Cognitive decline
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. There were 30 healthy adults aged 18~45, 15 males and 15 females; 2. All female participants ensured that they did not use oral hormonal contraceptives and had no intention of new pregnancy during the intervention; 3. Sign a dated written informed consent.
Exclusion criteria
Exclusion criteria: 1. Suffering from stomach pain, bloating, constipation, diarrhea, cardiovascular disease (stroke, heart failure, coronary heart disease, and peripheral artery disease), blood disease, cancer, diabetes, hypertension, renal insufficiency (EGFR 30 kg/m^2), claustrophobia, epilepsy, high risk of depression (cesd-10 score >= 10), or depression, and history of nicotine product use; 2. Current pregnancy, or suspected metal foreign bodies in the eyeball and beside the great vessels after the installation of cardiac pacemakers, internal fixation metal implants, automatic cardioverter defibrillators, functional nerve stimulators, cardiac stents, artificial heart valves, metal clips after aneurysm surgery; 3. Those who do not agree to sign the informed consent of patients; 4. Those who have taken antibiotics, or non-steroidal anti-inflammatory drugs within 3 months, or have the habit of eating probiotic products and change the type of probiotics they eat within the recent 1 month; 5. Addicts to cigarettes, alcohol, and drugs; 6. The basic salt intake is more than 8 g / day; 7. People who are allergic to lactulose and gelatin or have dietary restrictions on lactose and gelatin.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| FMRI analysis results; | — |
Secondary
| Measure | Time frame |
|---|---|
| AVLT-H score;Serum level of LPS binding protein;Serum level of S100ß;Composition of 16SrRNA fecal flora;Metabonomics of serum;Metabonomics of feces;24-hour urinary sodium;Lactulose recovery;mannitol recovery;lactulose / mannitol ratio; | — |
Countries
China
Contacts
Affiliated Hospital of Guangdong Medical University