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Journal of Circadian Rhythms

Open Access

A tryptophan-rich breakfast and exposure to light with low color temperature at night improve sleep and salivary melatonin level in Japanese students

  • Kai Wada1,
  • Shota Yata2,
  • Osami Akimitsu1,
  • Milada Krejci3,
  • Teruki Noji2,
  • Miyo Nakade4,
  • Hitomi Takeuchi1 and
  • Tetsuo Harada1Email author
Journal of Circadian Rhythms201311:4

https://doi.org/10.1186/1740-3391-11-4

Received: 10 May 2013

Accepted: 13 May 2013

Published: 25 May 2013

Abstract

Background

Epidemiological studies in Japan have documented an association between morning type and a tryptophan-rich breakfast followed by exposure to sunlight in children. The association may be mediated by enhanced melatonin synthesis, which facilitates sleep at night. However, melatonin is inhibited by artificial light levels with high color-temperature common in Japanese homes at night. In this study, we investigated whether a combination of tryptophan-rich breakfast and light with low color-temperature at night could enhance melatonin secretion and encourage earlier sleep times.

Methods

The intervention included having breakfast with protein- and vitamin B6 - rich foods and exposure to sunlight after breakfast plus exposure to incandescent light (low temperature light) at night (October-November, 2010). The participants were 94 members of a university soccer club, who were divided into 3 groups for the intervention (G1: no intervention; G2: asked to have protein-rich foods such as fermented soybeans and vitamin B6-rich foods such as bananas at breakfast and sunlight exposure after breakfast; G3: the same contents as G2 and incandescent light exposure at night). Salivary melatonin was measured around 11:00 p.m. on the day before the beginning, a mid-point and on the day before the last day a mid-point and on the last day of the 1 month intervention.

Results

In G3, there was a significantly positive correlation between total hours the participants spent under incandescent light at night and the frequency of feeling sleepy during the last week (p = 0.034). The salivary melatonin concentration of G3 was significantly higher than that of G1 and G2 in combined salivary samplings at the mid-point and on the day before the last day of the 1 month intervention (p = 0.018), whereas no such significant differences were shown on the day just before the start of the intervention (p = 0.63).

Conclusion

The combined intervention on breakfast, morning sunlight and evening-lighting seems to be effective for students including athletes to keep higher melatonin secretion at night which seems to induce easy onset of the night sleep and higher quality of sleep.

Keywords

Salivary melatoninTryptophanProtein rich breakfastSunlight exposureLighting with low color temperature

Background

Tryptophan is an essential amino acid that can be absorbed exclusively from meals in humans. It is metabolized via 5-hydroxytryptamine (serotonin) to melatonin by a series of 4 enzymes in the pineal body [1, 2]. Serotonin is known as a precursor to melatonin. A lack of serotonin causes depression, panic disorder, obsessive-compulsive disorder, sleep disorders and eating disorders [3] and induces aggression, anxiety/aggression-driven depression, impulsive behavior and suicidal attempts [4, 5]. Serotonin thus has a strong relationship with mental health. In the past two decades, serotonin reuptake inhibitors (SSRIs) have come to be widely used for the treatment of affective disorders including depression, although [6] there are controversies whether SSRIs are effective or not for the treatment of depression in children and adolescents because of the shortage of coincident scientific evidence of SSRIs for young humans.

Exposure to sunlight in the daytime appears to trigger synthesis of serotonin in the pineal body [7]. This action is hypothesized to occur mainly in the morning hours, because the amount of tryptophan consumed with supper has neither significant effects on Morningness-Eveningness (M-E) scores nor an effect on sleep habits, as shown by another study on young Japanese children performed in 2005 [8].

Melatonin is synthesized in the pineal body of the hypothalamic area and secreted at night. Melatonin level in the serum can be well and positively correlated with that in the saliva [912]. Secretion of melatonin exhibits circadian rhythms and is suppressed by bright light at night [13, 14]. Even room lights such as fluorescent lamps can attenuate melatonin excretion duration at night [15]. Evening lighting conditions are also said to affect circadian rhythms [16, 17] and mental health in mice [18]. Tryptophan intake at breakfast is effective for the onset and offset of sleep in young children [19]. Moreover, questionnaire surveys showed that young children exposed to sunlight for more than 30 minutes after having sources of protein at breakfast are more morning-typed than those exposed for less than 30 minutes [20], and that the more young children take in vitamin B6 at breakfast, the more they exhibit morning typology [21].

Although these findings imply that morning tryptophan and vitamin B6 intake and following exposure to sunlight would promote synthesis of serotonin in the daytime and further to melatonin at night, it is difficult to test the hypothesis only with questionnaire studies. Moreover, this melatonin synthesis might be inhibited by exposure to short-wave (blue) light including light emitted from fluorescent lamps. This hypothesis cannot be tested by questionnaire work and would require an intervention field experiment. An intervention field experiment for was thus performed on university students to test the hypotheses.

Methods

The intervention program was administered to 94 subjects (male, 19-22 years old, average age: 20.33) belonging to a university soccer club. 63 subjects answered to the integrated questionnaire before the intervention period. They were divided into three groups (G1, n = 20: no intervention; G2, n = 22: asked to have protein-rich foods such as fermented soybeans and vitamin B6-rich foods such as bananas at breakfast and sunlight exposure after breakfast; G3, n = 21: the same contents as G2 and incandescent light exposure at night). This university football club includes only men. All the members used fluorescent lamps (white light) for the lighting at night. To estimate the effects of the one month interventions, integrated questionnaires were administered to all participants three times: before the start of the intervention period, immediately after the end of the intervention period, and one month after the end of the intervention period (See note on Figure  1). The questionnaires which were administered before the intervention and 1 month after the intervention consisted of the diurnal-type scale constructed by Torsvall and Åkerstedt [22], questions on sleep habits and meal habits [23], an irritation index, the General Health Questionnaire (GHQ), the Sense of Coherence (SOC) questionnaire, and FFQ (Food Frequency Questionnaire). The questionnaire just after the intervention period of 1 month consisted of self-assessment questions asking how many days during the month-long intervention period they followed the recommendations for breakfast content (the first point), sunlight exposure after breakfast (the second point) and the use of light bulbs that emit lower color temperature light at night (the third point). We made nine groups initially based on the scores of the diurnal-type scale (three groups: morning-type, middle-type, evening-type) and FFQ three groups: good, mid, bad). After that we divided participants into three groups for each of the nine groups with random number list arbitrarily. There were no significant differences among the body height, body mass and age of the three groups.
Figure 1

The schedules of the interventions.

All participants were asked to keep a sleep diary throughout the 30 days of the intervention period, which was October-November in 2010. The sleep diary involved the question, “How was the depth of your last night’s sleep?” to which participants answered every morning. The choices for answer were “deep”, “relatively deep”, “relatively shallow” and “shallow”.

Incandescent light bulbs were distributed one by one to the participants in the G3 group, and these participants were asked to install the light bulb in the room in which they slept at night. The G1 and G2 members were asked to switch fluorescent lamps on and the G3 ones were asked to switch incandescent light bulbs on, instead, when they got back to their residences after sunset. After the incandescent light was set, illumination intensity was measured (Table  1). Participants of G2 and G3 were asked to report their breakfast contents, and G3 were also asked to answer the duration of their time spent under incandescent light each day. 63 of 94 (67%) participants answered the first questionnaire and 51 of 63 (81%) kept sleep diaries for 1 month.
Table 1

Illumination value (Lux) of all subjects in the third group (G3)

 

Standing under the light*

Sitting as usual#

 

Fluorescent

Incandescent

Fluorescent

Incandescent

 

Max

Min.

Ave

Max

Min

Ave

Max

Min

Ave

Max

Min

Ave

A

579

571

574

76

74

74

173

158

166

27

25

26

B

845

601

774

42

38

40

143

122

130

30

18

24

C

186

160

170

18

18

18

34

32

33

9

9

9

D

358

344

352

21

15

18

108

100

105

23

9

18

E

1120

1050

1019

32

28

30

89

86

87

18

15

17

F

1042

1013

1025

42

38

40

272

246

257

5

5

5

G

644

572

604

52

50

51

168

103

144

21

19

19

H

3997

2479

2942

70

61

63

284

277

281

39

38

38

I

1200

1002

1106

24

23

23

205

122

163

7

8

7

J

1155

1106

1132

41

41

41

196

184

189

8

6

6

K

657

651

654

72

70

70

65

64

64

20

18

20

L

173

137

148

26

8

19

134

128

130

18

9

18

M

1092

908

1025

377

360

370

597

263

341

50

37

50

N

   

64

59

61

1

  

131

114

131

O

505

433

465

160

133

150

231

145

86

39

9

39

P

1307

1193

1264

438

431

434

42

41

41

45

45

45

Q

591

542

572

140

129

136

149

146

147

24

20

24

R

1376

1078

1213

544

483

511

66

49

52

9

8

9

S

1

0

1

346

254

316

1

1

1

24

19

24

T

31

30

30

207

193

202

65

58

61

29

23

29

The surface of illumination meter sensor was put vertically just in front of eyes of participants who are standing* or sitting# and illumination value was measured.

The implementation score was calculated from the sum of days that had “high protein content breakfast” and “exposure to >30 min-exposure to sunlight”. For night exposure to low temperature light, the implemental score was defined as the mean hours (per night for 30 days) when participants were exposed to the low temperature light emitted from the incandescent bulb. After the intervention period for 30 days, the participants were asked to mark the scores on “To what extent do you satisfy on your own carrying out each of the two (G2) or three (G3) contents of intervention as a whole for 30 days, marking as 0-100 points as ‘satisfaction score’ ?” (Table  2).
Table 2

Estimates of the extent to which subjects in groups G2 and G3 carried out the intervention

Question: On a scale of 0 to 100, how would you estimate your confidence in your response? The question is “To what extent did you carry out this intervention program during this one month intervention period?

1. Estimate for the whole protocol. (G2, G3)

score /100

2. Estimate for “taking protein-rich and Vitamin B6-rich foods at breakfast”. (G2, G3)

score /100

3. Estimate for “exposure to sunlight after the breakfast”. (G2, G3)

score /100

4. Estimate for “exposure to low color temperature light emitted from incandescent bulbs at night". (G3)

score /100

The salivary melatonin was measured of 10 subjects which were randomly selected from each group because of financial limitation for the chemical analysis (30 participants in total) three times: the day before the start of intervention, at the mid-point (two weeks past in the intervention) and the day before the last day of the intervention. Participants were asked to extract their own saliva at around 23:00 and keep it in a freezer. They turned off the lights when they went to bed (ranging from 23:00 to 2:00).

The saliva samples were collected around 23:00 with cylindrical cotton (1 cm diameter, 3 cm long) which was put under the tongue for 3 min. The saliva samples were kept frozen at −25°C until analysis for 1 or 2 weeks. After centrifugation (1000 × g for 5 min), melatonin concentrations in the saliva samples were determined using an ELISA kit (Direct Saliva Melatonin ELISA, Bulmann, Switzerland).

For the statistical analysis, the “implementation rate” was defined as how many days participants had a protein-rich food (1 point) and Vitamin B6-rich food (1 point) at breakfast and, further, exposed to sunlight for more than 30 min after breakfast (1 point). Participants reported how many minutes they were exposed to low-color temperature lights during the 30 intervention days. The 30-day-long intervention period was divided into 3 parts (FWP: First week period, MP: Medium period of 16 days, LWP: Last week period). The “high implementation group” was defined as 50% participants who marked higher implementation rate in both breakfast contents and exposure to sunlight after breakfast (G2 and G3) and also were exposed to longer hours when they were exposed to the low temperature lights each night (G3). The other 50% participants group was defined as “the low implementation group”.

The software used for statistical analysis was SPSS 12.0 J for Windows (SPSS Inc., Chicago, IL, USA). χ2-test was used for categorized variables and Mann-Whitney U-tests was used for ranked variables. Pearson’s correlation analysis was performed to test the relationship between two numerical variables.

Before the beginning of the study, participants received a full explanation with the code of the guideline for a study targeting humans [24], including that the results of the study would be used only for academic purposes, and all participants completely agreed to participate in the study.

Results

Sleep diary data and salivary melatonin concentration during the 30 days of the intervention

There was significant positive correlation between hours spent under incandescent light at night and the feeling of sleeping well in Last Week Period (LWP) (Pearson’s correlation test: r2 = 0.265, p = 0.034) (Figure  2).
Figure 2

Positive correlation between hours when subjects were exposed to incandescent light at night and the index of feeling of sleeping well in Last Week Period. Upper and lower lines of linear regression line show 95% confidence estimate.

The concentration of salivary melatonin shown by the participants of G3 was significantly higher than that of G1 and G2 in the mid-point and the day before the last day of the intervention (Bonferroni multiple comparison test: G1 versus G3, p = 0.018; G2 versus G3, p = 0.011), whereas there were no significant differences among the three groups on the day just before the start of the intervention (Kruskal Wallis test: χ2-value = 0.92, df = 2, p = 0.63) (Figure  3).
Figure 3

Comparison of salivary melatonin concentration among the three groups. Group 1: no intervention; Group 2: Recommendation of high protein breakfast and exposure to sunlight; Group 3: Same as Group 2 plus the recommendation of exposure to low color temperature light emitted from an incandescent light bulb. A: Melatonin level in the saliva collected on the day just before the intervention (Kruskal Wallis test: χ2-value = 0.92, df = 2, p = 0.63); B: Melatonin in the saliva collected at the mid-point and on the day before the last day of the intervention (Bonferroni multiple comparison test: G1 versus G3, p = 0.018; G2 versus G3, p = 0.011).

The “high implementation group” tended to show a higher concentration of salivary melatonin in MP than the “low implementation group” did in G3 (Mann-Whitney U-test: z = -2.000, p = 0.071) (Figure  4). Participants of G3 tended to follow the morning intervention recommendations (high protein breakfast and sunlight exposure) on more days than G2 participants did (Mann-Whitney U-test: FWP; z = -1.952, p = 0.053, MP; z = -1.628, p = 0.105, LWP; z = 1.253, p = 0.221) (Figure  5). The implementation rate in FWP tended to be higher than in MP (Wilcoxon’s signed rank sum test,: G2:, z = -1.851, p = 0.064; G3:, z = -1.914, p = 0.056) and LWP (G2:, z = -2.298, p = 0.022; G3:, z = -2.898, p = 0.004). The implementation rate in MP tended to be also higher than in LWP in G2 and G3 (G2:, z = -1.681, p = 0.093; G3:, z = -2.533, p = 0.011).
Figure 4

Comparison of melatonin level between “high implementation group” and “low implementation group” of G3 participants. See the text for details.

Figure 5

Comparison of how many days students followed the recommendations during the 30-day-long intervention between two groups in the first week period (FWP), medium period of 2 weeks (MP) and the last week period (LWP).

Several parameters before and after the intervention period

There was a significantly positive correlation between the implementation satisfaction index (Maximum score: 100, Table  2) and the regularity of time to take breakfast and supper (Kendall tau-b test: breakfast, r = 0.058, p = 0.038; supper, r2 = 0.057 p = 0.036).

There was a significant positive correlation between the index of how many days among the 30 days subjects were satisfied in their own implementation of the intervention (of having a breakfast that includes high protein foods) and M-E scores one month after the intervention (higher scores showing morning-type) (Pearson’s correlation test: r2 = 0.195, p = 0.006) (Figure  6).
Figure 6

Positive correlation between M-E scores and the index of satisfaction on the implementation of the intervention on breakfast with high protein foods. Upper and lower lines of linear regression line show 95% confidence estimate.

There was a significant positive correlation between the number of nights when participants were exposed to incandescent light during the month-long intervention and the regularity index of meal time, not only for breakfast, but also for lunch and supper, just after the intervention (Kendall tau b-test: r = -0.574, p = 0.007, r2 = 0.146, p = 0.084, r2 = 0.215, p = 0.029). Participants who ate breakfast more frequently for one month after the intervention showed a lower frequency of having late night snacks during that month (Kendall tau-b test: r2 = -0.142, p = 0.003) than those who ate breakfast less frequently.

The participants in G3 after the intervention showed a lower anger/irritation index than before the intervention (Wilcoxon’s signed rank sum test: z = -3.072, p = 0.002), whereas there was only the tendency towards reduced irritation in G1 (z = -1.786, p = 0.074) and no differences were seen in G2 (z = -0.954, p = 0.340) (Figure  7). Two components of the anger/irritation index, the frequency to be irritated and the frequency to become angry due to small trigger, were also reduced after the intervention in comparison with before the intervention in G3 (Wilcoxon’s signed rank sum test: irritation, z = -2.496, p = 0.013; anger;, z = 2.714, p = 0.007).
Figure 7

Comparison of the anger/irritation index before and after the intervention.

Discussion

This study showed that a triple intervention concerning breakfast content, sunlight exposure after breakfast and exposure to low temperature light emitted from incandescent bulbs is a powerful method for inducing secretion of high amounts of melatonin by the pineal gland in human adults. Underlying mechanisms can be hypothesized to consist of two components. The first is that serotonin synthesis from tryptophan taken at breakfast may be enhanced by the exposure to sunlight just after taking breakfast. The second is that the high potential of melatonin synthesis based on the high serotonin synthesis in the pineal during daytime might be available due to the night exposure to the “low temperature light” emitted from incandescent bulbs. Although many reports have shown that melatonin secretion is suppressed by light emitted from fluorescent lamps including short wave length (with around 460 nm of wave length) components [2527], and especially short wave length light [2730], this study newly implies that the combined behaviors of modifying breakfast content, receiving sunlight exposure and receiving exposure to low color temperature lighting at night can facilitate achievement of high plasma melatonin at night in humans.

Melatonin, a hormone secreted from the pineal gland, causes the core body temperature to decrease and induces sleep [3133]. High plasma melatonin levels at night may play an important role in sleep onset and sleep quality [34]. In this study, the longer time participants spent under incandescent lights at night, the significantly higher scores they marked to feel deep sleep. This better sleep quality might be due to high plasma melatonin levels.

This intervention study supports the hypothesis that the triple intervention of having sources of tryptophan and vitamin B6 at breakfast, following up breakfast with exposure to sunlight and the exposure to low temperature lights as night lighting can stimulate the synthesis of serotonin and succeeding melatonin synthesis at night and that these hormones work as natural anti-depression drugs and/or natural sleeping pills and make students more-morning typed and improve their mental health.

A limitation of this study as a “field intervention experiment” is that we did not include a control group with low-tryptophan breakfast, sunlight exposure, and exposure to low temperature light to find out the importance of the intake of tryptophan at breakfast for the mechanism of tryptophan-serotonin-melatonin pathway more clearly. This study was not a “physiological experiment” to set up several experimental groups and control all the environmental conditions, and such experiment remains to be conducted in the future. Another limitation of this study is that it was performed only with men, whereas the inclusion of participants from a female sports club could add important data on gender differences in response to breakfast modulation and the change in lighting at night.

Consent

Written informed consent was obtained from the participants for publication of this report and any accompanying images.

Declarations

Acknowledgement

We would like to sincerely thank all participants and all staff who supported this epidemiological study. This study was financially supported by Academic Supporting Award by President of Kochi University (2009-2012: To T. Harada), Academic Supporting Award by Dean of Faculty of Education, Kochi University (2008-2009: To T. Harada) and awards from the Japan Society for the Promotion of Science (Award No. 22370089: To T. Harada, Award No. 23-10971 to K. Wada) (2011-2014).

Authors’ Affiliations

(1)
Laboratory of Environmental Physiology, Graduate School of Integrated Arts and Sciences, Kochi University
(2)
Department of Health and Physical Education, Faculty of Education, Kochi University
(3)
Department of Health Education, Faculty of Education, University of South Bohemia
(4)
Department of Nutritional Education, Tokai Gakuen University

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© Wada et al.; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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