Sat, Nov 30, 2024
[Archive]
Volume 2, Issue 4 (Nov 2017)
JNFS 2017, 2(4): 300-307 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Mousavi S N, Jazayeri S, Khoshpay B, Malek M, Hosseini A F, Hosseini S et al . Royal Jelly Decreases Blood Pressure, Serum Glucose, and Interleukin-6 in Patients with Type 2 Diabetes on an Iso-caloric Diet. JNFS 2017; 2 (4) :300-307
URL: http://jnfs.ssu.ac.ir/article-1-113-en.html
URL: http://jnfs.ssu.ac.ir/article-1-113-en.html
Seyedeh Neda Mousavi 
, Shima Jazayeri , Basmeh Khoshpay , Mojtaba Malek , Agha Fatemeh Hosseini , Sharieh Hosseini , Farzad Shidfar *
, Shima Jazayeri , Basmeh Khoshpay , Mojtaba Malek , Agha Fatemeh Hosseini , Sharieh Hosseini , Farzad Shidfar *
Research Center for Prevention of Cardiovascular Disease, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran
Full-Text [PDF 605 kb]
(1821 Downloads)
| Abstract (HTML) (3543 Views)
Introduction
both of them leads to insulin resistance,
endothelial dysfunction, and finally cardiovascular complications. Obesity, as a common feature of diabetic patients is associated with more generalized systemic inflammation involving circulating inflammatory proteins such as C-reactive protein (CRP), Interleukin-6 (IL-6), plasminogen activator inhibitor (PAI-1), P-selection, vascular cell adhesion molecule (VCAM-1), and fibrinogen. Adhesion molecule expression is induced by pro-inflammatory cytokines such as IL-1β, tumor necrosis factor (TNF-α), and CRP produced by the liver in response to IL-6 (Van Gaal et al., 2006). Insulin resistance and type 2 diabetes are associated with several changes in lipids and lipoproteins (Garvey et al., 2003).
Totally, high blood pressure, insulin resistance, and inflammation are the most important risk factors of CVDs in patients with T2DM. Therefore, it is important to recognize and treat these conditions to postpone or even prevent from CVDs incidence in T2DM patients.
More diabetic patients use complementary and alternative medicine (CAM). Royal jelly (RJ) as a bee product is secreted from the hypopharingeal and mandibular glands of the worker bees. It is a popular traditional food containing proteins, sugar, and fatty acids (10-hy-droxy-2-decenoic acid) (Tokunaga et al., 2004). Hypotensive activity, insulin-like action, antitumor activity, and vasodilation are some pharmacological functions of RJ (Tokunaga et al., 2004).
One study indicated that peptides consuming
RJ can reduce blood pressure by inhibiting the activity of angiotensin converting enzyme (ACE) (Maruyama et al., 2005). In one study, researchers showed the anti-inflammatory actions of RJ at the cytokine level. Furthermore, it was represented that it can reduce the production of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1) in a dose- response manner.
Some factors in RJ can inhibit secretion of pro-inflammatory cytokines (Kohno et al., 2004). In another study, researchers assessed the effects of RJ consumption on blood glucose levels in healthy participants. Blood glucose and area under the curve were significantly reduced after RJ supplementation (Münstedt et al., 2009). Hyperglycemia is an initiation of tissue destruction in DM and high blood pressure can worse the blood glucose levels (Brownlee, 2005). To the best of our knowledge, this is the first human study in which the effect of RJ supplementation is evaluated on serum glucose, IL-6, glycosylated hemoglobin (HbA1c), and blood pressure in T2DM patients. It is hypothesized that RJ supplementation improves serum glucose, IL-6, HbA1c, systolic, and diastolic blood pressure (SBP and DBP) in T2DM patients through decrease of insulin resistance.
Materials and Methods
Study design and participants: In designing the study, power of 90% with a two-sided test and α = 0.05 (type I error) were considered to detect a 5% difference in serum glucose between the two groups. On the basis of SDs, the values reported in a similar study were used (Hang et al., 2007). The number of participants needed to detect this difference was 20 in each group. Given an anticipated drop-out rate of 25 %, the enrollment target was set at 25 individuals. The double-blinded randomized controlled trial (RCT) was conducted in the Endocrine and Metabolism Institute of Iran University of Medical Sciences to assess the RJ effects on serum glucose, IL-6, SBP, DBP, and HbA1c in T2DM patients The inclusion criteria consisted of: (1) being in the age range of 25-65 years, (2) having BMI of 26-30 kg/m2, (3) Iranian ethnicity, (4) diagnosed type 2 diabetes for 5-10 years, (5) HbA1c of 7-9%, and (6) receiving oral hypoglycemic drugs. The exclusion criteria included: (1) serum triglyceride level (TG) > 400 mg/dL, serum cholesterol level > 240 mg/dL, (2) lactating or pregnancy, (3) diagnosis of heart, liver, and renal failure, cancer, acute myocardial infarction, stroke, or serious injuries, (4) receiving multivitamin or antioxidant supplements at least 3 months, (5) smoking/alcohol consumption, (6) taking oral contraceptive or lipid lowering drugs, (7) insulin infusion, (8) allergy to RJ, (9) any mal-absorption diseases such as celiac or steatorrhea, and (10) athletes. The study was approved by the Bioethics Committee of Iran University of Medical Sciences. Totally, 46 patients were randomly assigned into two groups; Group RJ (RJG) received 1000 mg of the RJ supplements (Natural life. Frengrove Co. Australia) three times daily and placebo group (PG) received1000 mg of exactly the same placebo (as glycerin) (Pars Minoo Inc. Tehran Iran) three times daily for up to 8 weeks. Shape, color, and package of the placebo were similar to the RJ. Products were administered by a blinded researcher assistant to the patients. First, RJ and placebo were divided into similar packages for one week intake. Then, residuals of each package were assessed to determine the compliance of the patients. In this regard, participants with the compliance rate below 80% were excluded from the study. Those who entered the study were randomly assigned to one of the two groups via computer-generated numbers. Both active and placebo treatments were contained in the same opaque capsules and side effects of supplements were recorded.
Participants were instructed to maintain an isocaloric diet, continue their previous eating habits under the supervision of an experienced nutritionist, and not to change their routine physical activities during the study period. Throughout the study period, individuals were directed to continue taking the same dose of any prescribed hypoglycemic agents unless hypoglycemia occurred; in this case they were directed to reduce their dose immediately.
Measurements: Daily food intake was obtained by a 24-hour dietary recall questionnaire and physical activity level by International Physical Activity Questionnaire (IPAQ) questionnaire in three days (two regular days and one holiday) at the beginning and end of the study. These dietary intake data were analyzed by the Nutritionist 4 (N4) software (Nutritionist 4, First Data Bank, San Bruno, CA, USA).
Fasting blood samples were collected at the baseline and 8 wk after the intervention. Serum glucose was used as the major outcome measurement. Moreover, SBP, DBP, HbA1c, and IL-6 levels were assessed for both groups at the baseline and end of the study. Serum glucose was measured by an enzymatic method (Pars Azmon Co. kit, Tehran, Iran) using Liasys autoanalyzer. Later, HbA1c was measured by HPLC and IL-6 by ELISA method (BD bio science Co. kit, USA). Nutritional data were obtained via 24 hour diet recall. Participants' weight was also measured on a calibrated balance Seca scale to the nearest 0.5 kg, followed by the demographic data collected at the initiation of the study.
Data analysis: Statistical analyses were performed through SPSS16 software (version 16; IBM Corp., USA). Normal distribution of variables was checked by Kolmogorov Smirnov Test; independent samples t-test was then used to test whether the differences between the mean values of the items studied in both groups were significant or not. Paired sample t-test was applied to evaluate differences before and after the intervention in each group. All data were expressed by means ± SD. The level of significance was determined at P-value < 0.05.
Ethical consideration: All experiments were conducted in accordance with the Declaration of Helsinki and all procedures were carried out while participants were totally aware of them and signed written consents. This study has also been registered at the Iranian registry of clinical trials (www.irct.ir) with IRCT number: IRCT201103012709N18).
Results
Demographic and anthropometric measurements at the baseline: The participants' demographic information through the intervention is shown in figure 1. There were 45.4% and 48% male participants in the RJ and placebo groups, respectively. Participants' gender was not significantly different between the two groups. Mean weight of participants was neither significantly different between the RJP and PG at the baseline (75.6 ± 10.2 kg vs. 74.1 ± 11.3 kg, respectively), nor at the end of the study (75.4 ± 10.1 kg vs. 73.9 ± 11.02 kg, respectively). Changes of weight mean from the baseline to the end were not significantly different between the two groups. Weight of participants was also not significantly different in each group before and after the intervention. Mean and standard deviation of nutrients' intake data are shown in Table 1.
There was no significant difference within and between the two groups for intake of energy and nutrient before and after the intervention. The level of physical activity and lipid lowering drugs were not different between the two groups at the baseline. No side effects were observed from
supplements in the participants.
Laboratory analysis measurements: As it is shown in Table 2, there was no significant difference in serum glucose, IL-6, HbA1c, SBP, DBP, and IL-6 between the two groups before the intervention. Serum glucose (P = 0.006), SBP (P = 0.02), and IL-6 (P = 0.017) decreased compared with the initial values at the end of the study in RJG. There were significant differences in mean changes from the baseline to endpoint of SBP (P = 0.006) between the two groups. There was no significant difference after RJ supplementation compared to previous values in serum glucose, HbA1c, and DBP.
References
Full-Text: (1295 Views)
Royal Jelly Decreases Blood Pressure, Serum Glucose, and Interleukin-6 in Patients with Type 2 Diabetes on an Iso-caloric Diet
Seyedeh Neda Mousavi; PhD1, Shima Jazayeri; PhD2, Basmeh Khoshpay, MSc2, Mojtaba Malek; MD3,
Agha Fatemeh Hosseini; PhD4, Sharieh Hosseini; PhD5 & Farzad Shidfar; PhD 2,6*
1 Department of Biochemistry and Nutrition, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
2 Department of Nutrition, School of Health, Iran University of Medical Sciences, Tehran, Iran.
3 Endocrine Research Center Institute of Endocrinology and Metabolism, Firouzgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
4 Department of Statistic, School of Health, Iran University of Medical Sciences, Tehran, Iran.
5Department of Applied Chemistry, School of Pharmaceutical Chemistry, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran.
6Research Center for Prevention of Cardiovascular Disease, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran.
Seyedeh Neda Mousavi; PhD1, Shima Jazayeri; PhD2, Basmeh Khoshpay, MSc2, Mojtaba Malek; MD3,
Agha Fatemeh Hosseini; PhD4, Sharieh Hosseini; PhD5 & Farzad Shidfar; PhD 2,6*
1 Department of Biochemistry and Nutrition, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
2 Department of Nutrition, School of Health, Iran University of Medical Sciences, Tehran, Iran.
3 Endocrine Research Center Institute of Endocrinology and Metabolism, Firouzgar Hospital, Iran University of Medical Sciences, Tehran, Iran.
4 Department of Statistic, School of Health, Iran University of Medical Sciences, Tehran, Iran.
5Department of Applied Chemistry, School of Pharmaceutical Chemistry, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran.
6Research Center for Prevention of Cardiovascular Disease, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran.
| ARTICLE INFO | ABSTRACT | |
| ORIGINAL ARTICLE | Background: Royal Jelly (RJ) is a mixture of protein, glucose, lipid, vitamins, and minerals that is widely used as a commercial medical product. Previous studies have shown that RJ has physiological effects such as anti-inflammatory, anti-tumor, anti-allergic, and antioxidant. In the present study, the effects of RJ on some cardiovascular disease risk factors were investigated in patients with type 2 diabetes on an iso-caloric diet. Methods: In this randomized controlled trial, patients with type 2 diabetes aged 25-65 years with body mass index (BMI) of 26-30 kg/m2 and hemoglobin A1c (HbA1c) of 7-9% were included. The patients were randomly assigned to receive 1000 mg of RJ supplement or the placebo three times daily for 8 wks. Weight, fasting blood glucose (FBG), HbA1c, blood pressure, and inteleukin-6 levels were measured. Results: In comparison to the placebo, FBG (P = 0.006), interleukin-6 (P = 0.017), and systolic blood pressure (P = 0.02) were significantly decreased in the RJ group at the end of the study. There were significant differences in the mean changes of systolic blood pressure at the baseline to the endpoint of systolic blood pressure between the two groups (P = 0.006). Conclusions: Royal Jelly may reduce incidence of cardiovascular disease by lowering effects on FBG, inteleukin-6, and systolic blood pressure in patients with type 2 diabetes. Keywords: Royal jelly; Interleukin-6; Blood pressure; Type 2 diabetes |
|
| Article history: Received: 18 Feb 2017 Revised: 14 Mar 2017 Accepted: 22 Apr 2017 |
||
| IRCT code: IRCT201103012709N18 | ||
| *Corresponding author: shidfar.f@iums.ac.ir Department of Nutrition, School of Health, Iran University of Medical Sciences, Tehran, Iran. Postal code: 1449614535 Tel: +98 21 88779118 |
Introduction
| Diabetes mellitus (DM), defined by elevated glycemic markers, is a major risk factor for cardiovascular diseases (CVDs). Cardiovascular diseases are the most common cause of death among adults with DM underscoring the need for aggressive CVDs risk factor management (Go et al., 2013). Insulin resistance occurs in several tissues. Hyperglycemia increases the risk of atherothombosis through several potential mechanisms (Laakso, 1999). Low-grade inflammation is linked to insulin resistance and involved in the pathogenesis of type 2 diabetes mellitus (T2DM) (Dandona et al., 2003). The signaling pathways of inflammation and insulin are tightly linked so that presence of defects in |
both of them leads to insulin resistance,
endothelial dysfunction, and finally cardiovascular complications. Obesity, as a common feature of diabetic patients is associated with more generalized systemic inflammation involving circulating inflammatory proteins such as C-reactive protein (CRP), Interleukin-6 (IL-6), plasminogen activator inhibitor (PAI-1), P-selection, vascular cell adhesion molecule (VCAM-1), and fibrinogen. Adhesion molecule expression is induced by pro-inflammatory cytokines such as IL-1β, tumor necrosis factor (TNF-α), and CRP produced by the liver in response to IL-6 (Van Gaal et al., 2006). Insulin resistance and type 2 diabetes are associated with several changes in lipids and lipoproteins (Garvey et al., 2003).
Totally, high blood pressure, insulin resistance, and inflammation are the most important risk factors of CVDs in patients with T2DM. Therefore, it is important to recognize and treat these conditions to postpone or even prevent from CVDs incidence in T2DM patients.
More diabetic patients use complementary and alternative medicine (CAM). Royal jelly (RJ) as a bee product is secreted from the hypopharingeal and mandibular glands of the worker bees. It is a popular traditional food containing proteins, sugar, and fatty acids (10-hy-droxy-2-decenoic acid) (Tokunaga et al., 2004). Hypotensive activity, insulin-like action, antitumor activity, and vasodilation are some pharmacological functions of RJ (Tokunaga et al., 2004).
One study indicated that peptides consuming
RJ can reduce blood pressure by inhibiting the activity of angiotensin converting enzyme (ACE) (Maruyama et al., 2005). In one study, researchers showed the anti-inflammatory actions of RJ at the cytokine level. Furthermore, it was represented that it can reduce the production of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1) in a dose- response manner.
Some factors in RJ can inhibit secretion of pro-inflammatory cytokines (Kohno et al., 2004). In another study, researchers assessed the effects of RJ consumption on blood glucose levels in healthy participants. Blood glucose and area under the curve were significantly reduced after RJ supplementation (Münstedt et al., 2009). Hyperglycemia is an initiation of tissue destruction in DM and high blood pressure can worse the blood glucose levels (Brownlee, 2005). To the best of our knowledge, this is the first human study in which the effect of RJ supplementation is evaluated on serum glucose, IL-6, glycosylated hemoglobin (HbA1c), and blood pressure in T2DM patients. It is hypothesized that RJ supplementation improves serum glucose, IL-6, HbA1c, systolic, and diastolic blood pressure (SBP and DBP) in T2DM patients through decrease of insulin resistance.
Materials and Methods
Study design and participants: In designing the study, power of 90% with a two-sided test and α = 0.05 (type I error) were considered to detect a 5% difference in serum glucose between the two groups. On the basis of SDs, the values reported in a similar study were used (Hang et al., 2007). The number of participants needed to detect this difference was 20 in each group. Given an anticipated drop-out rate of 25 %, the enrollment target was set at 25 individuals. The double-blinded randomized controlled trial (RCT) was conducted in the Endocrine and Metabolism Institute of Iran University of Medical Sciences to assess the RJ effects on serum glucose, IL-6, SBP, DBP, and HbA1c in T2DM patients The inclusion criteria consisted of: (1) being in the age range of 25-65 years, (2) having BMI of 26-30 kg/m2, (3) Iranian ethnicity, (4) diagnosed type 2 diabetes for 5-10 years, (5) HbA1c of 7-9%, and (6) receiving oral hypoglycemic drugs. The exclusion criteria included: (1) serum triglyceride level (TG) > 400 mg/dL, serum cholesterol level > 240 mg/dL, (2) lactating or pregnancy, (3) diagnosis of heart, liver, and renal failure, cancer, acute myocardial infarction, stroke, or serious injuries, (4) receiving multivitamin or antioxidant supplements at least 3 months, (5) smoking/alcohol consumption, (6) taking oral contraceptive or lipid lowering drugs, (7) insulin infusion, (8) allergy to RJ, (9) any mal-absorption diseases such as celiac or steatorrhea, and (10) athletes. The study was approved by the Bioethics Committee of Iran University of Medical Sciences. Totally, 46 patients were randomly assigned into two groups; Group RJ (RJG) received 1000 mg of the RJ supplements (Natural life. Frengrove Co. Australia) three times daily and placebo group (PG) received1000 mg of exactly the same placebo (as glycerin) (Pars Minoo Inc. Tehran Iran) three times daily for up to 8 weeks. Shape, color, and package of the placebo were similar to the RJ. Products were administered by a blinded researcher assistant to the patients. First, RJ and placebo were divided into similar packages for one week intake. Then, residuals of each package were assessed to determine the compliance of the patients. In this regard, participants with the compliance rate below 80% were excluded from the study. Those who entered the study were randomly assigned to one of the two groups via computer-generated numbers. Both active and placebo treatments were contained in the same opaque capsules and side effects of supplements were recorded.
Participants were instructed to maintain an isocaloric diet, continue their previous eating habits under the supervision of an experienced nutritionist, and not to change their routine physical activities during the study period. Throughout the study period, individuals were directed to continue taking the same dose of any prescribed hypoglycemic agents unless hypoglycemia occurred; in this case they were directed to reduce their dose immediately.
Measurements: Daily food intake was obtained by a 24-hour dietary recall questionnaire and physical activity level by International Physical Activity Questionnaire (IPAQ) questionnaire in three days (two regular days and one holiday) at the beginning and end of the study. These dietary intake data were analyzed by the Nutritionist 4 (N4) software (Nutritionist 4, First Data Bank, San Bruno, CA, USA).
Fasting blood samples were collected at the baseline and 8 wk after the intervention. Serum glucose was used as the major outcome measurement. Moreover, SBP, DBP, HbA1c, and IL-6 levels were assessed for both groups at the baseline and end of the study. Serum glucose was measured by an enzymatic method (Pars Azmon Co. kit, Tehran, Iran) using Liasys autoanalyzer. Later, HbA1c was measured by HPLC and IL-6 by ELISA method (BD bio science Co. kit, USA). Nutritional data were obtained via 24 hour diet recall. Participants' weight was also measured on a calibrated balance Seca scale to the nearest 0.5 kg, followed by the demographic data collected at the initiation of the study.
Data analysis: Statistical analyses were performed through SPSS16 software (version 16; IBM Corp., USA). Normal distribution of variables was checked by Kolmogorov Smirnov Test; independent samples t-test was then used to test whether the differences between the mean values of the items studied in both groups were significant or not. Paired sample t-test was applied to evaluate differences before and after the intervention in each group. All data were expressed by means ± SD. The level of significance was determined at P-value < 0.05.
Ethical consideration: All experiments were conducted in accordance with the Declaration of Helsinki and all procedures were carried out while participants were totally aware of them and signed written consents. This study has also been registered at the Iranian registry of clinical trials (www.irct.ir) with IRCT number: IRCT201103012709N18).
Results
Demographic and anthropometric measurements at the baseline: The participants' demographic information through the intervention is shown in figure 1. There were 45.4% and 48% male participants in the RJ and placebo groups, respectively. Participants' gender was not significantly different between the two groups. Mean weight of participants was neither significantly different between the RJP and PG at the baseline (75.6 ± 10.2 kg vs. 74.1 ± 11.3 kg, respectively), nor at the end of the study (75.4 ± 10.1 kg vs. 73.9 ± 11.02 kg, respectively). Changes of weight mean from the baseline to the end were not significantly different between the two groups. Weight of participants was also not significantly different in each group before and after the intervention. Mean and standard deviation of nutrients' intake data are shown in Table 1.
There was no significant difference within and between the two groups for intake of energy and nutrient before and after the intervention. The level of physical activity and lipid lowering drugs were not different between the two groups at the baseline. No side effects were observed from
supplements in the participants.
Laboratory analysis measurements: As it is shown in Table 2, there was no significant difference in serum glucose, IL-6, HbA1c, SBP, DBP, and IL-6 between the two groups before the intervention. Serum glucose (P = 0.006), SBP (P = 0.02), and IL-6 (P = 0.017) decreased compared with the initial values at the end of the study in RJG. There were significant differences in mean changes from the baseline to endpoint of SBP (P = 0.006) between the two groups. There was no significant difference after RJ supplementation compared to previous values in serum glucose, HbA1c, and DBP.
| Figure 1. Follow of participants through the intervention |
| Table 1. Comparison of dietary intake of energy, macronutrients and some micronutrients between the two groups | |||
| Dietary intake | RJ group (n=23) | Placebo group (n=23) | P-valuea |
| Total energy (Kcal/day) | |||
| Before After |
1685.69 ± 217.79 1716.95 ± 213.37 |
1770.04 ± 184.28 1730.65 ± 246.94 |
0.28 0.30 |
| Total protein (g/day) | |||
| Before After |
65.34 ± 8.93 69.32 ± 10.26 |
69.32 ± 10.26 65.25 ± 12.10 |
0.10 0.08 |
| Total carbohydrate (g/day) | |||
| Before After |
237.49 ± 30.93 240.37 ± 29.87 |
248.84 ± 28.91 242.29 ± 34.57 |
0.56 0.31 |
| Total fat (g/day) | |||
| Before After |
53.81 ± 10.76 55.84 ± 9.05 |
57.56 ± 9.72 53.65 ± 7.65 |
0.23 0.08 |
| Saturated fat (g/day) | |||
| Before After |
24.04 ± 5.15 22.04 ± 4.85 |
25.08 ± 4.14 24.30 ± 4.95 |
0.11 0.55 |
| Mono unsaturated fat (g/day) | |||
| Before After |
13.78 ± 3.69 14.73 ± 3.76 |
13.56 ± 4.81 12.95 ± 2.89 |
0.08 0.30 |
| Poly unsaturated fat (g/day) | |||
| Before After |
15.78 ± 3.46 16.56 ± 4.31 |
17.82 ± 3.91 16.06 ± 3.69 |
0.49 0.14 |
| Vitamin C (mg/day) | |||
| Before After |
77.53 ± 18.48 78.28 ± 18.81 |
74.22 ± 21.13 80.27 ± 18.51 |
0.87 0.10 |
| Vitamin E (mg/day) | |||
| Before After |
18.09 ± 5.09 17.67 ± 5.59 |
17.93 ± 7.05 14.43 ± 5.81 |
0.63 0.11 |
a: Student t-test, a: Paired t-test; b: Student t-test
| Table2. Camparison of mean (±SD) some cardiovascular disease risk factors within and between groups | |||||
| Variables | Group | Before | After | Change | P-value b |
| Glucose (mg/dL) | RJ Placebo |
128.4 ± 44.4 145.7 ± 48.4 |
119.0 ± 30.9 149.7 ± 40.2 |
-9.4 ± 26.0 4.0±30.4 |
0.09 0.53 |
| P-valuea | 0.2 | 0.006 | 0.11 | ||
| Hmoglobin bA1c (%) | RJ Placebo |
8.1 ± 4.1 7.4 ± 6.2 |
6.7 ± 2.2 8.6 ± 4.9 |
-1.45 ± 4.1 1.16 ± 5.1 |
0.33 0.95 |
| p value | 0.6 | 0.11 | 0.48 | ||
| Systolic blood pressure (mmHg) | RJ Placebo |
131.4 ± 10.2 136.1 ± 14.4 |
126.8 ±13.8 136.7 ± 14.1 |
-4.5 ± 8.0 0.6 ± 2.8 |
0.01 0.31 |
| p value | 0.2 | 0.02 | 0.006 | ||
| Dystolic blood pressure (mmHg) | RJ Placebo |
86.5 ± 8.5 86.1± 6.1 |
83.6 ± 3.9 86.2 ± 5.8 |
-2.9 ± 8.1 0.13 ± 1.2 |
0.09 0.6 |
| p value | 0.83 | 0.08 | 0.07 | ||
| Interleukin-6 (pg/ml) | RJ Placebo |
6.6 ± 3.3 6.6 ± 3.2 |
4.8 ± 1.4 6.1± 1.9 |
-1.79 ± 3.4 -0.51 ± 2.8 |
0.02 0.39 |
| p value | 0.99 | 0.017 | 0.18 | ||
Discussion
To the best of our knowledge, this is the first RCT conducted to assess the effects of RJ supplementation on the incidence of cardiovascular risk via measurement of serum glucose, IL-6, HbA1c, and blood pressure in T2DM patients. In this study, intake of RJ significantly reduced serum glucose, SBP, and IL-6 after the intervention but there were no significant differences before and after RJ supplementation in HbA1c and DBP. Some tests were carried out to confirm that RJ reduced the effects of diabetes on animals. The simultaneous administration of RJ and a fructose solution for 8 weeks to insulin-resistant rats significantly reduced plasmatic concentration of insulin, triglycerides, and SBP, without affecting the blood levels of glucose or total cholesterol. These results suggest that RJ can be a functional dietary treatment to prevent from insulin resistance associated with developing hypertension in diabetic patients (Nomura et al., 2007, Zamami et al., 2008). One clinical study demonstrated that RJ significantly affects serum glucose levels in healthy participants (Munstedt et al. 2009). It was reported in another study that RJ reduced the index of insulin resistance (HOMA-IR) but did not reduce blood glucose levels in rats (Zamami et al., 2008). In a recent study, researchers showed that RJ increased catalase activity and antioxidant power, while it decreased malondialdehyde levels in the kidney tissue homogenates of streptozotocin induced diabetic rats (Ghanbari et al., 2015). It has also been shown that RJ contains biologically active substances which causes insulin-like activity (Kramer et al., 1982). Elevated blood glucose level contributes to the proteins and lipid glycation, resulting in the formation of advanced glycation end-products (AGEs) (Pickup, 2004). Receptors for AGEs (RAGE) are expressed in many different tissues and cell types, including endothelial cells, vascular smooth muscle cells, and macrophages (Basta et al., 2004) that lead to the intracellular generation of ROS which activates NF-kB (Wendt et al., 2002). Then, the expression of TNF, IL 1, 6, 8, and 18 as well as interferon-γ (IFN-γ) are increased (Wautier et al., 2001). A clinical study suggests that acute hyperglycaemia can result in elevated levels of circulating inflammatory cytokines, in particular TNF-α, IL-6 and IL-18 (Basta et al., 2002). In one study, the anti-inflammatory actions of RJ at a cytokine level were examined. Supernatants of RJ suspensions were added to a culture of mouse peritoneal macrophages stimulated with lipopolysaccharide and IFN-γ. The production of proinflammatory cytokines such as TNF-α, IL-6, and IL-1 were efficiently inhibited in a dose-dependent manner without having cytotoxic effects on macrophages. This suggests that RJ contains factor(s) responsible for the suppression of proinflammatory cytokines secretion.
Researchers named the factor for honey-
bees, RJ-derived anti-inflammatory factor (HBRJ11AIF) and further investigated its molecular aspects. Size fractionation study showed that HBRJ-AIF is composed of substances of low (< 5 kDa) and high (> 30 kDa) molecular weights; the former is a major component. Chromatographic analysis showed that MRJP3 is one candidate for the HBRJ-AIF with high molecular weights. Thus, these results suggest that RJ has anti-inflammatory actions through inhibiting pro-inflammatory cytokine production by activated macrophages (Kohno et al., 2004). One study indicated that Protease N treated RJ (Pro-RJ) and peptides (IY, VY, IVY) from Pro-RJ, inhibited ACE activity and they have an antihypertensive effect in repeated oral administration for 28 days in spontaneously hypertensive rats (Tokunaga et al. 2004). Another study suggested that the trans-2-octenoic acid and the hydroxydecanoic acid from RJ may be responsible for the anti-hypertensive action, with different RJ fractions exercising bigger or smaller effects on the duration of the action (Librowski and Czarnecki, 2000).
Researchers investigated the anti-inflammatory effects of RJ in formalin-induced rat paw edema; they administered 25, 50, and 100 mg/kg, intera-peritoneal of RJ to these rats. The highest anti-inflammatory effect was observed in doses of 50 and 100 mg/kg (Arzi et al., 2015).
In one human study, researchers determined the effects of RJ supplementation on diabetic females. A single dose of 1000 mg RJ was used in this study. Means of fasting blood glucose remarkably decreased after supplementation of RJ. In the current study, however, 1000 mg RJ was used
3 times daily. Serum glucose was reduced significantly but HbA1c level was neither significantly different between the two groups, nor before and after the supplementation. In comparison to the placebo group, SBP and IL-6 were significantly reduced after 8 weeks of supplementation (Pourmoradian et al., 2014).
To our knowledge, this is the first randomized controlled trial on RJ supplementation in DM patients. However, the small sample size and short duration of the study can be mentioned as its limitations. Studies with bigger sample size and longer duration are recommended and needed before reaching final conclusions. Further studies are suggested to investigate the effect of RJ on other diseases with inflammatory pathogenesis.
Conclusion
High blood pressure, insulin resistance, and inflammation are the most important risk factors of cardiovascular complications in type 2 diabetic patients. In the present study, supplementation of RJ decreased serum glucose level, SBP, and IL-6. So, RJ may be an effective supplement for decreasing CVDs risk factors in T2DM patients.
Acknowledgements
Authors would like to thank participants, nurses, and physicians of the Firouzgar hospital.
Author’s contribution
Shidfar F and Khoshpay B designed the study. Khoshpay B and Mousavi SN carried out the study. Malek M informed the patients and Hosseini F analyzed the data. Hosseini SH with the biochemical analysis. Mousavi SN and Shidfar F designed the manuscript and all authors studied and approved the final version of the manuscript.
Conflict of interest
Authors declare that there is no conflict of interest.
To the best of our knowledge, this is the first RCT conducted to assess the effects of RJ supplementation on the incidence of cardiovascular risk via measurement of serum glucose, IL-6, HbA1c, and blood pressure in T2DM patients. In this study, intake of RJ significantly reduced serum glucose, SBP, and IL-6 after the intervention but there were no significant differences before and after RJ supplementation in HbA1c and DBP. Some tests were carried out to confirm that RJ reduced the effects of diabetes on animals. The simultaneous administration of RJ and a fructose solution for 8 weeks to insulin-resistant rats significantly reduced plasmatic concentration of insulin, triglycerides, and SBP, without affecting the blood levels of glucose or total cholesterol. These results suggest that RJ can be a functional dietary treatment to prevent from insulin resistance associated with developing hypertension in diabetic patients (Nomura et al., 2007, Zamami et al., 2008). One clinical study demonstrated that RJ significantly affects serum glucose levels in healthy participants (Munstedt et al. 2009). It was reported in another study that RJ reduced the index of insulin resistance (HOMA-IR) but did not reduce blood glucose levels in rats (Zamami et al., 2008). In a recent study, researchers showed that RJ increased catalase activity and antioxidant power, while it decreased malondialdehyde levels in the kidney tissue homogenates of streptozotocin induced diabetic rats (Ghanbari et al., 2015). It has also been shown that RJ contains biologically active substances which causes insulin-like activity (Kramer et al., 1982). Elevated blood glucose level contributes to the proteins and lipid glycation, resulting in the formation of advanced glycation end-products (AGEs) (Pickup, 2004). Receptors for AGEs (RAGE) are expressed in many different tissues and cell types, including endothelial cells, vascular smooth muscle cells, and macrophages (Basta et al., 2004) that lead to the intracellular generation of ROS which activates NF-kB (Wendt et al., 2002). Then, the expression of TNF, IL 1, 6, 8, and 18 as well as interferon-γ (IFN-γ) are increased (Wautier et al., 2001). A clinical study suggests that acute hyperglycaemia can result in elevated levels of circulating inflammatory cytokines, in particular TNF-α, IL-6 and IL-18 (Basta et al., 2002). In one study, the anti-inflammatory actions of RJ at a cytokine level were examined. Supernatants of RJ suspensions were added to a culture of mouse peritoneal macrophages stimulated with lipopolysaccharide and IFN-γ. The production of proinflammatory cytokines such as TNF-α, IL-6, and IL-1 were efficiently inhibited in a dose-dependent manner without having cytotoxic effects on macrophages. This suggests that RJ contains factor(s) responsible for the suppression of proinflammatory cytokines secretion.
Researchers named the factor for honey-
bees, RJ-derived anti-inflammatory factor (HBRJ11AIF) and further investigated its molecular aspects. Size fractionation study showed that HBRJ-AIF is composed of substances of low (< 5 kDa) and high (> 30 kDa) molecular weights; the former is a major component. Chromatographic analysis showed that MRJP3 is one candidate for the HBRJ-AIF with high molecular weights. Thus, these results suggest that RJ has anti-inflammatory actions through inhibiting pro-inflammatory cytokine production by activated macrophages (Kohno et al., 2004). One study indicated that Protease N treated RJ (Pro-RJ) and peptides (IY, VY, IVY) from Pro-RJ, inhibited ACE activity and they have an antihypertensive effect in repeated oral administration for 28 days in spontaneously hypertensive rats (Tokunaga et al. 2004). Another study suggested that the trans-2-octenoic acid and the hydroxydecanoic acid from RJ may be responsible for the anti-hypertensive action, with different RJ fractions exercising bigger or smaller effects on the duration of the action (Librowski and Czarnecki, 2000).
Researchers investigated the anti-inflammatory effects of RJ in formalin-induced rat paw edema; they administered 25, 50, and 100 mg/kg, intera-peritoneal of RJ to these rats. The highest anti-inflammatory effect was observed in doses of 50 and 100 mg/kg (Arzi et al., 2015).
In one human study, researchers determined the effects of RJ supplementation on diabetic females. A single dose of 1000 mg RJ was used in this study. Means of fasting blood glucose remarkably decreased after supplementation of RJ. In the current study, however, 1000 mg RJ was used
3 times daily. Serum glucose was reduced significantly but HbA1c level was neither significantly different between the two groups, nor before and after the supplementation. In comparison to the placebo group, SBP and IL-6 were significantly reduced after 8 weeks of supplementation (Pourmoradian et al., 2014).
To our knowledge, this is the first randomized controlled trial on RJ supplementation in DM patients. However, the small sample size and short duration of the study can be mentioned as its limitations. Studies with bigger sample size and longer duration are recommended and needed before reaching final conclusions. Further studies are suggested to investigate the effect of RJ on other diseases with inflammatory pathogenesis.
Conclusion
High blood pressure, insulin resistance, and inflammation are the most important risk factors of cardiovascular complications in type 2 diabetic patients. In the present study, supplementation of RJ decreased serum glucose level, SBP, and IL-6. So, RJ may be an effective supplement for decreasing CVDs risk factors in T2DM patients.
Acknowledgements
Authors would like to thank participants, nurses, and physicians of the Firouzgar hospital.
Author’s contribution
Shidfar F and Khoshpay B designed the study. Khoshpay B and Mousavi SN carried out the study. Malek M informed the patients and Hosseini F analyzed the data. Hosseini SH with the biochemical analysis. Mousavi SN and Shidfar F designed the manuscript and all authors studied and approved the final version of the manuscript.
Conflict of interest
Authors declare that there is no conflict of interest.
References
Arzi A, Olapour S, Yaghooti H & Karampour NS 2015. Effect of Royal Jelly on Formalin Induced-Inflammation in Rat Hind Paw. Jundishapur journal of natural pharmaceutical products. 10 (1). : e22466.
Basta G, et al. 2002. Advanced glycation end products activate endothelium through signal-transduction receptor RAGE. Circulation. 105 (7): 816-822.
Basta G, Schmidt AM & De Caterina R 2004. Advanced glycation end products and vascular inflammation: implications for accelerated atherosclerosis in diabetes. Cardiovascular research. 63 (4): 582-592.
Brownlee M 2005. The pathobiology of diabetic complications. Diabetes. 54 (6): 1615-1625.
Dandona P, Aljada A, Chaudhuri A & Bandyopadhyay A 2003. The potential influence of inflammation and insulin resistance on the pathogenesis and treatment of atherosclerosis-related complications in type 2 diabetes. The Journal of clinical endocrinology & metabolism. 88 (6): 2422-2429.
Garvey WT, et al. 2003. Effects of insulin resistance and type 2 diabetes on lipoprotein subclass particle size and concentration determined by nuclear magnetic resonance. Diabetes. 52 (2): 453-462.
Ghanbari E, Nejati V & Azadbakht M 2015. Protective effect of royal jelly against renal damage in streptozotocin induced diabetic rats. Iranian journal of toxicology. 9 (28): 1258-1263.
Go AS, et al. 2013. Executive summary: heart disease and stroke statistics: 2013 update: a report from the American Heart Association. circulation. 127 (1): 143-146.
Hang G, et al. 2007. Royal jelly supplementation improves lipoprotein metabolism in humans. Journal of nutritional science and vitaminology. 53 (4): 345-348.
Kohno K, et al. 2004. Royal jelly inhibits the production of proinflammatory cytokines by activated macrophages. Bioscience, biotechnology, and biochemistry. 68 (1): 138-145.
Kramer KJ, Childs CN, Spiers RD & Jacobs RM 1982. Purification of insulin-like peptides from insect haemolymph and royal jelly. Insect biochemistry. 12 (1): 91-98.
Laakso M 1999. Hyperglycemia and cardiovascular disease in type 2 diabetes. Diabetes. 48 (5): 937-942.
Librowski T & Czarnecki R 2000. A comparative analysis of Apistimul Crataegi Forte and royal jelly in induced heart arrhythmia. Herba polonica. 46 (3): 145-150.
Maruyama H, Yoshida C, Tokunaga K, Araki Y & Mishima S 2005. The effect of a peptide (Ile-Val-Tyr) derived from royal jelly treated with protease on blood pressure of spontaneously hypertensive rat. Journal of the Japanese society for food science and technology. 52 (10): 491-494.
Münstedt K, Bargello M & Hauenschild A 2009. Royal jelly reduces the serum glucose levels in healthy subjects. Journal of medicinal food. 12 (5): 1170-1172.
Nomura M, Maruo N, Zamami Y, Takatori S & Kawasaki H 2007. Effect of long-term treatment with royal jelly on insulin resistance in Otsuka Long-Evans Tokushima Fatty (OLETF) rats. Journal of the pharmaceutical society of Japan. 127 (11): 1877-1882.
Pickup JC 2004. Inflammation and activated innate immunity in the pathogenesis of type 2 diabetes. Diabetes care. 27 (3): 813-823.
Pourmoradian S, Mahdavi R, Mobasseri M, Faramarzi E & Mobasseri M 2014. Effects of royal jelly supplementation on glycemic control and oxidative stress factors in type 2 diabetic female: a randomized clinical trial. Chinese journal of integrative medicine. 20 (5): 347-352.
Tokunaga K-h, et al. 2004. Antihypertensive effect of peptides from royal jelly in spontaneously hypertensive rats. Biological and pharmaceutical bulletin. 27 (2): 189-192.
Van Gaal LF, Mertens IL & Christophe E 2006. Mechanisms linking obesity with cardiovascular disease. Nature. 444 (7121): 875-880.
Wautier M-P, et al. 2001. Activation of NADPH oxidase by AGE links oxidant stress to altered gene expression via RAGE. American journal of physiology-endocrinology and metabolism. 280 (5): E685-E694.
Wendt T, et al. 2002. Receptor for advanced glycation endproducts (RAGE) and vascular inflammation: insights into the pathogenesis of macrovascular complications in diabetes. Current atherosclerosis reports. 4 (3): 228-237.
Zamami Y, et al. 2008. Royal jelly ameliorates insulin resistance in fructose-drinking rats. Biological and pharmaceutical bulletin. 31 (11): 2103-2107.
Basta G, et al. 2002. Advanced glycation end products activate endothelium through signal-transduction receptor RAGE. Circulation. 105 (7): 816-822.
Basta G, Schmidt AM & De Caterina R 2004. Advanced glycation end products and vascular inflammation: implications for accelerated atherosclerosis in diabetes. Cardiovascular research. 63 (4): 582-592.
Brownlee M 2005. The pathobiology of diabetic complications. Diabetes. 54 (6): 1615-1625.
Dandona P, Aljada A, Chaudhuri A & Bandyopadhyay A 2003. The potential influence of inflammation and insulin resistance on the pathogenesis and treatment of atherosclerosis-related complications in type 2 diabetes. The Journal of clinical endocrinology & metabolism. 88 (6): 2422-2429.
Garvey WT, et al. 2003. Effects of insulin resistance and type 2 diabetes on lipoprotein subclass particle size and concentration determined by nuclear magnetic resonance. Diabetes. 52 (2): 453-462.
Ghanbari E, Nejati V & Azadbakht M 2015. Protective effect of royal jelly against renal damage in streptozotocin induced diabetic rats. Iranian journal of toxicology. 9 (28): 1258-1263.
Go AS, et al. 2013. Executive summary: heart disease and stroke statistics: 2013 update: a report from the American Heart Association. circulation. 127 (1): 143-146.
Hang G, et al. 2007. Royal jelly supplementation improves lipoprotein metabolism in humans. Journal of nutritional science and vitaminology. 53 (4): 345-348.
Kohno K, et al. 2004. Royal jelly inhibits the production of proinflammatory cytokines by activated macrophages. Bioscience, biotechnology, and biochemistry. 68 (1): 138-145.
Kramer KJ, Childs CN, Spiers RD & Jacobs RM 1982. Purification of insulin-like peptides from insect haemolymph and royal jelly. Insect biochemistry. 12 (1): 91-98.
Laakso M 1999. Hyperglycemia and cardiovascular disease in type 2 diabetes. Diabetes. 48 (5): 937-942.
Librowski T & Czarnecki R 2000. A comparative analysis of Apistimul Crataegi Forte and royal jelly in induced heart arrhythmia. Herba polonica. 46 (3): 145-150.
Maruyama H, Yoshida C, Tokunaga K, Araki Y & Mishima S 2005. The effect of a peptide (Ile-Val-Tyr) derived from royal jelly treated with protease on blood pressure of spontaneously hypertensive rat. Journal of the Japanese society for food science and technology. 52 (10): 491-494.
Münstedt K, Bargello M & Hauenschild A 2009. Royal jelly reduces the serum glucose levels in healthy subjects. Journal of medicinal food. 12 (5): 1170-1172.
Nomura M, Maruo N, Zamami Y, Takatori S & Kawasaki H 2007. Effect of long-term treatment with royal jelly on insulin resistance in Otsuka Long-Evans Tokushima Fatty (OLETF) rats. Journal of the pharmaceutical society of Japan. 127 (11): 1877-1882.
Pickup JC 2004. Inflammation and activated innate immunity in the pathogenesis of type 2 diabetes. Diabetes care. 27 (3): 813-823.
Pourmoradian S, Mahdavi R, Mobasseri M, Faramarzi E & Mobasseri M 2014. Effects of royal jelly supplementation on glycemic control and oxidative stress factors in type 2 diabetic female: a randomized clinical trial. Chinese journal of integrative medicine. 20 (5): 347-352.
Tokunaga K-h, et al. 2004. Antihypertensive effect of peptides from royal jelly in spontaneously hypertensive rats. Biological and pharmaceutical bulletin. 27 (2): 189-192.
Van Gaal LF, Mertens IL & Christophe E 2006. Mechanisms linking obesity with cardiovascular disease. Nature. 444 (7121): 875-880.
Wautier M-P, et al. 2001. Activation of NADPH oxidase by AGE links oxidant stress to altered gene expression via RAGE. American journal of physiology-endocrinology and metabolism. 280 (5): E685-E694.
Wendt T, et al. 2002. Receptor for advanced glycation endproducts (RAGE) and vascular inflammation: insights into the pathogenesis of macrovascular complications in diabetes. Current atherosclerosis reports. 4 (3): 228-237.
Zamami Y, et al. 2008. Royal jelly ameliorates insulin resistance in fructose-drinking rats. Biological and pharmaceutical bulletin. 31 (11): 2103-2107.
Type of article: orginal article |
Subject:
public specific
Received: 2017/01/19 | Published: 2017/11/1 | ePublished: 2017/11/1
Received: 2017/01/19 | Published: 2017/11/1 | ePublished: 2017/11/1
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
