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Cognitive and Cerebral Blood Flow Effects of Zanthozylum Armatum Fruit Extract in Healthy Adults Aged 30 - 55

The Acute and Chronic Cognitive and Cerebral Blood Flow Effects of Zanthozylum Armatum Fruit Extract: a Double Blind, Randomized, Placebo Controlled, Parallel Groups Study in Healthy Humans

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03673930
Enrollment
80
Registered
2018-09-17
Start date
2018-04-06
Completion date
2018-11-16
Last updated
2019-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Change

Keywords

NIRS, mood, cognitive performance, Zanthozylum armatum, Nepalese pepper

Brief summary

Zanthozylum armatum (Z. armatum)-otherwise known as Nepalese pepper, or timut-is an perennial shrub found in India and across Southeast Asia. Preparations of the bark, fruit and seeds of Z. armatum have been extensively used in traditional Indian medicine. Preliminary data have indicated that preparations of Z. armatum may also be beneficial to cognitive function. The study aims to investigate the effects acute and chronic consumption of Z. armatum on cognitive function and cerebral blood flow.

Detailed description

Zanthozylum armatum (Z. armatum) is an perennial shrub found in India and across Southeast Asia. Preparations of the bark, fruit and seeds of Z. armatum have been extensively used in traditional Indian medicine. For example, the fruits and seeds have been employed as an aromatic tonic in fever and dyspepsia and the essential oil of the fruits has exhibited antibacterial, antifungal and anthelmintic properties. Furthermore, the dried fruits are used as spice, especially in Nepalese and Sichuan cuisine with increasing popularity across Europe. With regard to physiological effects relevant to brain function, Z. armatum has also been traditionally used as a cardio-depressant; these vasodilatory properties have recently being linked to its antagonistic effect on calcium ion channel function as demonstrated in isolated rabbit aorta tissue. In addition, the observed anti-inflammatory and antioxidant effects of preparations of Z. armatum may serve to beneficially impact cognition with chronic administration. Although direct effects of Z. armatum on brain function have yet to be assessed; Zanthozylum fruit comprises one constituent of the traditional Japanese herbal medicine Daikenchuto (DKT) where some data do exist. In a series of trials investigating the effects of DKT on learning and memory function in mice, it was established that the extract of Zanthozylum fruit contained in DKT alone that was associated with reductions in escape latency in the Morris Water Maze task. Interestingly, the authors also revealed that it was the amide hydroxy-ɑ-sanshool (HAS) isolated from the Zanthozylum fruit extract that was associated with these effects, speculating that the effect of HAS on escape latencies was due to a facilitation effect of HAS on acetylcholine release. Given the evidence of potentially relevant mechanisms of action and initial evidence of cognitive effects of HAS in murine models, the aim of this study is to assess the acute and chronic effects of Z. armatum on cognitive function, mood, and cerebral blood flow in healthy adults aged 30 to 55 years.

Interventions

DIETARY_SUPPLEMENTZanthozylum armatum

Zanthozylum armatum MCT oil extract

DIETARY_SUPPLEMENTPlacebo

sunflower oil matched for appearance

Sponsors

Mibelle AG
CollaboratorINDUSTRY
Northumbria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants must self-assess themselves as being in good health * Aged 30 to 55 years at the time of giving consent * Are proficient in English equivalent to IELTS band 6 or above

Exclusion criteria

* Have any pre-existing medical condition/illness which will impact taking part in the study NOTE: the explicit exceptions to this are controlled (medicated) hypertension, arthritis, asthma, hay fever, high cholesterol and reflux-related conditions. There may be other, unforeseen, exceptions and these will be considered on a case-by-case basis; i.e. participants may be allowed to progress to screening if they have a condition/illness which would not interact with the active treatments or impede performance * Are currently taking prescription medications or dietary supplements including omega fatty acids / fish oils NOTE: the explicit exceptions to this are hormone replacement treatments for female participants where symptoms are stable, those medications used in the treatment of arthritis, high blood pressure, high cholesterol and reflux-related conditions; and those taken 'as needed' in the treatment of asthma and hay fever. As above, there may be other instances of medication use which, where no interaction with the active treatments is likely, participants may be able to progress to screening * Have planned a surgery requiring general anaesthesia * Have high blood pressure (systolic over 159 mm Hg or diastolic over 99 mm Hg) * Have a Body Mass Index (BMI) outside of the range 18-35 kg/m2 * Are pregnant, seeking to become pregnant or lactating * Have learning difficulties, dyslexia * Have a visual impairment that cannot be corrected with glasses or contact lenses (including colour-blindness) * Smoker or regular consumption of nicotine containing products e.g. patches, gum, vaping * Have a history of alcohol or drug abuse * Excessive caffeine intake (\>500 mg per day) * Have food intolerances/sensitivities, especially against citrus fruits * Have any health condition that would prevent fulfilment of the study requirements * Are unable to complete all of the study assessments * Are currently participating in other clinical or nutrition intervention studies, or have in the past 4 weeks * Do not have a bank account (required for payment) * Are non-compliant with regards treatment consumption

Design outcomes

Primary

MeasureTime frameDescription
Secondary memory scoreChronic (57 days)This is a composite measure derived from summing the z score performance on the following cognitive tasks: immediate word recall, delayed word recall, delayed picture recognition, delayed word recognition, delayed name to face recall (-1 to 1 where higher is better).

Secondary

MeasureTime frameDescription
Name to face recall correct responsesAcute (45, 180, 300 minutes post-dose)number (0-24; higher is better)
STAI-trait total scoreBaselineState-trait anxiety inventory 'trait' score (20-80; higher is more anxious)
STAI-state total scoreChronic (57 days)State-trait anxiety inventory 'state' score (20-80; higher is more anxious)
Secondary memory scoreAcute (45, 180, 300 minutes post-dose)This is a composite measure derived from summing the z score performance on the following cognitive tasks: immediate word recall, delayed word recall, delayed picture recognition, delayed word recognition, delayed name to face recall (-1 to 1 where higher is better).
Working memory scoreChronic (57 days)This is a composite measure derived from summing the z score performance on the numeric working memory task and Corsi block-tapping task (-1 to 1; where higher is better)
Speed of memory scoreAcute (45, 180, 300 minutes post-dose)This is a composite measure derived from summing the z score reaction times on the numeric working memory task, the delayed name/face recall task, the delayed picture recognition task, and the delayed word recognition task (-1 to 1; where lower is better).
Accuracy of attention scoreAcute (45, 180, 300 minutes post-dose)This is a composite measure derived from summing the z score accuracy performance on the choice reaction time and Rapid visual information processing tasks (-1 to 1; where higher is better)
Speed of attention scoreAcute (45, 180, 300 minutes post-dose)This is a composite measure derived from summing the z score reaction times on the choice reaction time and Rapid visual information processing tasks (-1 to 1; where lower is better)
Immediate word recall task correctly identified wordsAcute (45, 180, 300 minutes post-dose)total number (0-15; where higher is better)
Immediate word recall task error responsesAcute (45, 180, 300 minutes post-dose)total number (can be any number; lower is better)
Delayed word recall task correctly identified wordsAcute (45, 180, 300 minutes post-dose)total number (0-15; where higher is better)
Delayed word recall task correctly error responsesAcute (45, 180, 300 minutes post-dose)total number (can be any number; lower is better)
Picture recognition accuracyAcute (45, 180, 300 minutes post-dose)(%; 0-100; where higher is better)
Picture recognition reaction timeAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Word recognition accuracyAcute (45, 180, 300 minutes post-dose)(%; 0-100; where higher is better)
Name to face recall reaction timeAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Peg and ball task planning timeAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Peg and ball task completion timeAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Peg and ball task errorsAcute (45, 180, 300 minutes post-dose)number (can be any number, lower is better)
Corsi blocks accuracyAcute (45, 180, 300 minutes post-dose)Average scores from the last five correctly completed trials from the corsi block-tapping task
Choice reaction time accuracyAcute (45, 180, 300 minutes post-dose)(%; 0-100; where higher is better)
Choice reaction time reaction timeAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Numeric working memory accuracyAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Numeric working memory reaction timeAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Serial 3 subtractions total responsesAcute (45, 180, 300 minutes post-dose)number - calculated from the 3 cycles of the Cognitive Demand Battery; higher is better
Serial 3 subtractions total error responsesAcute (45, 180, 300 minutes post-dose)number - calculated from the 3 cycles of the Cognitive Demand Battery; lower is better
Serial 7 subtractions total responsesAcute (45, 180, 300 minutes post-dose)number - calculated from the 3 cycles of the Cognitive Demand Battery; higher is better
Serial 7 subtractions total error responsesAcute (45, 180, 300 minutes post-dose)number - calculated from the 3 cycles of the Cognitive Demand Battery; lower is better
Rapid visual information processing accuracyAcute (45, 180, 300 minutes post-dose)(%) - calculated from the 3 cycles of the Cognitive Demand Battery (%; 0-100; where higher is better)
Rapid visual information processing reaction timeAcute (45, 180, 300 minutes post-dose)(ms) - calculated from the 3 cycles of the Cognitive Demand Battery; lower is better
Rapid visual information processing false alarmsAcute (45, 180, 300 minutes post-dose)number - calculated from the 3 cycles of the Cognitive Demand Battery; lower is better
Mental fatigueAcute (45, 180, 300 minutes post-dose)visual analogue scale (%) - calculated from the 3 cycles of the Cognitive Demand Battery (0-100; higher indicates more fatigue)
Subjective mood - AlertAcute (45, 180, 300 minutes post-dose)derived from Bond Lader visual analogue scales (0-100; higher is more alert)
Subjective mood - Content (visual analogue scale)Acute (45, 180, 300 minutes post-dose)derived from Bond Lader visual analogue scales (0-100 higher is more content)
Word recognition reaction timeAcute (45, 180, 300 minutes post-dose)(ms; lower is better)
Subjective mood - CalmAcute (45, 180, 300 minutes post-dose)derived from Bond Lader visual analogue scales (0-100 higher is more calm)
Subjective mood - Calm (Bond Lader visual analogue scale)Superimposed chronic (57 days plus 45, 180, 300 minutes post-dose)derived from Bond Lader visual analogue scale (0-100 higher is more calm)
Cerebral blood flow during performance of cognitive tasksAcute (120, 150 minutes post-dose)Measured (in umol) using quantitative near infrared spectroscopy (higher indicates increased blood volume)
Cerebral blood flow at restAcute (120, 150 minutes post-dose)Measured (in umol) using quantitative near infrared spectroscopy (higher indicates increased blood volume)
Subjective mood - ContentChronic (57 days)derived from Bond Lader visual analogue scales(0-100 higher is more content)

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026