Efficacy of Trigonella foenum-graecum Seed Extract in Reducing Metabolic and Inflammatory Alterations Associated With Menopause
Abstract
Background:
Several experimental and clinical studies support beneficial effects of Trigonella foenum-graecum (fenugreek) in the management of metabolic diseases and inflammatory disorders.
Objectives:
The purpose of this study was to examine the effect of T. foenum-graecum seed extract in reducing the metabolic and inflammatory alternations associated with menopause.
Materials and Methods:
In this experimental study, 49 rats were divided into seven groups: (I) sham-control, (II) ovariectomized-control, (III and IV) ovariectomized treated with 50 and 150 mg/kg of T. foenum-graecum seed ethanolic extract, (V and VI) ovariectomized treated with 50 and 150 mg/kg of T. foenum-graecum hexanic extract, (VII) ovariectomized-positive control treated with 10 µg/kg of estradiol. The extracts were injected intraperitoneally one day after ovariectomy and the treatments were lasted for 42 days.
Results:
Fasting blood glucose and body weight gain increased significantly in the ovariectomized-control group compared with that in the sham animals (P < 0.05). Administration of estradiol and T. foenum-graecum (50 and 150 mg/dL of hexanic extract and 150 mg/kg of ethanolic extract) significantly diminished the increase in glucose and body weight (P < 0.05). The serum level of interleukin-1 (IL-1), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) in the ovariectomized control group was significantly higher than those in the sham animals (P < 0.05). Both hexanic and ethanolic extracts as well as estradiol were able to decrease level of these cytokines in the serum of ovariectomized rats (P < 0.05).
Conclusions:
The results of the present study show that administration of T. foenum-graecum corrects metabolic and inflammatory alterations associated with ovariectomy and has a potential for the management of menopause.
1. Background
Menopause is associated with increased risk of metabolic diseases such as type 2 diabetes and metabolic syndrome (1, 2). Dyslipidemia, obesity, and insulin resistance are of the most common features of the metabolic syndrome in menopausal woman and known to be important risk factors for cardiovascular diseases (3-5). Menopause is also associated with a wide range of changes in the expression and secretion of proinflammatory cytokines which may explain increased incidence of osteoporosis, Alzheimer, arthritis, and other inflammatory diseases seen in a postmenopausal period (6-9).
For many years, hormone therapy was the first primary treatment modality for the management of menopause; however, it had own limitations like increasing risk of stroke, coronary heart disease, pulmonary embolism, and ovarian cancer (1, 10). Therefore, development of new agents with anti-inflammatory action and lesser side effects for management of menopause remains an attractive subject. It has been reported that a number of medicinal plants may be useful for preventing or treating some menopausal related complications such as insulin resistance, dyslipidemia, hepatic steatosis, weight gain, inflammation, and loss of bone mass (11-13).
Trigonella foenum-graecum (fenugreek), a plant of Fabaceae family, has a long history for management of diabetes and dyslipidemia (14, 15). Several studies also support anti-inflammatory and immunomodulatory activities of T. foenum-graecum in adult male animals (16-18). Recently, Sindhu et al. (19) reported that mucilage extracted from ethanolic extract (EE) of T. foenum graecum has anti-inflammatory and antioxidative properties on adjuvant-induced arthritis in female rats. Further, Hakimi et al. showed that T. foenum graecum seed decreases the number of hot flashes and vasomotor symptoms in menopausal women (20). However, to the best of our knowledge, no study has yet evaluated the effect of this plant on the level of proinflammatory cytokines in menopause.
2. Objectives
The present work was performed to investigate the effects of chronic treatment with T. foenum graecum seed extracts on serum concentration of interleukin-1 (IL-1), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) in ovariectomized rats.
3. Materials and Methods
3.1. Plant Material and Extraction
The seeds of T. foenum-graecum were purchased from local market (Guilan, Iran) and identified at the herbarium of Agricultural Research Center of Guilan University (Iran). The EE and Hexanic Extract (HE) of T. foenum-graecum were prepared using a maceration method as described previously (21, 22). Briefly, the air-dried powder of the seeds was suspended in 96% ethanol (5 mL per g of seed) and maintained for 72 hour at 37°C. Then the solvent was removed and a new extraction started again with fresh ethanol. This step was repeated once more to get the best extraction efficiency. Finally, the EE was filtered through Whatman No.1 filter paper and dried using a rotary vacuum evaporator (GLF, Germany) at 50°C. The HE was prepared with the same procedure as for the EE.
3.2. Animals
Female Wistar rats initially weighing 190 to 220 g were obtained from Pasteur Institute, Hesarak Branch, Iran. The animals were maintained at 22°C ± 4°C on a light/dark cycle of 12 hour and away from stress. At all stages of the study, they had free access to enough laboratory chow and tap water ad libitum. Ethical rules of working with laboratory animals were approved by Guilan University of Medical Sciences.
3.3. Experimental Design
This work was an experimental study. After two weeks acclimatization period, animals were randomly divided into the following 7 experimental groups, each group including 7 animals: group I included sham control rats; group II comprised ovariectomized control animals; groups III and IV included ovariectomized animals and administrated intraperitoneally EE of T. foenum-graecum (50 and 150 mg/kg, respectively); groups V and VI comprised ovariectomized animals and treated intraperitoneally HE of T. foenum-graecum (50 and 150 mg/kg, respectively); groups VII included ovariectomized positive control rats, which administrated orally 10 µg/kg of 17-β estradiol valerate (Aburaihan Pharmaceutical Co., Iran). The treatments were started one day after removal of ovaries and lasted for 42 days. During this period, animals in the sham control and ovariectomized control groups received saline as a vehicle. Fasting Blood Glucose (FBG) and body weight of all of the rats were recorded prior to the start and at the end of treatments.
3.4. Ovariectomy Surgery
After an overnight fast, each rat was anesthetized with intraperitoneally injection of 320 mg/kg chloralhydrate (Arya Pharmaceutical Co., Iran) (23). Then, a small abdominal skin incision was performed and after exposing ovaries, they were removed bilaterally and tubal ends were closed using 2/0 silk string to prevent internal bleeding. Then the fat pad was repositioned into the abdomen and muscle and skin were connected by 2/0 chromic catgut sutures in two layers. The animal was placed in a warm place to come intellect. The animals in the control group underwent a similar procedure without eliminating the ovaries.
3.5. Biochemical Assays
At the end of the 42th day, blood sample was collected from tail vein of fasted animals for biochemical assays. The samples were centrifuged for 5 minutes at 3000 rpm and supernatants were maintained at -20°C for further analysis. The level of FBG was determined using Accu-check glucometer (Roche Diagnostic, Germany). Concentrations of IL-1, IL-6 and TNF-α were measured by E0071Ra, E90079Ra, and E90133Ra Elisa kit, respectively (Life Science Inc, China).
3.6. Statistical Analysis
Differences between means of different groups were analyzed using one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test for multiple comparisons. Paired t-test was used to compare the differences between day 0 and day 42. The P-values less than 0.05 were considered to be statistically significant. Results were exhibited as the Mean ± Standard Error of the Mean (SEM).
4. Results
4.1. Effects of T. foenum-graecum on Blood Glucose and Body Weight
In nonovariectomized sham group, the mean FBG on day 0 (5.72 ± 0.12 mmol/L) and day 42 (5.38 ± 0.11 mmol/L) was not significantly different. On the other hand, concentration of FBG at the end of the study was significantly higher than day 0 in ovariectomized control animals (6.16 ± 0.13 mmol/L vs. 8.77 ± 0.47 mmol/L, P < 0.05). Although the administration of estradiol or T. foenum-graecum (50 and 150 mg/dl of HE and 150 mg/kg of EE) to ovariectomized animals significantly diminished (P < 0.05) the increase of FBG, in all treated groups the level of FBG was still higher than that of day 0 (Table 1).
Effects of Trigonella foenum-graecum on Body Weight and Fasting Blood Glucose of Ovariectomized Ratsa,b
| Animal Groups | Blood Glucose, mmol/L | Weight Gain During 42 days, g | |
|---|---|---|---|
| Day 0 | Day 42 | ||
| Control | 5.72 ± 0.12 | 5.38 ± 0.11 | 53 ± 9c |
| OVA + Saline | 6.16 ± 0.13 | 8.77 ± 0.47 | 111 ± 7 |
| OVA + Estradiol | 5.88 ± 0.14 | 7.44 ± 0.32 | 58 ± 6c |
| OVA + HE 50 mg/kg | 5.22 ± 0.13 | 7.33 ± 0.16 c,d | 66 ± 8c |
| OVA + HE 150 mg/kg | 5.5 ± 0.13 | 7.11 ± 0.18 c,d | 64 ± 7c |
| OVA + EE 50 mg/kg | 5.61 ± 0.14 | 7.5 ± 0.15 d | 81 ± 8d |
| OVA + EE 150 mg/kg | 4.94 ± 0.13 d | 7.16 ± 0.15 c,d | 74 ± 9c |
aAbbreviations: EE, ethanolic extract; HE, hexanic extract; and OVA, ovariectomy.
bValues are expressed as Mean ± SEM (n = 7).
cP < 0.05 vs. OVA + Saline.
dP < 0.05 vs. Day 0 at the corresponding group.
There was a significant difference regarding weight gain between the sham control (53 ± 9 g) and ovariectomized control groups (111 ± 7 g, P < 0.05). Estradiol and both extracts of T. foenum-graecum significantly decreased the body-weight gain compared to the ovariectomized control group (P < 0.05).
4.2. Effects of T. foenum-graecum on ProinflammatoryCytokines
As shown in Figure 1, the serum IL-1 level of the saline-injected rats in the ovariectomized group was significantly higher than those of the sham animals (990 ± 2.9 vs. 300 ± 2.8 pg/mL, P < 0.05). Administration of both HE and EE of T. foenum-graecum significantly decreased serum IL-1 in the ovariectomized rats compared to the saline group (P < 0.05). The level of IL-1 in groups received 50 and 150 mg/kg of HE was 440 ± 2.8 pg/mL and 410 ± 2.2 pg/mL, respectively. Also, concentrations of IL-1 in animals treated with 50 and 150 mg/kg of EE were 410 ± 2.2 pg/mL and 610 ± 2.7 pg/mL, respectively. The effect of HE was comparable to that of induced by 10 µg/kg of estradiol (389 ± 2.9 pg/mL).
Effect of Trigonella foenum-graecum on Concentration of Interlukin-1 in Blood of the Ovariectomized Rats
The animals were subjected to ovariectomy surgery and then treated intraperitoneally with 10 µg/kg estradiol or concentrations of 50 mg/kg and 150 mg/kg of HE and EE of T. foenum-graecum seeds for 6 weeks. Values are expressed as Mean ± SEM (n = 7). *P < 0.05 vs. control group; #P < 0.05 vs. saline group.
Similarly, serum IL-6 significantly increased in ovariectomized control group when compared to the sham animals (1258 ± 2.7 vs. 483 ± 3 pg/mL, P < 0.05). As shown in Figure 2, hexanic and ethanolic extracts of T. foenum-graecum, like estradiol, diminished the IL-6 level in ovariectomized animals (P < 0.05 as compared with saline group). Treatment with 50 and 150 mg/kg of HE was also able to significantly decrease serum TNF-α from 999 ± 2.4 pg/mL (saline group) to 457 ± 2.5 and 445 ± 2.6 pg/mL, respectively, comparable to the effect of estradiol (430 ± 2.6 pg/mL). A similar decrease in TNF-α concentration was induced by both doses of EE (Figure 3).
Effect of Trigonella foenum-graecum on Concentration of Interlukin-6 in Blood of Ovariectomized Rats
The animals were subjected to ovariectomy surgery and then treated intraperitoneally with 10 µg/kg estradiol or concentrations of 50 mg/kg and 150 mg/kg ofHE and EE of T. foenum-graecum seeds for 6 weeks. Values are expressed as Mean ± SEM (n = 7). *P < 0.05 vs. control group; #P < 0.05 vs. saline group.
Effect of Trigonella foenum-graecum on Concentration of Tumor Necrosis Factor-α in Blood of Ovariectomized Rats
The animals were subjected to ovariectomy surgery and then treated intraperitoneally with 10 µg/kg estradiol or concentrations of 50 mg/kg and 150 mg/kg of HE and EE of T. foenum-graecum seeds for 6 weeks. Values are expressed as Mean ± SEM (n = 7). *P < 0.05 vs. control group; #P < 0.05 vs. saline group.
5. Discussion
The prevalence of metabolic syndrome and inflammatory diseases increases during menopause with the overproduction of proinflammatory cytokines. The present study showed that both HE and EE of T. foenum-graecum seed are able to improve metabolic status and decrease level of these cytokines in ovariectomized rats. Ovariectomy is a standard experimental model of menopause in rodent to investigate pharmacological management of postmenopausal symptoms (11, 12, 24, 25). In our study, in agreement with previous reports, ovariectomy led to increased body weight gain (25, 26). This increase of body weight was accompanied by a significant raise of blood glucose. Administration of estradiol could diminish the increase of both body weight and FBG. Similarly, Abbas and Elsamanoudy observed that estradiol decreases FBG, fasting insulin, and Homeostatis Model Assessment of Insulin Resistance (HOMA-IR, a predictor of insulin sensitivity) in ovariectomized rats (24). The beneficial effects of estradiol on glucose homeostasis and body weight were mimicked by T. foenum-graecum. Hypoglycemic effect of T. foenum-graecum has been demonstrated previously in several experimental and clinical studies (27). This effect may be achieved by inhibition of intestinal glucose absorption, enhancing insulin actions on tissues, and activation of hepatic enzymes (28, 29). The inhibitory effect of T. foenum-graecum on weight gain of ovariectomized rats may be related to improvement of insulin resistance. This is in consistent with previous reports that T. foenum-graecum reduces the body weight gain and hyperlipidaemia induced by high-fat diet (30, 31).
As reported by other researchers, in our study ovariectomy led to increased level of proinflammatory cytokines. The mechanism underlying elevated inflammation markers in postmenopausal period is not exactly clear; however, excess production of cytokines by fat and bone marrow can be involved (4, 32). The cytokines TNF-α, IL-1, and IL-6 have obtained the most attention due to their prominent causal role in postmenopausal inflammatory diseases (7, 33). In this work, estradiol replacement could restore the level of these cytokines to near that of control animals. The mechanisms by which estrogen modulates the level and activity of cytokines may include alterations of immune cell function, antioxidative actions, and changes in nitric oxide activity (6, 32, 33). Similar mechanisms may describe an inhibitory effect of T. foenum-graecum on the level of TNF-α, IL-1, and IL-6. It has been reported that this plant has estrogenic activities in vitro (34). The presence of phytoestrogen compounds like diosgenin in T. foenum-graecum may be responsible for this estrogenic effect (35). On the other hand, several studies have shown that T. foenum-graecum has antioxidative, anti-inflammatory, and immunomodulatory activities in male and female animals (16-19). For example, it was demonstrated that diosgenin induces anti-inflammatory action in adipose tissue (36). Sindhu et al. reported that EE of T. foenum graecum decreases the blood levels of IL-1, IL-2, IL-6, and TNF-α in female rat model of arthritis (19) Also, treatment with hydroalcoholic extract of T. foenum graecum seed reduces oxidative stress and the proinflammatory cytokines TNF-α and IL-6 in diabetic rats (37). Further, it has been reported that improvement in glucose metabolism with weight loss is independently associated with reduction of cytokine levels (38).
In this study, we used EE and HE of T. foenum-graecum to test beneficial effects of this plant in the management of metabolic and inflammatory alterations associated with menopause. For extraction of plant materials, the solvents are chosen based on their selectivity for the compounds to be extracted. Nonpolar solvent such as hexane is used to extract lipophilic constituents (e.g. fatty acids, alkanes, sterols, coumarins, and some terpenoids). Solvents with medium-polarity such as ethyl acetate are used to extract constituents with intermediate polarity (e.g. flavonoids and some alkaloids). A more polar solvent such as ethanol is used to extract more polar constituents (e.g. tannins and glycosides) (39, 40). Interestingly, in our experiment, both EE and HE of T. foenum-graecum could correct metabolic and inflammatory alterations induced by ovariectomy (although the HE showed stronger effects). Therefore, it can be concluded that both polar and nonpolar constituents of T. foenum-graecum are involved in the beneficial effects of this plant. Diosgenin, a steroid saponin with anti-inflammatory, antioxidative, and estrogenic properties, may be of the candidate constituents responsible for the above-mentioned effects of T. foenum-graecum (31, 35, 36). Further works on isolation and characterization of active compound of the plant would be of interest.
This study described observations on the effect of T. foenum-graecum on metabolic and inflammatory alterations in a rat model of menopause, which may not mimic human menopause. Therefore, well-planned clinical studies on this topic are needed. Another limitation of the present work is the failure to address exact compound responsible for the effects of T. foenum-graecum. Also, long-term safety and potential adverse effects of T. foenum-graecum in menopause women should be well-defined.
In conclusion, the present study showed that the administration of T. foenum-graecum improves metabolic features, and corrects inflammatory alterations associated with ovariectomy and thus has a potential for management of menopause.
Footnotes
Authors’ Contribution:Mahmood Abedinzade and Sima Nasri designed the study and collected data. Masome Jamal Omodi and Elham Ghasemi collected data. Ahmad Ghorbani performed the statistical analysis, managed the literature searches and wrote the first draft of the manuscript. All authors read and approved the final version of the manuscript.
Funding/Support:This work was financially supported by Guilan University of Medical Sciences, Rasht, IR Iran.
Acknowledgments
We would like to highly appreciate the kind cooperation of Dr. Babaei.
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