not being implicated in the anti-inflammatory activity of the extract. Another fact that needs explanation is that the antagonists of the TRPV1 and CB1 receptors were implicated in abolishing the antipyretic effect of the extract but not PGE2 levels in serum samples that were taken from the animals in this model. In this regard, we previously found that the anti-nociceptive effect of the plant extract was mediated by several receptors including TRPV1, CB1, peroxisome proliferator-activated receptor a and gamma (γ). These receptors were differentially implicated in hot plate test, tail flick test and formalin-induced paw licking test. Therefore, we expect that other receptors are involved in A. andrachne-induced anti-inflammatory action or in the decrease of PGE2 levels evoked by A. andrachne extract in yeast-induced pyrexia model whereby TRPV1 and CB1 receptors were not involved. Further work is needed to investigate the involvement of other receptors in these activities of the leaf extract.
Notably, the present study had some limitations. Other inflammatory mediators should be determined to further confirm the effect of the A. andrachne extract and different models should be established to further evaluate the anti-inflammatory effects of the extract.
Taken together, the data of the current research proved potent anti-inflammatory and antipyretic effects of A. andrachne leaf extract with a decrease in the levels of IL-6 and PGE2. A. andrachne can be a good candidate for development of new anti-inflammatory and antipyretic agents with fewer side effects.
Conflict of interest statement
The authors have no conflict of interest.
The authors acknowledge the Deanship of Scientific Research, The University of Jordan.
This project was funded by the Deanship of Scientific Research, The University of Jordan (235/2020/19).
SMJ designed the experiments, collected, analyzed and interpreted the data, and drafted the article. SAO collected and identified the plant and supervised the project. MIA designed the experiments, supervised the project, and critically read the article. All authors approved the final version of the published manuscript.
| References|| |
gEze FI, Uzor PF, Ikechukwu P, Obi BC, Osadebe PO. In vitro
and in vivo
models for anti-inflammation: An evaluative review. ITPS
Blomqvist A, Engblom D. Neural mechanisms of inflammation-induced fever. Neuroscientist
Newton RF, Roberts SM. Prostaglandins and thromboxanes: Butterworths monographs in chemistry
. 1st ed. London: Butterworth-Heinemann; 2016.
Prajitha N, Athira SS, Mohanan PV. Pyrogens, a polypeptide produces fever by metabolic changes in hypothalamus: Mechanisms and detections. Immunol Lett
Tsuge K, Inazumi T, Shimamoto A, Sugimoto Y. Molecular mechanisms underlying prostaglandin E2
-exacerbated inflammation and immune diseases. Int Immunol
Kaur S, Bansal Y, Kumar R, Bansal G. A panoramic review of IL-6: Structure, pathophysiological roles and inhibitors. Bioorg Med Chem
Dar RA, Shahnawaz M, Qazi PH. General overview of medicinal plants: A review. J Phytopharm
Oran SA. The status of medicinal plants in Jordan. JAST
Oran SA. Selected wild aromatic plants in Jordan. Int J Med Plants (Photon)
Jaffal SM, OranSA, Alsalem M. Anti-nociceptive effect of Arbutus andrachne
methanolic leaf extract mediated by CB1, TRPV1 and PPARs in mouse pain models. Inflammopharmacology
Caterina MJ, Schumacher MA, Tominaga M, Rosen TA, Levine JD, Julius D. The capsaicin receptor a heat-activated ion channel in the pain pathway. Nature
Alsalem M, Wong A, Millns P, Arya PH, Chan MSL, Bennett A, et al. The contribution of the endogenous TRPV1 ligands 9-HODE and 13-HODE to nociceptive processing and their role in peripheral inflammatory pain mechanisms. Br J Pharmacol
El-Hashim AZ, Jaffal SM. Nerve growth factor enhances cough and airway obstruction via
TrkA receptor- and TRPV1-dependent mechanisms. Thorax
Feng J,Yang P, Mack MR, Dryn D, Luo J, Gong X, et al. Sensory TRP channels contribute differentially to skin inflammation and persistent itch. Nat Commun
Fraga D, Zanoni CIS, Rae GA, Parada CA, Souza GEP. Endogenous cannabinoids induce fever through the activation of CB1 receptors. Br J Pharmacol
Alsalem M, Haddad M, Aldossary SA, Kalbouneh H, Altarifi A, Jaffal SM, et al. Role of cannabinoid receptor 1 and the peroxisome proliferator-activated receptor a in mediating anti-nociceptive effects of synthetic cannabinoids and a cannabinoid-like compound. Inflammopharmacology
Bouchet CA, Ingram SL. Cannabinoids in the descending pain modulatory circuit: Role in inflammation. Pharmacol Ther
Carbone E. Noradrenergic inhibition of presynaptic TRPV1 channels: A new pathway of pain control. J Physiol
Peana AT, D’Aquila PS, Panin F, Serra G, Pippia P, Moretti MDL. Anti-inflammatory activity of linalool and linalyl acetate constituents of essential oils. Phytomedicine
Liu JJ, Song CW, Yue Y, Duan CG, Yang J, He T, et al. Quercetin inhibits LPS-induced delay in spontaneous apoptosis and activation of neutrophils. Inflamm Res
Checker R, Sandur SK, Sharma D, Patwardhan RS, Jayakumar S, Kohli V, et al. Potent anti-inflammatory activity of ursolic acid, a triterpenoid antioxidant, is mediated through suppression of NF-κB, AP-1 and NF-AT. PLoS One
Li L, Zhang XH, Liu GR, Liu C, Dong YM. Isoquercitrin suppresses the expression of histamine and pro-inflammatory cytokines by inhibiting the activation of MAP kinases and NF-κB in human KU812 cells. Chin J Nat Med
Sun Y, Gao L, Hou W, Wu J. β-Sitosterol alleviates inflammatory response via
inhibiting the activation of ERK/p38 and NF-κB pathways in LPS-exposed BV2 cells. Biomed Res Int
Reiter E, Jiang Q, Christen S. Anti-inflammatory properties of a- and γ-tocopherol. Mol Asp Med
Huey KA, Fiscus G, Richwine AF, Johnson RW, Meador BM. In vivo
vitamin E administration attenuates interleukin-6 and interleukin-1β responses to an acute inflammatory insult in mouse skeletal and cardiac muscle. Exp Physiol
Marion-Letellier R, Butler M, Déchelotte P, Playford RJ, Ghosh S. Comparison of cytokine modulation by natural peroxisome proliferator–activated receptor γ ligands with synthetic ligands in intestinal-like Caco-2 cells and human dendritic cells—potential for dietary modulation of peroxisome proliferator–activated receptor γ in intestinal inflammation. Am J Clinl Nutr
Sekar S, Panchal SK, Ghattamaneni NKR, Brown L, Crawford R, Xiao Y, et al. Dietary saturated fatty acids modulate pain behaviour in trauma-induced osteoarthritis in rats. Nutrients
Guardia T, Rotelli AE, Juarez AO, Pelzer LE. Anti-inflammatory properties of plant flavonoids. Effects of rutin quercetin and hesperidin on adjuvant arthritis in rat. Farmaco
Lee HJ, Kim KW. Anti-inflammatory effects of arbutin in lipopolysaccharide-stimulated BV2 microglial cells. Inflamm Res
Nirmal SA, Pal SC, Mandal SC, Patil AN. Analgesic and anti-inflammatory activity of β-sitosterol isolated from Nyctanthes arbortristis
Semwal D, Semwal R, Combrinck S, Viljoen A. Myricetin: A dietary molecule with diverse biological activities. Nutrients
Devi KP, Malar DS, Nabavi SF, Sureda A, Xiao J, Nabavi SM, et al. Kaempferol and inflammation: From chemistry to medicine. Pharmacol Res
Kroes B, van den Berg A, Quarles van Ufford H, van Dijk H, Labadie R. Anti-inflammatory activity of gallic acid. Planta Med
Ahmed S, Marotte H, Kwan K, Ruth JH, Campbell PL, Rabquer BJ, et al. Epigallocatechin-3-gallate inhibits IL-6 synthesis and suppresses trans-signaling by enhancing soluble gp130 production. Proc Natl Acad Sci U S A
Intahphuak S, Khonsung P, Panthong A. Anti-inflammatory analgesic and antipyretic activities of virgin coconut oil. Pharm Biol
Fawad K, Ul-Islam N, Subhan F, Shahid M, Ali G, Rahman FU, et al. Novel hydroquinone derivatives alleviate algesia inflammation and pyrexia in the absence of gastric ulcerogenicity. Trop J Pharm Res
Zhou B, Tan M, Lu J, Zhao J, Xie A, Li S. Simultaneous determination of five active compounds in Chimonanthus nitens
by double-development HPTLC and scanning densitometry. Chem Cent J
Afsar T, Khan MR, Razak S, Ullah S, Mirza B. Antipyretic anti-inflammatory and analgesic activity of Acacia hydaspica
R. Parker and its phytochemical analysis. BMC Complem Altern Med
Dwivedi J, Gupta A, Verma S, Paliwal S, Rawat AKS. Validated simultaneous high-performance thin-layer chromatographic analysis of ursolic acid, β-sitosterol, lupeol and quercetin in the methanolic fraction of Ichnocarpus frutescens. JPC
Vasudevan CN, Kariyil BJ, Nair DA, Neerakkal I. Screening of phytocompounds, molecular docking studies, and in vivo
anti-inflammatory activity of heartwood aqueous extract of Pterocarpus santalinus
L.f. Asian Pac J Trop Biomed
Ullah I, Khan JA, Shahid M, Khan A, Adhikari A, Hannan PA, et al. Pharmacological screening of Monotheca buxifolia
(Falc) A. DC. for antinociceptive anti-inflammatory and antipyretic activities. BMC Complem Altern Med
Hämäläinen M, Nieminen R, Asmawi M, Vuorela P, Vapaatalo H, Moilanen E. Effects of flavonoids on prostaglandin E-2 production and on COX-2 and mPGES-1 expressions in activated macrophages. Planta Med
Xu Y, Wang C, Wu L, Li Z, Chen M, Wang Y, et al. Comparison of inhibitory effects of nine flavonoids on prostaglandin E2
production and COX-2 expression in LPS-stimulated RAW264.7 macrophages. Int Conf Biomed Eng Biotechnol
Sakamoto W, Fujie K, Nishihira J, Mino M, Morita I, Murota SI. Inhibition of PGE2
production in macrophages from vitamin E-treated rats. Prostaglandins Leukot Essent Fatty Acids
Ferrario A, Luna M, Rucker N, Wong S, Gomer CJ. Pro-apoptotic and anti-inflammatory properties of the green tea constituent epigallocatechin gallate increase photodynamic therapy responsiveness. Lasers Surg Med
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]