Wed, Nov 27, 2024
[Archive]
Volume 7, Issue 2 (May 2022)
JNFS 2022, 7(2): 181-188 |
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:
Ghaem Far Z, Babajafari S, Kojuri J, Nouri M, Ashrafi-Dehkordi E, Mazloomi S M. The Effect of Spirulina on Anxiety in Patients with Hypertension: A Randomized Triple-Blind Placebo-Controlled Clinical Trial. JNFS 2022; 7 (2) :181-188
URL: http://jnfs.ssu.ac.ir/article-1-405-en.html
URL: http://jnfs.ssu.ac.ir/article-1-405-en.html
Zohreh Ghaem Far 
, Siavash Babajafari * , Javad Kojuri , Mehran Nouri , Elham Ashrafi-Dehkordi , Seyed Mohammad Mazloomi
, Siavash Babajafari * , Javad Kojuri , Mehran Nouri , Elham Ashrafi-Dehkordi , Seyed Mohammad Mazloomi
Nutrition Research Center, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
Full-Text [PDF 632 kb]
(630 Downloads)
| Abstract (HTML) (1878 Views)
Full-Text: (558 Views)
The Effect of Spirulina on Anxiety in Patients with Hypertension: A Randomized Triple-Blind Placebo-Controlled Clinical Trial
Zohreh Ghaem Far; MSc 1, Siavash Babajafari; MD, PhD *2, Javad Kojuri; PhD 3, Mehran Nouri; PhD ⁴,⁵,
Elham Ashrafi-Dehkordi; PhD ⁶ & Seyed Mohammad Mazloomi; PhD 2,6
Zohreh Ghaem Far; MSc 1, Siavash Babajafari; MD, PhD *2, Javad Kojuri; PhD 3, Mehran Nouri; PhD ⁴,⁵,
Elham Ashrafi-Dehkordi; PhD ⁶ & Seyed Mohammad Mazloomi; PhD 2,6
1 Department of Clinical Nutrition, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
2 Nutrition Research Center, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
3 Department of Cardiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
4 Department of Community Nutrition, School of Nutrition and Food Science, Shiraz University of Medical Sciences, Shiraz, Iran.
5 Students’ Research Committee, School of Nutrition and Food Science, Shiraz University of Medical Sciences, Shiraz, Iran.
6 Department of Food Hygiene and Quality Control, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
2 Nutrition Research Center, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
3 Department of Cardiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
4 Department of Community Nutrition, School of Nutrition and Food Science, Shiraz University of Medical Sciences, Shiraz, Iran.
5 Students’ Research Committee, School of Nutrition and Food Science, Shiraz University of Medical Sciences, Shiraz, Iran.
6 Department of Food Hygiene and Quality Control, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
| ARTICLE INFO | ABSTRACT | |
| ORIGINAL ARTICLE | Background: High blood pressure, coronary heart disease (CHD), and anxiety ailments entirely lead to many illness in patients and impose expenses on the health care system. Anxiety can significantly predict future CHD consequences. Spirulina is a known antioxidant that has a role in anxiety. The hypothesis was that Spirulina could alleviate anxiety and positively affect hypertension and its consequences. Nonetheless, there are scarce recently developed investigations on assessing the effect of consuming Spirulina on anxiety in human beings. Methods: The present study assessed the effect of Spirulina on anxiety in 48 Iranian patients with hypertension (female and male) aged 24–65 years in a randomized triple-blind, placebo-controlled clinical trial. The patients were given either 2 g Spirulina in the form of spirulina-fortified dressing or placebo. Anxiety levels were evaluated for each patient before and after eight weeks following consumption products with the Beck Anxiety Inventory. Results: Forty-one participants completed the intervention. At the baseline, there was no significant difference in anxiety levels between groups, and they also had the same levels of stress based on the Holmes-Rahe questionnaire. The results showed no significant difference in the level of anxiety between groups after the intervention (P = 0.93). Conclusion: Although no positive results were seen in this study, this novel issue has a potential for further investigations to make comprehensive decisions. Keywords: Spirulina; Anxiety; Beck anxiety inventory; Hypertension |
|
| Article history: Received: 8 May 2021 Revised: 24 Jul 2021 Accepted: 25 Sep 2021 |
||
| *Corresponding author jafaris@sums.ac.ir Head of Nutrition Research Center, School of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran. Postal code: 7153675541 Tel: +98 71-37251001 |
||
| IRCT.ir Identifier: IRCT20200404046940N1 |
A variety of psychosocial parameters involved in cardiovascular disease have been focused for a long time (Player and Peterson, 2011). Anxiety is a negatively perceived emotion as both psychological and somatic features. Psychological indications include worry, tension, and feelings of apprehension, and somatic indications usually arise from autonomic arousal (sweating, palpitations, chest pain, trembling) (Tyrer and Baldwin, 2006). The hypotheses and studies on the relationships between hypertension, CHD, and anxiety ailments have been investigated for long years. Specifically, psychosocial stress inducers accompanying anxiety ailments induce autonomic arousal through the hypothalamic-pituitary axis, thereby increasing catecholamines in the circulation. Longitudinally conducted investigations denote the risky increase in developing high blood pressure in patients suffering from anxiety (Player and Peterson, 2011).
A study by Masood (Masood et al., 2008) indicated that induced oxidative stress (OS) in the hypothalamus and amygdala occurred in accompaniment by anxiety in mice. Research on humans has also revealed the relationship between total oxidant/antioxidant concentrations and anxiety ailments in children and adolescents (Guney et al., 2014). A positive correlation has been observed between an increase in anxiety and rises of reactive oxygen species (ROS) in granulocytes (Bouayed et al., 2007). Investigators have been persuaded by the fallouts of drugs consumed for anxiety therapy and have investigated alternate medication with less unwanted consequences (Cui et al., 2013).
Spirulina, also known as athrospira, is a microscopic and filamentary cyanobacterial species that have historically been used for nutrition for a prolonged time. Spirulina consists of 50-70% protein by weight and is a plentiful resource of vitamins, particularly vitamin B12, β-carotene (provitamin A), and vitamin E. Moreover, it consists of carbohydrates, such as rhamnose, fructose, ribose, mannose, and some minerals, including Cu, Mg, zinc, K, and Fe (Soltani et al., 2012). Spirulina platensis also contains phycobilisomes which are light-collecting protein-pigment complexes. Phycobilisomes include 80-85% of brightly colored polypeptides called phycobiliproteins. Phycocyanin, allophycocyanin, and phycoerythrin with the same chromophoric group are the major biliproteins in these microalgae (Sachin et al., 2014). Spirulina has protective effects against OS, and C-phycocyanin, an active ingredient of Spirulina, which has significant antioxidant properties, contributes to these effects (Romay et al., 2003). Thus, high blood pressure might be controlled by antioxidants which act on anxiety levels. Therefore, regarding the limitations of studies associated with the effects of Spirulina on anxiety, the present study aims to evaluate the anti-anxiety activity of Spirulina Platensis in patients with hypertension.
Materials and Methods
Study design and Participants: Forty eight patients with hypertension were enrolled in this randomized triple-blind placebo-controlled clinical trial. This study was performed at Professor Kojuri clinic, Shiraz, Iran, between January 2020 and March 2020. The inclusion criteria were having systolic blood pressure (SBP) > 130 mm Hg or diastolic blood pressure (DBP) > 80 mm Hg or both of them and age between 24-65 years. The exclusion criteria were history of cardiovascular diseases or cardiac surgery, kidney, liver, inflammatory bowel disease, thyroid disorders, diabetes, and cancer, using any supplements, and following any diet. The detailed information on method and participants properties have been previously published (Ghaem Far et al., 2021)
Intervention: The intervention group (IG, n = 24) received a sachet of salad dressing containing 2 g Spirulina (in the form of spray dried powder purchased from Green Sea Company), and the placebo group (PG, n = 24) received a sachet of salad dressing once a day for eight weeks. All products were produced in Namakin Company with the same formula (with limitation of fat, sugar, salt, and calories), confirming the quality of the products by a health care professional and quality control specialist. For blinding, the study shape and prescription of the sachets were similar in both groups.
Ethical consideration: All patients were fully informed of the study protocols and were free to leave the study at any time. Informed consent
was obtained from all of them who wanted to participate in this study. The study was approved by the Ethics Committee of Shiraz University
of Medical Sciences (Registration number: 1398. 1193) and registered at the IRCT Center (https://en.irct.ir/trial/47011) with the number: IRCT20200404046940N1.
Psychological evaluation: Given the fact that anxiety and stress would contribute to the level of blood pressure, the Beck Anxiety Inventory (BAI) (Beck et al., 1988) and the Holmes–Rahe stress scale (Rahe et al., 1970) were used for assessing the symptoms of anxiety and evaluating the level of stress in groups, respectively. The Holmes-Rahe Stress Questionnaire was completed at the beginning of the study, and BIA was completed twice at the beginning and end of the study by all the patients.
Dietary intake and physical activity assessment: The assessment of the dietary intake, including energy, carbohydrate, protein, fat, Na, K, Ca, and Mg was performed by dietary intake interviews (24-hour recall) at the beginning and end of the trial, and each assessment was included 3 days (2 weekdays and one weekend). The data of the dietary intake were analyzed by the Nutritionist IV software. The physical activity was also assessed using the metabolic equivalent of the task questionnaire (Ainsworth et al., 2000) at the baseline and week 8.
Data analysis: All analyses were conducted using the Statistical Package for the Social Sciences (SPSS) software version 21 (SPSS Inc. Chicago, IL). The results were shown as mean ±SD. Shapiro-Wilk test was used to test the normal distribution in each group. Descriptive statistics, independent t-test, and paired sample t-test were used to analyze continuous quantitative variables. Mann-Whitney and Chi-square tests were used to analyze nominal and ordinal qualitative variables. In all statistical tests, P < 0.05 was considered significant.
Results
From 48 participants included in the study, 41 patients were sampled at the end of the study (Figure 1). The baseline characteristics in Table 1, shows that mean age was not significant among IG and PG (51.27 ± 1.30 vs. 50.21 ± 1.36; P = 0.54). The use of antihypertensive medications in the IG was higher than the PG, but differences were not significant (P = 0.08). The majority of participants in the IG and PG had high school, bachelor, and higher degrees (90.90% vs. 78.95%, P = 0.54). Physical activity changes between the two groups were not significant at baseline and end of the study (P = 0.74, P = 0.21).
The mean dietary intake was not significantly different between the two groups, except for fat at the end. Within-group analysis showed an increase in energy, protein, fat, sodium, and magnesium intake and a decrease in carbohydrate, potassium, and calcium in IG at the end of the study, but differences were not significant
(Table 2).
The results of the Holmes-Rahe questionnaire showed that the patients in both groups were the same in terms of susceptibility to stress-induced health breakdown score, and the distribution of each group was normal (P = 1.00, Table 3).
At baseline, there was no statistically significant difference in the level of anxiety between groups based on BIA (P = 0.05). After the intervention, the change in percentages of the anxiety levels was not shown in the IG, but it was shown in the PG. However, the analyses showed that anxiety levels were not significantly different between the two groups at the end (P = 0.93, Table 3).
A study by Masood (Masood et al., 2008) indicated that induced oxidative stress (OS) in the hypothalamus and amygdala occurred in accompaniment by anxiety in mice. Research on humans has also revealed the relationship between total oxidant/antioxidant concentrations and anxiety ailments in children and adolescents (Guney et al., 2014). A positive correlation has been observed between an increase in anxiety and rises of reactive oxygen species (ROS) in granulocytes (Bouayed et al., 2007). Investigators have been persuaded by the fallouts of drugs consumed for anxiety therapy and have investigated alternate medication with less unwanted consequences (Cui et al., 2013).
Spirulina, also known as athrospira, is a microscopic and filamentary cyanobacterial species that have historically been used for nutrition for a prolonged time. Spirulina consists of 50-70% protein by weight and is a plentiful resource of vitamins, particularly vitamin B12, β-carotene (provitamin A), and vitamin E. Moreover, it consists of carbohydrates, such as rhamnose, fructose, ribose, mannose, and some minerals, including Cu, Mg, zinc, K, and Fe (Soltani et al., 2012). Spirulina platensis also contains phycobilisomes which are light-collecting protein-pigment complexes. Phycobilisomes include 80-85% of brightly colored polypeptides called phycobiliproteins. Phycocyanin, allophycocyanin, and phycoerythrin with the same chromophoric group are the major biliproteins in these microalgae (Sachin et al., 2014). Spirulina has protective effects against OS, and C-phycocyanin, an active ingredient of Spirulina, which has significant antioxidant properties, contributes to these effects (Romay et al., 2003). Thus, high blood pressure might be controlled by antioxidants which act on anxiety levels. Therefore, regarding the limitations of studies associated with the effects of Spirulina on anxiety, the present study aims to evaluate the anti-anxiety activity of Spirulina Platensis in patients with hypertension.
Materials and Methods
Study design and Participants: Forty eight patients with hypertension were enrolled in this randomized triple-blind placebo-controlled clinical trial. This study was performed at Professor Kojuri clinic, Shiraz, Iran, between January 2020 and March 2020. The inclusion criteria were having systolic blood pressure (SBP) > 130 mm Hg or diastolic blood pressure (DBP) > 80 mm Hg or both of them and age between 24-65 years. The exclusion criteria were history of cardiovascular diseases or cardiac surgery, kidney, liver, inflammatory bowel disease, thyroid disorders, diabetes, and cancer, using any supplements, and following any diet. The detailed information on method and participants properties have been previously published (Ghaem Far et al., 2021)
Intervention: The intervention group (IG, n = 24) received a sachet of salad dressing containing 2 g Spirulina (in the form of spray dried powder purchased from Green Sea Company), and the placebo group (PG, n = 24) received a sachet of salad dressing once a day for eight weeks. All products were produced in Namakin Company with the same formula (with limitation of fat, sugar, salt, and calories), confirming the quality of the products by a health care professional and quality control specialist. For blinding, the study shape and prescription of the sachets were similar in both groups.
Ethical consideration: All patients were fully informed of the study protocols and were free to leave the study at any time. Informed consent
was obtained from all of them who wanted to participate in this study. The study was approved by the Ethics Committee of Shiraz University
of Medical Sciences (Registration number: 1398. 1193) and registered at the IRCT Center (https://en.irct.ir/trial/47011) with the number: IRCT20200404046940N1.
Psychological evaluation: Given the fact that anxiety and stress would contribute to the level of blood pressure, the Beck Anxiety Inventory (BAI) (Beck et al., 1988) and the Holmes–Rahe stress scale (Rahe et al., 1970) were used for assessing the symptoms of anxiety and evaluating the level of stress in groups, respectively. The Holmes-Rahe Stress Questionnaire was completed at the beginning of the study, and BIA was completed twice at the beginning and end of the study by all the patients.
Dietary intake and physical activity assessment: The assessment of the dietary intake, including energy, carbohydrate, protein, fat, Na, K, Ca, and Mg was performed by dietary intake interviews (24-hour recall) at the beginning and end of the trial, and each assessment was included 3 days (2 weekdays and one weekend). The data of the dietary intake were analyzed by the Nutritionist IV software. The physical activity was also assessed using the metabolic equivalent of the task questionnaire (Ainsworth et al., 2000) at the baseline and week 8.
Data analysis: All analyses were conducted using the Statistical Package for the Social Sciences (SPSS) software version 21 (SPSS Inc. Chicago, IL). The results were shown as mean ±SD. Shapiro-Wilk test was used to test the normal distribution in each group. Descriptive statistics, independent t-test, and paired sample t-test were used to analyze continuous quantitative variables. Mann-Whitney and Chi-square tests were used to analyze nominal and ordinal qualitative variables. In all statistical tests, P < 0.05 was considered significant.
Results
From 48 participants included in the study, 41 patients were sampled at the end of the study (Figure 1). The baseline characteristics in Table 1, shows that mean age was not significant among IG and PG (51.27 ± 1.30 vs. 50.21 ± 1.36; P = 0.54). The use of antihypertensive medications in the IG was higher than the PG, but differences were not significant (P = 0.08). The majority of participants in the IG and PG had high school, bachelor, and higher degrees (90.90% vs. 78.95%, P = 0.54). Physical activity changes between the two groups were not significant at baseline and end of the study (P = 0.74, P = 0.21).
The mean dietary intake was not significantly different between the two groups, except for fat at the end. Within-group analysis showed an increase in energy, protein, fat, sodium, and magnesium intake and a decrease in carbohydrate, potassium, and calcium in IG at the end of the study, but differences were not significant
(Table 2).
The results of the Holmes-Rahe questionnaire showed that the patients in both groups were the same in terms of susceptibility to stress-induced health breakdown score, and the distribution of each group was normal (P = 1.00, Table 3).
At baseline, there was no statistically significant difference in the level of anxiety between groups based on BIA (P = 0.05). After the intervention, the change in percentages of the anxiety levels was not shown in the IG, but it was shown in the PG. However, the analyses showed that anxiety levels were not significantly different between the two groups at the end (P = 0.93, Table 3).
| Table 1. General characteristics of the participants at baseline and end of the study. | ||||
| Variables | Spirulina group (n=22) | Placebo group (n=19) | P-value | |
| Age (year) | 51.27 ± 1.30c | 50.21 ± 1.36 | 0.54a | |
| Gender Male Female |
11 (50.0)d 11 (50.0) |
8 (42.1) 11 (57.8) |
0.61b | |
| Smoke Yes No |
3 (13.6) 19 (86.4) |
4 (21.1) 15 (78.9) |
0.68 b | |
| Antihypertensive medications Yes No |
21 (95.5) 1 (4.5) |
14 (73.7) 5 (26.3) |
0.08 b | |
| Education Less than high school High school degree Bachelor degree and higher |
2 (9.1) 10 (45.4) 10 (45.4) |
4 (21.0) 8 (42.1) 7 (36.8) |
0.54 b | |
| Physical activity | ||||
| Baseline | Low | 7 (31.8) | 8 (42.1) | 0.74 b |
| Moderate | 6 (27.3) | 4 (21.1) | ||
| High | 6 (27.3) | 3 (15.7) | ||
| Very high | 3 (13.6) | 4 (21.1) | ||
| End | Low | 11 (50.0) | 8 (42.1) | 0.21b |
| Moderate | 6 (27.3) | 2 (10.5) | ||
| High | 4 (18.2) | 4 (21.1) | ||
| Very high | 1 (4.5) | 5 (26.3) | ||
| a: Mann–Whitney U test; b: Fisher’s exact test c: Mean ± SD a; d: N (%). | ||||
| Table 2. Dietary intake of the participants at baseline and end of the study. | |||
| Variables | Spirulina group (n=22) | Placebo group (n=19) | P-value |
| Energy (kcal/day) Baseline End P-valueb |
1609.06 ± 136.38 1572.83 ± 123.41 0.68 |
1571.40 ± 92.78 1655.99 ± 89.92 0.21 |
0.69 a 0.37 |
| Carbohydrate (g/day) Baseline End P-value |
271.35 ± 21.59 257.91 ± 20.26 0.46 |
260.95 ± 18.10 231.71 ± 14.42 0.14 |
1.00 0.33 |
| Protein (g/day) Baseline End P-value |
60.76 ± 6.68 66.02 ± 7.69 0.80 |
57.70 ± 4.98 66.63 ± 6.43 0.27 |
0.81 0.69 |
| Fat (g/day) Baseline End P-value |
36.60 ± 3.76 37.76 ± 3.69 0.91 |
41.37 ± 2.25 55.69 ± 6.00 0.04 |
0.07 0.01 |
| Na (mg/day) Baseline End P-value |
1529.58 ± 140.61 1567.76 ± 136.23 0.75 |
1877.28 ± 177.99 1862.51 ± 190.96 0.87 |
0.15 0.23 |
| K (mg/day) Baseline End P-value |
3329.51 ± 366.72 2954.54 ± 291.78 0.37 |
3372.84 ± 427.31 2703.13 ± 229.51 0.35 |
0.89 0.48 |
| Ca (mg/day) Baseline End P-value |
889.25 ± 133.65 704.62 ± 90.35 0.42 |
854.81 ± 101.07 581.38 ± 60.56 0.01 |
0.54 0.37 |
| Mg (mg/day) Baseline End P-value |
279.18 ± 28.22 289.60 ± 23.09 0.40 |
296.85 ± 31.99 253.78 ± 17.65 0.18 |
0.65 0.34 |
| a: Independent sample t-test; b: Paired sample t-test; c: Mean ± SD. | |||
| Table 3. Results of anxiety and stress levels at baseline and end of the study. | |||
| Variables | Spirulina group (n=22) | Placebo group (n=19) | P-valuea |
| Holmes-Rahe (Baseline) Low Stress Moderate High |
9 (40.9)b 9(40.9) 4 (18.2) |
8 (42.1) 8 (42.1) 3 (15.8) |
1.00 |
| Beck Anxiety Inventory (BAI) | |||
| Baseline | 0.05 |
||
| No Anxiety | 0 (0.0) | 1 (5.3) | |
| Moderate | 13 (59.1) | 5 (26.3) | |
| High | 9 (40.9) | 13 (98.4) | |
| End | 0.93 | ||
| No Anxiety | 0 (0.0) | 0 (0.0) | |
| Moderate | 13 (59.1) | 11 (57.9) | |
| High | 9 (40.9) | 8 (42.1) | |
a: Fisher’s exact test; b: N (%).PNG) |
|||
Discussion
The present study evaluated the effect of Spirulina on anxiety in patients with hypertension. At the end of the study, a significant change in anxiety levels in none of the groups was observed. It is noted that according to the synchronization of the final days of the present study with the start of the COVID-19 pandemic, there is a possibility that the anxiety due to the pandemic affected the results of the study. However, due to the limitations of studies associated with the effects of Spirulina on anxiety, this has a high potential for consideration in future clinical trials.
It has been increasingly evidenced that an imbalance of OS and the antioxidant defensive system may be associated with developing neuropsychiatric disorders, including depression and anxiety. The majority of depression and anxiety are currently associated with a declined overall antioxidant status and by a stimulated OS route. Conventional antidepressants can create therapeutical outcomes different from regulating monoamines by raising the antioxidant concentrations and normalization of the injury induced by OS procedures. There is adequate evidence that antioxidants are capable of removing ROS and reactive nitrogen species (RNS). To this end, they scavenge radicals and suppress the OS route, providing more protection towards neuronal injury induced by oxidative or nitrosative stressors in the brain, expectantly leading to subsidence of depression or anxiety indications. To discover new targets for the therapy of neuropsychiatric disorders, it is necessary to functionally understand the association between OS, depression, and anxiety (Xu et al., 2014).
In an investigation, it was found that supplementing with 500 g/day of vitamin C as an antioxidant for 14 days led to a significant reduction in BAI anxiety scores in high school students (Ribeiro, 2015). Elsewhere, supplementing with 1 g/day of vitamin C for 6 weeks positively affected anxiety levels, depression, and stress compared to 400 IU/day of vitamin E in type-2 diabetic patients. The authors observed significant increases in anxiety scores by the use of vitamin E. They reported that vitamin C could improve anxiety levels by alleviating oxidative injury in the brain, which caused an impaired nervous system (Mazloom et al., 2013). An animal model was used to evaluate the anti-anxiety potentiality of Spirulina platensis in Swiss albino mice, in which the anti-anxiety property improved significantly by a 400 mg/kg dosage of Spirulina platensis (Sachin et al., 2014).
In a study (Moradi et al., 2021) that examined the effect of 8 weeks of spirulina consumption on several parameters, including quality of life in patients with ulcerative colitis, Spirulina caused significant reduction in stress score but the decrease in anxiety, depression or fatigue scores was not significant. The difference between the present study and their study was the dose of Spirulina, which was 2 grams in the present study and 1 gram in their study, but and in terms of anxiety changes, it was in line with the present study.
As reported previously, the chemical composition of Spirulina Platensis is suggestive of the presence of major biliproteins (phycocyanin, allophycocyanin, and phycoerythrin) in Spirulina, acting as a potential antioxidant factor. The mediatory mode of action for the anxiolytic activities of Spirulina is explored by the phycocyanin interplay with the GABAA receptor, possibly modulated by phycocyanin. Nonetheless, the mechanism of action for phycocyanin interplay with the Gamma-aminobutyric acid type A (GABAA) receptor is not known yet. As a result, the action of phycocyanin on anxiety occurs via its antioxidant potentiality (Sachin et al., 2014). A further connection between Spirulina and anxiety may be the amino acids present therein. The nutritious quality of a protein is linked to the quality of amino acids, digestibility coefficient, and its biologic quality. Essential amino acids present in Spirulina are leucine (540 mg per 10g), valine (400mg per 10g), isoleucine (350mg per 10g), and tryptophan (90mg per 10g) (Demelash, 2018).
The synthesis of 5-hydroxytryptamine (5-HT) in the brain is increased by tryptophan, the natural amino acid precursor in 5-HT biosynthesis, thereby possibly stimulating 5‐HT release and function. As a naturally present dietary component, tryptophan must be less toxic and cause little undesirable consequences. Owing to the aforesaid benefits, tryptophan-supplemented diets have been utilized to manage neuropsychiatric disorders, and the outcomes are variably successful (General et al., 2001). Declined brain serotonin (5-HT) concentrations or functioning have been involved in diverse psychopathologic states, including anxiety (Nishizawa et al., 1997). Accordingly, Spirulina is the vital creature in the world, being the paramount and cost-free accessible source that represents the preeminent candidate to enhance the nutritional elements needed for our psychological health (Demelash, 2018).
This study is the first clinical trial to assess the consumption effects of a functional product containing Spirulina on anxiety in patients with hypertension. Out of the weaknesses of the present study, the lack of analysis of OS markers and the activity of antioxidant enzymes were investigated. For a more comprehensive conclusion, it is suggested that future studies use higher dosages, larger sample size, and more duration of intervention.
Conclusion
The results indicate that adding Spirulina as a functional food to salad dressing might be a good option to promote health and reduce the
risk of CVD in hypertensive patients. However, further investigations are required for a more comprehensive conclusion. The authors recommend the implementation of Spirulina in functional food for patients with hypertension in the treatment and prevention methods.
Acknowledgments
The authors would like to thank all the patients for their cooperation in this study. Also, thanks are owed to our colleagues from Green Sea and Namakin Companies that provided Spirulina powder and produced products, respectively, which greatly assisted the research. The present manuscript was extracted from a part of the Master of Sciences thesis written by Zohreh Ghaem Far and was financially supported by Shiraz University of Medical Sciences.
Conflict of interest
The authors declare that there is no conflict of interest.
Authors’ contributions
Ghaem Far Z, Babajafari S and Mazloomi SM participated in propose the original idea of the study, supervise the work. Ghaem Far Z also carried out the stages of intervention, data collection, draft the article, and review. Mazloomi SM also contributed to formulation of the products, investigation of required analytical tests, quality as well as the safety of the products. Nouri N contributed to draft and revision of the article and final approval of the manuscript. Ashrafi-Dehkordi contribute to data analysis, statistical analysis, and interpretation. Kojuri J visited the patients and carry out the stages of intervention. All authors read and approved the final version of the manuscript.
References
Ainsworth BE, et al. 2000. Compendium of physical activities: an update of activity
codes and MET intensities. Medicine and science in sports and exercise. 32 ( SUPP/1): S498-S504.
Beck AT, Epstein N, Brown G & Steer RA 1988. An inventory for measuring clinical anxiety: psychometric properties. Journal of consulting clinical psychology. 56 (6): 893.
Bouayed J, Rammal H, Younos C & Soulimani R 2007. Positive correlation between peripheral blood granulocyte oxidative status and level of anxiety in mice. European journal of pharmacology. 564 (1-3): 146-149.
Cui Y, et al. 2013. Mechanism-based anti-anxiety effects of polysaccharides extracted from shudihuang (radix rehmanniae preparata) by two-dimensional electrophoresis analysis in rat hippocampus proteins. Journal of traditional Chinese medicine. 33 (4): 524-530.
Demelash S 2018. Spirulina as a main source of tryptophan for mental illness: Improving level of serotonin through tryptophan supplementation. Global journal of medicine and public health. 7 (2): 1-5.
General USPHSOotS, Services CfMH, Health NIoM, Abuse USS & Administration MHS 2001. Mental health: Culture, race, and ethnicity: A supplement to mental health: A report of the Surgeon General. Department of Health and Human Services, US Public Health Service.
Ghaem Far Z, et al. 2021. Antihypertensive and antihyperlipemic of spirulina (Arthrospira platensis) sauce on patients with hypertension: A randomized triple‐blind placebo‐controlled clinical trial. Phytotherapy Research. 35: 6181-6190.
Guney E, et al. 2014. Oxidative stress in children and adolescents with anxiety disorders. Journal of affective disorders. 156: 62-66.
Masood A, Nadeem A, Mustafa SJ & O'Donnell JM 2008. Reversal of oxidative stress-induced anxiety by inhibition of phosphodiesterase-2 in mice. Journal of pharmacology experimental therapeutics. 326 (2): 369-379.
Mazloom Z, Ekramzadeh M & Hejazi N 2013. Efficacy of Supplementary Vitamins C and E on Anxiety, Depression and Stress in Type 2 Diabetic Patients: A Randomized, Single-blind, Placebo-controlled Trial. Pakistan journal of biological sciences. 16 (22): 1597-1600.
Moradi S, Zobeiri M, Feizi A, Clark CC & Entezari MH 2021. The Effects of Spirulina (Arthrospira platensis) Supplementation on Anthropometric Indices, Blood Pressure, Sleep Quality, Mental Health, Fatigue Status, and Quality of Life in Patients with Ulcerative Colitis: A Randomized, Double‐blinded, Placebo‐controlled Trial. International journal of clinical practice. 13 (9): 3054.
Nishizawa S, et al. 1997. Differences between males and females in rates of serotonin synthesis in human brain. Proceedings of the national academy of sciences. 94 (10): 5308-5313.
Player MS & Peterson LE 2011. Anxiety disorders, hypertension, and cardiovascular risk: a review. International journal of psychiatry in medicine. 41 (4): 365-377.
Rahe RH, Mahan Jr JL & Arthur R 1970. Prediction of near-future health change from subjects' preceding life changes. Journal of psychosomatic research. 14 (4): 401-406.
Ribeiro C 2015. Effects of oral vitamin C supplementation on anxiety in students: a double-blind, randomized, placebo-controlled trial. Pakistan journal of biological sciences. 18 (1): 11-18.
Romay C, Gonzalez R, Ledon N, Remirez D & Rimbau V 2003. C-phycocyanin: a biliprotein with antioxidant, anti-inflammatory and neuroprotective effects. Current protein peptide science. 4 (3): 207-216.
Sachin N, et al. 2014. Asseessment ofF anxiolytic potential of spirulina platensis. International journal of pharmaceutical sciences and research. 5 (9): 4067-4071.
Soltani M, Khosravi A-R, Asadi F & Shokri H 2012. Evaluation of protective efficacy of Spirulina platensis in Balb/C mice with candidiasis. Journal de mycologie médicale. 22 (4): 329-334.
Tyrer P & Baldwin D 2006. Generalised anxiety disorder. Lancet. 368 (9553): 2156-2166.
Xu Y, Wang C, J Klabnik J & M O'Donnell J 2014. Novel therapeutic targets in depression and anxiety: antioxidants as a candidate treatment. Current neuropharmacology. 12 (2): 108-119.
The present study evaluated the effect of Spirulina on anxiety in patients with hypertension. At the end of the study, a significant change in anxiety levels in none of the groups was observed. It is noted that according to the synchronization of the final days of the present study with the start of the COVID-19 pandemic, there is a possibility that the anxiety due to the pandemic affected the results of the study. However, due to the limitations of studies associated with the effects of Spirulina on anxiety, this has a high potential for consideration in future clinical trials.
It has been increasingly evidenced that an imbalance of OS and the antioxidant defensive system may be associated with developing neuropsychiatric disorders, including depression and anxiety. The majority of depression and anxiety are currently associated with a declined overall antioxidant status and by a stimulated OS route. Conventional antidepressants can create therapeutical outcomes different from regulating monoamines by raising the antioxidant concentrations and normalization of the injury induced by OS procedures. There is adequate evidence that antioxidants are capable of removing ROS and reactive nitrogen species (RNS). To this end, they scavenge radicals and suppress the OS route, providing more protection towards neuronal injury induced by oxidative or nitrosative stressors in the brain, expectantly leading to subsidence of depression or anxiety indications. To discover new targets for the therapy of neuropsychiatric disorders, it is necessary to functionally understand the association between OS, depression, and anxiety (Xu et al., 2014).
In an investigation, it was found that supplementing with 500 g/day of vitamin C as an antioxidant for 14 days led to a significant reduction in BAI anxiety scores in high school students (Ribeiro, 2015). Elsewhere, supplementing with 1 g/day of vitamin C for 6 weeks positively affected anxiety levels, depression, and stress compared to 400 IU/day of vitamin E in type-2 diabetic patients. The authors observed significant increases in anxiety scores by the use of vitamin E. They reported that vitamin C could improve anxiety levels by alleviating oxidative injury in the brain, which caused an impaired nervous system (Mazloom et al., 2013). An animal model was used to evaluate the anti-anxiety potentiality of Spirulina platensis in Swiss albino mice, in which the anti-anxiety property improved significantly by a 400 mg/kg dosage of Spirulina platensis (Sachin et al., 2014).
In a study (Moradi et al., 2021) that examined the effect of 8 weeks of spirulina consumption on several parameters, including quality of life in patients with ulcerative colitis, Spirulina caused significant reduction in stress score but the decrease in anxiety, depression or fatigue scores was not significant. The difference between the present study and their study was the dose of Spirulina, which was 2 grams in the present study and 1 gram in their study, but and in terms of anxiety changes, it was in line with the present study.
As reported previously, the chemical composition of Spirulina Platensis is suggestive of the presence of major biliproteins (phycocyanin, allophycocyanin, and phycoerythrin) in Spirulina, acting as a potential antioxidant factor. The mediatory mode of action for the anxiolytic activities of Spirulina is explored by the phycocyanin interplay with the GABAA receptor, possibly modulated by phycocyanin. Nonetheless, the mechanism of action for phycocyanin interplay with the Gamma-aminobutyric acid type A (GABAA) receptor is not known yet. As a result, the action of phycocyanin on anxiety occurs via its antioxidant potentiality (Sachin et al., 2014). A further connection between Spirulina and anxiety may be the amino acids present therein. The nutritious quality of a protein is linked to the quality of amino acids, digestibility coefficient, and its biologic quality. Essential amino acids present in Spirulina are leucine (540 mg per 10g), valine (400mg per 10g), isoleucine (350mg per 10g), and tryptophan (90mg per 10g) (Demelash, 2018).
The synthesis of 5-hydroxytryptamine (5-HT) in the brain is increased by tryptophan, the natural amino acid precursor in 5-HT biosynthesis, thereby possibly stimulating 5‐HT release and function. As a naturally present dietary component, tryptophan must be less toxic and cause little undesirable consequences. Owing to the aforesaid benefits, tryptophan-supplemented diets have been utilized to manage neuropsychiatric disorders, and the outcomes are variably successful (General et al., 2001). Declined brain serotonin (5-HT) concentrations or functioning have been involved in diverse psychopathologic states, including anxiety (Nishizawa et al., 1997). Accordingly, Spirulina is the vital creature in the world, being the paramount and cost-free accessible source that represents the preeminent candidate to enhance the nutritional elements needed for our psychological health (Demelash, 2018).
This study is the first clinical trial to assess the consumption effects of a functional product containing Spirulina on anxiety in patients with hypertension. Out of the weaknesses of the present study, the lack of analysis of OS markers and the activity of antioxidant enzymes were investigated. For a more comprehensive conclusion, it is suggested that future studies use higher dosages, larger sample size, and more duration of intervention.
Conclusion
The results indicate that adding Spirulina as a functional food to salad dressing might be a good option to promote health and reduce the
risk of CVD in hypertensive patients. However, further investigations are required for a more comprehensive conclusion. The authors recommend the implementation of Spirulina in functional food for patients with hypertension in the treatment and prevention methods.
Acknowledgments
The authors would like to thank all the patients for their cooperation in this study. Also, thanks are owed to our colleagues from Green Sea and Namakin Companies that provided Spirulina powder and produced products, respectively, which greatly assisted the research. The present manuscript was extracted from a part of the Master of Sciences thesis written by Zohreh Ghaem Far and was financially supported by Shiraz University of Medical Sciences.
Conflict of interest
The authors declare that there is no conflict of interest.
Authors’ contributions
Ghaem Far Z, Babajafari S and Mazloomi SM participated in propose the original idea of the study, supervise the work. Ghaem Far Z also carried out the stages of intervention, data collection, draft the article, and review. Mazloomi SM also contributed to formulation of the products, investigation of required analytical tests, quality as well as the safety of the products. Nouri N contributed to draft and revision of the article and final approval of the manuscript. Ashrafi-Dehkordi contribute to data analysis, statistical analysis, and interpretation. Kojuri J visited the patients and carry out the stages of intervention. All authors read and approved the final version of the manuscript.
References
Ainsworth BE, et al. 2000. Compendium of physical activities: an update of activity
codes and MET intensities. Medicine and science in sports and exercise. 32 ( SUPP/1): S498-S504.
Beck AT, Epstein N, Brown G & Steer RA 1988. An inventory for measuring clinical anxiety: psychometric properties. Journal of consulting clinical psychology. 56 (6): 893.
Bouayed J, Rammal H, Younos C & Soulimani R 2007. Positive correlation between peripheral blood granulocyte oxidative status and level of anxiety in mice. European journal of pharmacology. 564 (1-3): 146-149.
Cui Y, et al. 2013. Mechanism-based anti-anxiety effects of polysaccharides extracted from shudihuang (radix rehmanniae preparata) by two-dimensional electrophoresis analysis in rat hippocampus proteins. Journal of traditional Chinese medicine. 33 (4): 524-530.
Demelash S 2018. Spirulina as a main source of tryptophan for mental illness: Improving level of serotonin through tryptophan supplementation. Global journal of medicine and public health. 7 (2): 1-5.
General USPHSOotS, Services CfMH, Health NIoM, Abuse USS & Administration MHS 2001. Mental health: Culture, race, and ethnicity: A supplement to mental health: A report of the Surgeon General. Department of Health and Human Services, US Public Health Service.
Ghaem Far Z, et al. 2021. Antihypertensive and antihyperlipemic of spirulina (Arthrospira platensis) sauce on patients with hypertension: A randomized triple‐blind placebo‐controlled clinical trial. Phytotherapy Research. 35: 6181-6190.
Guney E, et al. 2014. Oxidative stress in children and adolescents with anxiety disorders. Journal of affective disorders. 156: 62-66.
Masood A, Nadeem A, Mustafa SJ & O'Donnell JM 2008. Reversal of oxidative stress-induced anxiety by inhibition of phosphodiesterase-2 in mice. Journal of pharmacology experimental therapeutics. 326 (2): 369-379.
Mazloom Z, Ekramzadeh M & Hejazi N 2013. Efficacy of Supplementary Vitamins C and E on Anxiety, Depression and Stress in Type 2 Diabetic Patients: A Randomized, Single-blind, Placebo-controlled Trial. Pakistan journal of biological sciences. 16 (22): 1597-1600.
Moradi S, Zobeiri M, Feizi A, Clark CC & Entezari MH 2021. The Effects of Spirulina (Arthrospira platensis) Supplementation on Anthropometric Indices, Blood Pressure, Sleep Quality, Mental Health, Fatigue Status, and Quality of Life in Patients with Ulcerative Colitis: A Randomized, Double‐blinded, Placebo‐controlled Trial. International journal of clinical practice. 13 (9): 3054.
Nishizawa S, et al. 1997. Differences between males and females in rates of serotonin synthesis in human brain. Proceedings of the national academy of sciences. 94 (10): 5308-5313.
Player MS & Peterson LE 2011. Anxiety disorders, hypertension, and cardiovascular risk: a review. International journal of psychiatry in medicine. 41 (4): 365-377.
Rahe RH, Mahan Jr JL & Arthur R 1970. Prediction of near-future health change from subjects' preceding life changes. Journal of psychosomatic research. 14 (4): 401-406.
Ribeiro C 2015. Effects of oral vitamin C supplementation on anxiety in students: a double-blind, randomized, placebo-controlled trial. Pakistan journal of biological sciences. 18 (1): 11-18.
Romay C, Gonzalez R, Ledon N, Remirez D & Rimbau V 2003. C-phycocyanin: a biliprotein with antioxidant, anti-inflammatory and neuroprotective effects. Current protein peptide science. 4 (3): 207-216.
Sachin N, et al. 2014. Asseessment ofF anxiolytic potential of spirulina platensis. International journal of pharmaceutical sciences and research. 5 (9): 4067-4071.
Soltani M, Khosravi A-R, Asadi F & Shokri H 2012. Evaluation of protective efficacy of Spirulina platensis in Balb/C mice with candidiasis. Journal de mycologie médicale. 22 (4): 329-334.
Tyrer P & Baldwin D 2006. Generalised anxiety disorder. Lancet. 368 (9553): 2156-2166.
Xu Y, Wang C, J Klabnik J & M O'Donnell J 2014. Novel therapeutic targets in depression and anxiety: antioxidants as a candidate treatment. Current neuropharmacology. 12 (2): 108-119.
Type of article: orginal article |
Subject:
public specific
Received: 2021/05/8 | Published: 2022/05/30 | ePublished: 2022/05/30
Received: 2021/05/8 | Published: 2022/05/30 | ePublished: 2022/05/30
Send email to the article author
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
