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- Green Tea (Camellia sinensis)
- Reward Learning
- Depression
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Date:
08-30-2013 | HC# 081331-479
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Re: Green Tea Intake Improves Reward Learning and Symptoms of Depression
Zhang
Q, Yang H, Wang J, et al. Effect of green tea on reward learning in healthy
individuals: a randomized, double-blind, placebo-controlled pilot study. Nutr J. 2013;12(1):84. doi:
10.1186/1475-2891-12-84.
Green
tea (Camellia sinensis) extracts, as
well as their main component, the polyphenol epigallocatechin-3-gallate (EGCG),
reportedly have antistress, anticancer, and antioxidant effects. Recent studies
suggest a beneficial association between green tea consumption and symptoms of
depression; however, the underlying mechanism behind that association is
unclear. Anhedonia, the inability to experience pleasure, is a characteristic
of depression, marked by reduced pleasure, altered motivation, and disturbed
reward learning.1,2 A reduced reward-learning function has been linked
to persistent anhedonia in depressed patients.3 These authors
hypothesized that chronic treatment with green tea would improve reward
learning compared with a control treatment. They conducted a randomized,
double-blind, placebo-controlled study to evaluate the effects of green tea on
reward learning and the clinical outcome of depression.
Through
local advertisements, the authors recruited 74 healthy subjects aged between 18
and 34 years (mean age = 25.7 ± 4.7 years) for the study, conducted from March
to November 2012 at Shandong University in Shandong, China. Before enrollment,
the subjects underwent thorough screening that included a medical history
interview, physical examination, determination of typical tea consumption
patterns, and clinical laboratory tests. Subjects
were excluded if they drank > 3 cups of tea/day; however, the authors do not
state whether those participating continued to drink less than that amount
during the trial. The Montgomery-Asberg Depression Rating Scale (MADRS)
and a 17-item Hamilton Rating Scale for Depression (HRSD-17) were used to measure
symptoms of depression at baseline and at the end of the trial.
At
baseline, the subjects were similar in age, education, and behavioral phenotype
as assessed by MADRS and HRSD-17 scores. Of the original 74 subjects, 46
completed the study – 22 in the placebo group and 24 in the green tea group.
After
being randomly assigned to either the green tea or placebo treatment, the
subjects were asked to take 1 package containing 400 mg of either green tea
powder (Yifutang Tea Co., Ltd.; Hangzhou, Zhejiang Province, China) or
cellulose (placebo) 3 times daily for 5 weeks. The green tea powder was
dissolved in hot water and consumed 30 minutes after each meal. Composition of
the green tea powder was determined by high-performance liquid chromatography (HPLC)
to be 45.6% EGCG, 16.7% epigallocatechin, 11.4% epicatechin-3-gallate, 6.8%
epicatechin, and 0.6% caffeine.
The
authors explain that a monetary incentive delay (MID) task is used "to
assess the effort-related aspects of central reward processing for investigations
of the relationship between depressive behavior and impairments in reward
learning."4 In this study, the MID task included 30 potential
reward trials, 30 no-reward trials, and 30 periods of fixation. Trials lasted
between 7.5 and 10.5 seconds; the total duration of the task was 13.5 minutes.
Cues signaled potential reward outcomes or no-reward outcomes. The subjects
could win or avoid losing money by pressing a button during target
presentation. If a subject pushed the target in a rewarding trial, he or she earned
1 Yuan. The subjects were told they would receive one-third of the money they
won during the MID in each session at the end of the study.
The
statistical analyses of the reward learning and depressive behavioral data were
performed by using repeated-measure analysis of
variance (ANOVA). For the MID task, ANOVA showed that the green tea
group had a significantly shorter reaction time in response to the reward trial
compared with the placebo group (P<0.01), suggesting that those treated with
green tea exhibited significantly increased reward learning. No differences
were observed in the reaction time in the no-reward trials between the 2
groups. "It has been evidenced that reduced dopamine neurotransmission
might contribute to the anhedonia and loss of behavioral incentive in
depressive disorder, therefore it is important to examine the regulatory role
of green tea on the brain circuitry activated by reward learning," write
the authors.
Furthermore,
the data revealed decreased MADRS (P<0.05) and HRSD-17 (P<0.001) scores
after treatment with green tea compared with baseline values. For those in the
placebo group, the MADRS and HRSD-17 scores did not change significantly during
the trial. Compared with the control treatment, the green tea produced
significantly greater improvements in the MADRS (P<0.01) and HRSD-17
(P<0.001) total scores.
In
earlier studies, green tea and its polyphenol EGCG have exhibited protective
effects against neurodegenerative diseases, including Parkinson's disease and
Alzheimer's disease.
The
findings in this study suggest that the administration of green tea for 5 weeks
was beneficial for reward learning and the improvement of depressive symptoms.
"We propose that green tea would probably have the potential for
normalization of anhedonia through improve[d] reward learning and have
implications for the prevention of depression," conclude the authors. The
authors do not state if there was a washout period
prior to the beginning of the study; whether or not the participants were
allowed to drink green tea other than the test material; and whether or not the
participants were allowed to have other forms of caffeine, such as coffee (Coffea spp.).
―Shari
Henson
References
1Davidson RJ. Affective
neuroscience and psychophysiology: toward a synthesis. Psychophysiology. 2003;40(5):655-665.
2Treadway MT, Zald DH.
Reconsidering anhedonia in depression: lessons from translational neuroscience.
Neurosci Biobehav Rev. 2011;35(3):537-555.
3Hasler G, Fromm S,
Carlson PJ, et al. Neural response to catecholamine depletion in unmedicated
subjects with major depressive disorder in remission and healthy subjects. Arch Gen Psychiatry. 2008;65(5):521-531.
4Knutson B, Adams CM,
Fong GW, Hommer D. Anticipation of increasing monetary reward selectively
recruits nucleus accumbens. J Neurosci.
2001;21(16):RC159.
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