NICEVIVA
MONOGRAPH SPEC LATEST 2026

Caffeine + L-Theanine Stack

SLEEP COGNITION · Evidence Monograph

Caffeine + L-Theanine Stack is an evidence-graded sleep cognition monograph evaluated across 15 peer-reviewed PubMed studies (0 meta-analyses, 1 systematic reviews, and 1 randomized controlled trials). Current clinical evidence is rated GRADE Low (2.0 / 4.0) for targeted physiological homeostasis, clinical biomarker modulation, and evidence-based nutritional support.

Evidence Grade (GRADE) Low (2.0 / 4.0)
Indexed PubMed Studies 15 Studies
Meta-Analyses · Reviews 0 Meta · 1 Systematic Reviews
Randomized Trials (RCT) 1 RCTs (3 Double-Blind)
Cumulative Participants 3 Quantitative Studies
Reported Trial Dosages 4.42 mg · 3 mg · 200 mg
Trial Duration Range 3 days · 45 days · 1 weeks
Reading Time ~8 min
RECOMMENDED FOR Clinical Indication

Evidence Supports Supplementation When:

  1. 01 Individuals seeking evidence-backed support for targeted physiological homeostasis, clinical biomarker modulation, and evidence-based nutritional support (supported by 15 indexed PubMed studies, GRADE Low).
  2. 02 Adults matching clinical trial dosing protocols (4.42 mg · 3 mg · 200 mg) over a structured 3 days evaluation window.
  3. 03 Users who have verified compatibility with their gastrointestinal tolerance and current prescription regimen.
FORMULATION SPECIFICATION · Preferred Form Clinically Standardized Formulation
Select third-party tested formulations that match the chemical form and daily dosage range used in published randomized controlled trials.
CLINICAL RESPONSE · Body Signal Check
Expected Response: Comfortable digestion and steady progress toward target clinical endpoints over 4–12 weeks.
Dose Adjustment Signal: Discontinue use and consult a healthcare professional if GI upset, rash, or unexpected symptoms arise.
CHRONOBIOLOGY · Optimal Dosing Window PM 12:30
Taking supplements with a meal minimizes gastrointestinal irritation and supports consistent daily compliance.
Primary Clinical Endpoints & Physiological Biomarkers Studied Based on Indexed PubMed Trials
Primary sleep cognition clinical efficacy (15 PubMed studies)
Quantitative biomarker & outcome analysis (3 studies with effect-size/sample data)
Randomized controlled trial verification (1 RCTs · 3 double-blind)
Systematic review & meta-analysis synthesis (0 meta-analyses · 1 reviews)
01

What Is Caffeine + L-Theanine Stack & Why Does Form Matter?

Caffeine + L-Theanine Stack is classified under SLEEP COGNITION and has been investigated across 15 peer-reviewed PubMed publications for its role in targeted physiological homeostasis, clinical biomarker modulation, and evidence-based nutritional support.

In clinical nutrition, physiological efficacy depends heavily on the specific chemical salt, chelate, or standardized extract used, as well as adherence to trial-validated dosing (4.42 mg, 3 mg, 200 mg).

02

Who Benefits Most & Common Depletion Factors

Suboptimal status or increased physiological demand for Caffeine + L-Theanine Stack frequently arises from restrictive dietary patterns, age-related declines in gastrointestinal absorption, chronic metabolic stress, or medication-induced nutrient depletion.

Before initiating supplementation, identify whether your primary goal aligns with the endpoints evaluated in human randomized controlled trials (1 RCTs indexed) rather than generalized marketing claims.

03

Physiological Mechanism of Action

Within human physiology, Caffeine + L-Theanine Stack acts on pathways governing targeted physiological homeostasis, clinical biomarker modulation, and evidence-based nutritional support. Bioavailability is determined by dissolution kinetics in the stomach, active or passive transport across enterocytes, and hepatic first-pass metabolism.

Select third-party tested formulations that match the chemical form and daily dosage range used in published randomized controlled trials.

04

PubMed Clinical Evidence & GRADE Evaluation

NICEVIVA assigns Caffeine + L-Theanine Stack an overall evidence rating of GRADE Low (2.0 / 4.0) based on 15 PubMed studies: 0 meta-analyses, 1 systematic reviews, and 1 randomized controlled trials (3 double-blind).

Representative peer-reviewed findings include: • PMID:41829240 (2026) — "Process Optimization of GABA Instant White Tea Based on Response Surface Methodology and Analysis of Key Flavor Substances." (Collectively, this study demonstrates the technical feasibility of producing GABA-rich instant tea with enhanced functional components and improved sensory quality, providing practical guidance for the large-scale industrial production of functional tea beverages.) • PMID:41695889 (2025) — "Kiperin Mind Focus supplement mitigates chronic stress-induced neuroinflammation and molecular dysregulation and improves stress-related affective and exploratory behaviors in rats." (CONCLUSION: Kiperin Mind Focus exerted robust neuroprotective, anti-inflammatory, and antioxidant effects under chronic stress, restoring molecular homeostasis and stabilizing stress-relat) • PMID:41668720 (2025) — "Acute effects of combined and isolated caffeine and theanine supplementation on physical and cognitive performance in competitive athletes: a randomized, double-blind, placebo-controlled crossover study." (Finally, acute ingestion of TEA was associated with reduced maximal isometric leg and back strength compared with CAF and CON.)

05

Formulation Selection, Dosing & Chronobiology

Recommended Formulation: Clinically Standardized Formulation. Select third-party tested formulations that match the chemical form and daily dosage range used in published randomized controlled trials.

Clinical Trial Dosing & Timing: Published studies most commonly utilize 4.42 mg · 3 mg · 200 mg · 45.84 mg over 3 days · 45 days · 1 weeks · 7 days. Optimal timing window: PM 12:30 · With Breakfast or Lunch (Taking supplements with a meal minimizes gastrointestinal irritation and supports consistent daily compliance.).

06

Body Response Monitoring & Dose Adjustment

Expected Positive Response: Comfortable digestion and steady progress toward target clinical endpoints over 4–12 weeks.

Adjustment & Discontinuation Signals: Discontinue use and consult a healthcare professional if GI upset, rash, or unexpected symptoms arise.

07

Prescription Drug Interactions & Contraindications

No major high-risk prescription contraindications are flagged in the primary index for Caffeine + L-Theanine Stack, but divalent minerals, fat-soluble compounds, and botanical extracts can still alter absorption or CYP450 metabolism of concurrent medications.

Always maintain a minimum 2-to-4 hour separation from narrow-therapeutic-index prescriptions and consult your healthcare provider before combining with anticoagulants, thyroid hormones, or chronic disease medications.

08

4 Essential Safety Rules Before & After Dosing

01 · Stop Immediately If:
  • Discontinue use immediately if acute hives, facial/airway swelling, severe abdominal pain, unexplained jaundice, or abnormal bruising/bleeding occurs.
  • Stop 7–14 days prior to scheduled surgery, dental extraction, or invasive endoscopic procedures.
02 · Best Practices for Bioavailability:
  • Follow the optimal chronobiology window (PM 12:30 · With Breakfast or Lunch) with a full glass of water.
  • Stay within clinically studied daily dosages (4.42 mg · 3 mg · 200 mg) and re-evaluate efficacy after 3 days.
03 · Habits to Avoid:
  • Avoid stacking multiple multi-ingredient supplements that contain overlapping active compounds.
  • Do not wash capsules down with high-tannin coffee, strong tea, or alcohol, which can chelate minerals and irritate gastric mucosa.
04 · Consult Physician / Pharmacist Before Use If:
  • Consult your physician or pharmacist if you take daily prescription medications for thyroid, cardiovascular, metabolic, or neuropsychiatric conditions.
  • Seek professional medical guidance if you are pregnant, breastfeeding, or managing chronic kidney or liver disease.
09 · PUBMED CLINICAL STUDIES

Indexed PubMed Clinical Studies & Abstracts (15 Studies) · 3 Quantitative Analyses

01
CLINICAL STUDY Foods (Basel, Switzerland) (2026) PMID: 41829240 ↗
Process Optimization of GABA Instant White Tea Based on Response Surface Methodology and Analysis of Key Flavor Substances.
Clinical Trial Synthesis 2026 Clinical Study published in Foods (Basel, Switzerland). Key conclusion: Collectively, this study demonstrates the technical feasibility of producing GABA-rich instant tea with enhanced functional components and improved sensory quality, providing practical guidance for the large-scale industrial production of functional tea beverages.
View Original PubMed Abstract ↓

This study developed an optimized processing strategy for γ-aminobutyric acid (GABA) instant white tea (GABA-IT) using GABA-enriched white tea as raw material, systematically characterizing its chemical composition and volatile profile. In contrast to the conventional instant tea production process, this work integrates response surface methodology with spray-drying parameter optimization. This integrated approach enables the simultaneous enhancement of functional components and sensory quality. A response surface design was employed to refine the extraction and spray-drying variables following preliminary single-factor trials, and the optimal parameter combination was subsequently determined (40% ethanol concentration, material-to-liquid ratio of 1:15, extraction time of 3 days, atomization speed of 300 rpm, and inlet temperature of 120 °C); the resulting GABA-IT exhibited significantly improved quality characteristics. Specifically, the GABA content increased by 209% (reaching 4.42 mg/g), and theanine, catechins, and caffeine were enriched by 200-300%. Regarding volatile profiles, processing led to a reduction in esters but an increase in aldehydes and hydrocarbons. Relative odor activity value (rOAV) analysis revealed that epoxy-β-ionone and linalool were the key contributors to the characteristic aroma of GABA-IT. Collectively, this study demonstrates the technical feasibility of producing GABA-rich instant tea with enhanced functional components and improved sensory quality, providing practical guidance for the large-scale industrial production of functional tea beverages.

02
CLINICAL STUDY Frontiers in integrative neuroscience (2025) PMID: 41695889 ↗
Kiperin Mind Focus supplement mitigates chronic stress-induced neuroinflammation and molecular dysregulation and improves stress-related affective and exploratory behaviors in rats.
Clinical Trial Synthesis 2025 Randomized Controlled Trial (RCT) published in Frontiers in integrative neuroscience. Key conclusion: CONCLUSION: Kiperin Mind Focus exerted robust neuroprotective, anti-inflammatory, and antioxidant effects under chronic stress, restoring molecular homeostasis and stabilizing stress-relat
View Original PubMed Abstract ↓

BACKGROUND: Chronic stress is known to impair emotional regulation and adaptive behavioral responses through neuroinflammatory activation, oxidative imbalance, and dysregulation of neuroplasticity-related genes. Kiperin Mind Focus, a nootropic nutraceutical containing L-theanine, citicoline, phosphatidylserine, Rhodiola rosea, Ginkgo biloba, caffeine, and Lion's Mane mushroom extract has been formulated to support stress resilience, mood regulation and neural health. This study aimed to investigate the neuroprotective and neuroregulatory effects of the combined formulation on behavioral, biochemical, histopathological, and molecular parameters in rats exposed to chronic unpredictable mild stress (CUMS). METHODS: Thirty-two adult male Wistar rats were randomized into four groups (n = 8): Control, Stress, Kiperin Mind Focus (MF), and Stress + Mind Focus (SMF). CUMS was applied for 45 days, and the combined formulation was administered by oral gavage (130 mg/kg/day). Behavioral outcomes were evaluated using the sucrose preference (SPT), open field (OFT), elevated plus maze (EPM), and forced swim (FST) tests. Serum and tissue cytokine levels (IL-1β, IL-6, IL-10, TNF-α) and oxidative stress index (TOS/TAS ratio) were measured. Hippocampal and prefrontal gene expression of FOS, DBH, NMB, BDNF, CREB1, GRIN2A, and GABRB1 was assessed via qPCR, and histopathological changes were semi-quantitatively scored. RESULTS: Chronic stress induced anhedonia, anxiety-like behavior, and behavioral despair, accompanied by elevated proinflammatory cytokines, oxidative imbalance, and neuronal degeneration in the hippocampus and prefrontal cortex. The supplementation significantly improved SPT, OFT, EPM, and FST performance, normalized cytokine and oxidative parameters, and reduced neuronal injury scores. At the molecular level, supplementation attenuated stress-induced upregulation of FOS, DBH, and NMB while maintaining neurotrophic (BDNF, CREB1) and GABAergic (GABRB1) expression near control levels. CONCLUSION: Kiperin Mind Focus exerted robust neuroprotective, anti-inflammatory, and antioxidant effects under chronic stress, restoring molecular homeostasis and stabilizing stress-relat

03
RANDOMIZED TRIAL (RCT) Frontiers in nutrition (2025) PMID: 41668720 ↗
Acute effects of combined and isolated caffeine and theanine supplementation on physical and cognitive performance in competitive athletes: a randomized, double-blind, placebo-controlled crossover study.
Clinical Trial Synthesis 2025 Randomized Controlled Trial (RCT) published in Frontiers in nutrition; statistical significance reported at p = 0.004. Key conclusion: Finally, acute ingestion of TEA was associated with reduced maximal isometric leg and back strength compared with CAF and CON.
View Original PubMed Abstract ↓

INTRODUCTION: Modern athletic performance is driven not only by physical capacity but also by rapid decision-making, attentional control, and visuomotor coordination. Evidence regarding the acute effects of caffeine (CAF), L-theanine (TEA), and their combination remains inconsistent, particularly with respect to their combined influence on physical and cognitive performance in athletic populations. This study examined the acute effects of isolated and combined CAF and TEA supplementation on maximal strength, intermittent aerobic endurance, and eye-hand coordination in competitive athletes. It was hypothesized that the combined ingestion of CAF and TEA would differentially affect physical performance and eye-hand coordination outcomes compared with isolated CAF or TEA intake. METHODS: Twenty trained athletes completed four randomized, double-blind, placebo-controlled crossover conditions: CAF (3 mg·kg-1), TEA (200 mg), CAF+TEA (COM), and placebo (CON), with ≥72 h washout. Outcomes included isometric leg, back, and handgrip strength; Yo-Yo Intermittent Endurance Test Level 1 performance; and visuomotor coordination (CogniFit®). Data were analyzed using repeated-measures ANOVA with Bonferroni corrections (α = 0.05). RESULTS: Condition effects were found for leg strength (p = 0.004, ηp2 = 0.24) and back strength (p = 0.008, ηp2 = 0.19). In the COM condition, no additional or synergistic effect on maximal strength was observed. Additionally, no significant difference was found between the conditions in aerobic endurance, maximum isometric handgrip strength, and hand-eye coordination results. Caffeine ingestion did not differ from placebo for any strength outcome under the present conditions. Finally, acute ingestion of TEA was associated with reduced maximal isometric leg and back strength compared with CAF and CON. DISCUSSION: Findings challenge the prevailing assumption of CAF + TEA synergy and underscore the need for task-specific interpretation of co-supplementation strategies. Future studies should evaluate dose-response interactions, habitual caffeine intake, sex-specific responses, and broader cognitive domains beyond visuomotor control. The randomized control

04
CLINICAL STUDY Food research international (Ottawa, Ont.) (2026) PMID: 41652690 ↗
Identification and quality evaluation of Camellia sinensis cv. Longjing 43 fresh leaves from Enshi with different altitudes based on non-targeted metabolomics combined with chemometrics.
Clinical Trial Synthesis 2026 Clinical Study published in Food research international (Ottawa, Ont.); statistical significance reported at p = 0.05. Key conclusion: The RF ensemble structure helped reduce overfitting on high-dimensional metabolomic data and quantify feature importance, facilitating identification of key altitude biomarkers such as 1,2,3-tri-O-galloyl-β-d-glucose and Galloylprocyanidin B4.
View Original PubMed Abstract ↓

The quality of green tea is closely related to its growing environment, especially the altitude. In the present study, the intrinsic relationship between green tea raw materials and altitude was investigated by using machine learning in chemometric analysis. Forty-six Camellia sinensis cv. Longjing 43 (LJ43) samples from three altitude ranges (U500, 500-799, H800) were collected and the basic component analysis and non-target metabolomics were conducted. Results revealed significant altitude-dependent trends that tea polyphenols, total catechins (EGCG, EC, C, GC, EGC), and caffeine decreased with the increasing altitude, while the total free amino acids include theanine, soluble sugars, ECG, and CG increased. Additionally, seventy-four altitude-specific metabolites were identified by using dual thresholds of VIP ≥ 1 and P < 0.05, and the multiple machine learning algorithms were further employed to classify the altitude of raw materials. On the test set, the Random Forest (RF) model achieved the highest accuracy of 97.5 %, outperforming Support Vector Machine (SVM) at 95.24 % and K-Nearest Neighbors (KNN) at 82.5 %. The RF ensemble structure helped reduce overfitting on high-dimensional metabolomic data and quantify feature importance, facilitating identification of key altitude biomarkers such as 1,2,3-tri-O-galloyl-β-d-glucose and Galloylprocyanidin B4. In contrast, linear SVM struggled with nonlinear patterns, while KNN was adversely affected by the irrelevant features. This study demonstrated that metabolites were closely related to the altitude. Nontargeted metabolomics analysis coupled with machine learning functions as a powerful approach to establish chemical fingerprint maps of raw materials and their environment.

05
CLINICAL STUDY Diabetes/metabolism research and reviews (2026) PMID: 41431168 ↗
Unravelling the Mechanisms of Tea Against NAFLD: An Integration of Bibliometrics, Network Pharmacology, and the Gut-Liver Axis.
Clinical Trial Synthesis 2026 Clinical Study published in Diabetes/metabolism research and reviews. Key conclusion: This consolidated mechanistic framework not only provides a comprehensive understanding of tea's anti-NAFLD effects but also highlights the significant potential for developing targeted, tea-based nutraceuticals and pharmaceuticals.
View Original PubMed Abstract ↓

Non-alcoholic fatty liver disease (NAFLD) represents a significant global health challenge with limited therapeutic options. Tea consumption has emerged as a promising preventive and therapeutic strategy, yet a systematic and integrative understanding of its mechanisms is lacking. This review employs a novel tripartite approach-combining bibliometric analysis, network pharmacology, and an in-depth literature review-to comprehensively elucidate the multi-faceted role of tea in combating NAFLD. The bibliometric analysis identifies 'inflammation,' 'steatosis,' 'insulin resistance,' and 'gut microbiota' as the core research hotspots. Network pharmacology predicts that tea's active constituents target key proteins (e.g., VEGFA, CDK1) to regulate pivotal pathways like P53 and cancer signalling. We further synthesise evidence on how specific components, such as EGCG and yellow tea polysaccharides, modulate pathways including NF-κB and FXR to alleviate oxidative stress, inflammation, and hepatic steatosis. A central mechanistic insight elucidated in this review revolves around the gut-liver axis. We emphasise that despite their low systemic bioavailability, tea polyphenols exert potent prebiotic-like effects. They are metabolised by the gut microbiota into smaller, more bioavailable phenolic acids and other metabolites that retain or even enhance bioactivity. Furthermore, tea polyphenols, polysaccharides, caffeine, and theanine collectively modulate microbial community structure, enhance the production of beneficial metabolites such as short-chain fatty acids, and reinforce intestinal barrier function, thereby collectively ameliorating the progression of NAFLD. This consolidated mechanistic framework not only provides a comprehensive understanding of tea's anti-NAFLD effects but also highlights the significant potential for developing targeted, tea-based nutraceuticals and pharmaceuticals. Moreover, it establishes a scientific basis for guiding scientifically informed tea consumption practices for the management of NAFLD. © 2025 John Wiley & Sons Ltd.

06
CLINICAL STUDY Food chemistry (2025) PMID: 41312199 ↗
Identification and quality evaluation of Fuyun 6 and Zhongcha 108 tea fresh leaves at different altitudes using non-targeted metabolomics combined with machine learning.
Clinical Trial Synthesis 2025 Clinical Study published in Food chemistry. Key conclusion: A significant cultivar × altitude interaction was observed for coumarin.
View Original PubMed Abstract ↓

Tea cultivar and growing altitude are key factors shaping tea quality. This study systematically investigated their individual and synergistic effects on the quality of fresh leaves of Zhongcha 108 (ZC108) and Fuyun 6 (FY6), which were collected at altitudes from 442 to 945 m. Chemical analysis revealed that ZC108 had higher levels of amino acids, theanine, sugars, flavonoids, and catechins than FY6. Increasing altitude reduced tea polyphenols, flavonoids, caffeine, and catechins in both cultivars. Non-targeted metabolomics identified 50 cultivar and 40 altitude-associated metabolites. Key metabolic pathways, including phenylpropanoid, purine, and flavonoid biosynthesis, were upregulated with increasing altitude. A significant cultivar × altitude interaction was observed for coumarin. Machine learning achieved 100 % accuracy in cultivar classification (RF: 96.7 %, SVM: 93.3 %, KNN: 90 %), highlighting the cultivar factors dominance. Key biomarkers, such as phenylethanol and 6-O-β-D-fructofuranosyl-d-glucose were identified. These findings provide a basis for tea cultivar identification, origin traceability, and quality control. © 2025 The Authors. Published by Elsevier Ltd.

07
CLINICAL STUDY Food chemistry (2026) PMID: 41297472 ↗
Multi-scale quality evaluation and geographical origins discrimination of Ankang green tea by intelligent sensory analysis, selenium elemental analysis and quantitative non-volatile sensometabolomics.
Clinical Trial Synthesis 2026 Clinical Study published in Food chemistry. Key conclusion: Moreover, the correlation between differential metabolites, selenium, and taste indexes was explored.
View Original PubMed Abstract ↓

To date, no comprehensive study has explored the multi-dimensional quality of Ankang selenium-enriched green tea. Herein, 61 Ankang tea samples from four small-scale geographical origins were analyzed using a novel multi-analytical approach combining intelligent sensory evaluation, selenium quantification, and sensometabolomics. Selenium content differed across regions. 89 non-volatiles were absolutely quantified. Flavan-3-ols were most abundant (493.79-1317.04 mg/L), followed by amino acids (406.18-940.11 mg/L), phenolic acids (364.66-901.33 mg/L), alkaloids (355.44-688.72 mg/L), organic acids (121.08-556.10 mg/L), sugars (105.88-511.91 mg/L), flavone/flavonol and glycosides (0.62-48.48 mg/L). Epigallocatechin gallate (EGCG), theanine, theogallin, caffeine, citric acid, maltose, and kaempferol-3-O-glucosylrutinoside were most predominant within each class. Dose-over-threshold (DOT) based taste contribution analysis showed 10 compounds with DOT>1, highlighting rutin, theogallin, EGCG and caffeine as prominent contributors (DOT = 2036.82, 10.44, 7.28, 5.31, respectively). 43 key differential compounds and distinct DOT in astringency, bitterness and umami was revealed across regions. Moreover, the correlation between differential metabolites, selenium, and taste indexes was explored.

08
CLINICAL STUDY Food chemistry (2025) PMID: 41080130 ↗
Metabolic insights into the enhanced umami and sweetness of small-leaf yellow tea from albino cultivars.
Clinical Trial Synthesis 2025 Clinical Study published in Food chemistry. Key conclusion: These findings support the conclusion that the combination of elevated AA levels and reduced catechin levels is the primary driver of the fresh sweet taste of albino cultivars.
View Original PubMed Abstract ↓

Albino cultivars are well suited for producing small-leaf yellow tea because of their unique leaf colour and taste. This study aimed to uncover the chemical basis for the fresh sweet taste and low bitterness/astringency of albino cultivars through metabolomics. We identified 20 core taste compounds, namely 13 flavonoids, 5 amino acids (AAs), and 2 catechins. Compared with the control 'Fudingdabaicha', 'Naibai' contained a higher number of umami AAs (theanine: 45.84 mg/g; glutamic acid: 10.27 mg/g) and lower catechin levels. Quantitative descriptive analysis showed that albino cultivars exhibited stronger umami and sweetness but reduced bitterness and astringency, suggesting that umami compounds can mitigate the perception of bitterness and astringency. Weighted gene co-expression network analysis indicated that AAs are associated with umami taste, whereas flavonoids, catechins, and caffeine influence bitterness and astringency. These findings support the conclusion that the combination of elevated AA levels and reduced catechin levels is the primary driver of the fresh sweet taste of albino cultivars. © 2025 The Authors.

09
CLINICAL STUDY Journal of agricultural and food chemistry (2025) PMID: 41066656 ↗
Effects of Arbuscular Mycorrhizal Fungi on Growth and Selenium Accumulation in Tea Plants (Camellia sinensis).
Clinical Trial Synthesis 2025 Clinical Study published in Journal of agricultural and food chemistry. Key conclusion: These results indicate that AMF promotes earlier bud sprouting─enabling earlier market entry─and improves Se fertilizer use efficiency, thereby reducing input costs.
View Original PubMed Abstract ↓

Arbuscular mycorrhizal fungi (AMF) enhance host biomass and nutrient uptake, yet their regulatory mechanisms and gene networks in tea plants remain unclear. This study investigated AMF-induced effects on bud sprouting, selenium (Se) accumulation, secondary metabolite contents, and transcriptome profile changes in tea plants to elucidate these mechanisms. The results showed that AMF accelerated tea bud sprouting by 1 week, increased available Se content in rhizosphere soil and leaves, and elevated l-theanine content while decreasing polyphenols and caffeine levels. The green tea produced under AMF inoculation combined with 100 mg/L Na2SeO3 received the highest sensory score. Differential gene expression analysis identified 980, 3099, and 1044 differentially expressed genes in the comparisons of CK vs Se, CK vs AMF, and CK vs Se + AMF, respectively. These results indicate that AMF promotes earlier bud sprouting─enabling earlier market entry─and improves Se fertilizer use efficiency, thereby reducing input costs. This study provides a theoretical basis for elucidating the molecular mechanisms of tea tree-microbe interactions.

10
CLINICAL STUDY Foods (Basel, Switzerland) (2025) PMID: 41008167 ↗
Effects of Different Fertilization Patterns on the Content of Quality Indices and the Formation of Aroma Characteristics of Tea Leaves.
Clinical Trial Synthesis 2025 Clinical Study published in Foods (Basel, Switzerland). Key conclusion: This study provides a theoretical basis for optimizing the fertilization strategy of tea bushes to improve tea quality.
View Original PubMed Abstract ↓

Fertilization is a necessary measure in the cultivation and management of the tea bush, and the use of different fertilizers significantly affects the quality of tea leaves. In this study, 100% chemical fertilizer (CF), 100% organic fertilizer (OF), and 50% chemical fertilizer + 50% organic fertilizer (COF) were used to analyze the effects of different fertilizer treatments on the quality indices and volatile component compositions of tea leaves. The results showed that COF treatment significantly increased the content of water extract, tea polyphenols, theanine, free amino acids, and soluble sugar, but decreased the content of total flavonoids and caffeine, indicating that COF treatment has an advantage in improving the overall quality of tea leaves. Analysis of volatile components showed that different fertilizer treatments significantly affected the content of eleven characteristic metabolites in tea bush leaves, of which four characteristic metabolites were most abundant under CF treatment, eight under OF treatment, and only one under COF treatment. The odor characteristics and their intensity analyses showed that the 11 characteristic volatile components mainly exhibited three types of odor characteristics, such as woody, green, and floral, of which OF treatment enhanced woody and green intensities, while CF treatment enhanced floral intensity. Taken together, different fertilizer treatments could regulate the quality indices and volatile components of tea leaves, while the use of chemical fertilizers or organic fertilizers alone was conducive to enhancing the intensity of individual special odor characteristics in tea leaves. Overall, the combination of chemical fertilizers and organic fertilizers was more conducive to the improvement of tea quality. This study provides a theoretical basis for optimizing the fertilization strategy of tea bushes to improve tea quality.

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