Probiotic Effect on Dietary Nitrate to Plasma Nitrite Production ( OPEDNPN )

Background

Nitric oxide (NO) plays critical roles in a myriad of cellular and molecular mechanisms regulating physiology and function of various organs and systems.1,2 Low NO bioavailability contributes to pathology in multiple diseases including hemolytic anemias,3 malaria,4,5 transfusion of older stored blood,6,7 chronic heart failure,8 atherosclerosis,9 and diabetes.10 Recent reports suggest that the oral microbiome is linked with regulating NO homeostasis through the action of certain bacteria that have an ability to reduce nitrate to nitrite.11-15 Nitrite is then further reduced to NO through a variety of mechanisms in different tissues.16,17 Plasma nitrate is taken up back into the oral cavity by salivary glands so that the nitrate-nitrite-NO cycle provides sustained increases in NO bioavailability. Many clinical studies have used dietary nitrate as a source of NO through nitrite conversion.18-24 However, there is substantial variability in the clinical outcomes due to dietary nitrate intake and this is reflected in variability in the amount of nitrate converted to plasma nitrite.13,24-29 30. The variability and hence a large overall limitation in efficacy of dietary nitrate based treatments has been attributed to the capacity of the oral microbiome to reduce nitrate to nitrite.24-27 Preliminary work has begun to identify bacterial strains that are efficient nitrate to nitrite converters as well as those that actually inhibit nitrate to nitrite conversion.31,32 The efficiency of the nitrate-nitrite-NO cycle and the role of oral bacteria may contribute to normal health.11 Thus, understanding the variability in nitrate to nitrite conversion and aspects of the oral microbiome could lead to improvements in normal cardiovascular health. In addition, in order to maximize benefits from dietary nitrate interventions, we need to understand factors of the oral microbiome that affect nitrate to nitrite conversion. The investigators have recently discovered that several species of Lactobacillus produce a metabolite that blunts nitrate to nitrite conversion by other oral bacteria in vitro. Several of these Lactobacillus species are the main component of a commercially available oral probiotic, https://www.amazon.com/Dental-Probiotics-Breath-Gingivitis-Throat/dp/B096SZSFFS

Purpose

The purpose of this study is to determine if Lactobacillus will blunt dietary nitrate to plasma nitrite conversion.

The investigators hypothesize that the presence of oral Lactobacillus will blunt the conversion of dietary nitrate to plasma nitrite and will test this by comparing the conversion before and after use of this probiotic.

The main hypothesis rests on the auxiliary hypothesis that use of the oral probiotic will results in increased abundance of Lactobacillus in the oral cavity and will test this through genomic sequencing.

Methods OPEDNPN All eligible volunteers will be consented after learning about the study and agreeing to participate. Volunteers will be randomly assigned to one of two groups: (1) Probiotic and (2) Placebo. A total of 20 volunteers (10 per group) will participate in the study. The only difference for participants for each group will be whether they receive the placebo or probiotic.

All volunteers will participate in two visits: (1) Visit 1, baseline and (2) Visit 2, follow up. At each visit, volunteers will report to the Olin Physical Lab room 208 after having fasted for 3 hours prior. They can drink water one hour before the visit. Participants will be instructed not to use anti-bacterial mouthwash the day of the visit. The participant will be asked to provide 4 mL of saliva and a study team member will collect a bacterial sample from the posterior dorsal surface of their tongue (as described below). These samples will be frozen at -80 degrees for genetic analysis and identification of bacterial strains.

After saliva and tongue samples are collected, blood will be drawn (as described below) for plasma nitrite and nitrate determination. This blood sample will be the "pre-" sample collected at baseline and follow-up. Volunteers will then drink one 70 mL Beet it Sport Nitrate 400 shot (https://www.beet-it.us/pages/beet-it-sports). A "post-" blood draw will be collected 2.5 hours after consumption of the beetroot juice.

At Visit 1, after the second blood draw, volunteers will receive 7 days worth of either probiotic or the placebo. Volunteers will consume the probiotic (or placebo) as indicated by the manufacturer of the probiotic once a day. On day 8, the volunteers will return for visit 2.

The data will include (1) baseline and follow-up analysis of oral bacterial strains and (2) Pre- and post-beet juice consumption plasma nitrite and nitrate levels. The investigators hypothesize that the abundance of Lactobacillus will be higher at follow-up compared to baseline for volunteers taking the probiotic but that there will be no change in the placebo group. The investigators also hypothesize that the change in plasma nitrite (post minus pre) will be lower at follow-up than at baseline for volunteers taking the probiotic but that there will be no change in the placebo group.

• Study Materials (all commercially available):

• Placebo: Honest Placebo Pills by Zeebo
• Herbiotics Oral + Ent Probiotic
• Beet it Sport Nitrate 400 shot
• Collection of Saliva and Tongue scraping. Volunteers will report to the Olin Physical Lab room 208 after having fasted for 3 hours prior. They can drink water one hour before the visit. Participants will be instructed not to use anti-bacterial mouthwash the day of the visit. The participant will be asked to provide 4 mL of saliva by spitting into a microcentrifuge tube. For the tongue samples, a HydraFlock 6" Sterile Large Flock Swab w/Polystyrene Handle (Puritan Medical) will be used to collect scrapings. Volunteers will be asked to open their mouths as wide as possible and stick out their tongue. The posterior 1/3 of the dorsal surface of the tongue will be sampled by scraping lightly to moderately firmly the dorsal surface of the tongue back and forth Scraping will take a minute or so. The tongue scraping will be placed in 0.85 mL of buffered sterile saline and 0.15 mL glycerol. All samples will be frozen at -80°C and sent to Professor Hariom Yadav at the University of South Florida for genomic analysis.
• Blood draws and processing Blood will be drawn by a certified, trained phlebotomist. Blood samples (maximum ~10 mL) will be collected from participants following consent. Blood will be collected at each visit pre and 2.5 hours post beet juice consumption. Blood will be drawn as close to the 2.5 hour mark as possible. Realistically, it may occur between 2 to 3 hours after the final study beverage is consumed. Blood will be drawn by lab personnel with certified phlebotomy training via standard venipuncture methods or Tasso HemolinkTM device. The HemoLinkTM is an FDA-approved blood collection device that uses small lancets and gentle suction to collect a very small sample (~ ¼ teaspoons) of blood. Blood will be collected in standard blood collection tubes (e.g. citrate (blue-top), EDTA (purple-top) and heparin (green-top)) and labeled appropriately. The preferred tube is a 4 mL heparin tube. All blood samples drawn for research purposes will be identified by the study participant number and date/time of collection, which will also be recorded on the standardized data collection form. No personal identifying information will be included on the samples processed for research purposes. All blood samples will be immediately spun immediately in a centrifuge at 600-800g for five minutes and the supernatant collected. The plasma will be frozen on dry ice and then stored at -80°C for analysis of nitrite and nitrate content.
• Probiotic or placebo consumption Both the probiotic and placebo will be consumed twice a day according to instructions for the probiotic. One capsule is chewed or allowed to melt in the volunteer's mouth and then the contents are switched around in the mouth before being swallowed.

Risks Approximately 10 mL of blood will be drawn from patients willing to participate. This will be done in the usual fashion, preparing the venipuncture site with the local anesthetic EMLA, then drawing blood through a small gauge (23 or 21) butterfly needle. Drawing blood from a vein may be associated with discomfort or bruising at the site of needle puncture. Rarely, fainting or infection at the site of needle puncture may occur. All blood will be drawn from a person trained in phlebotomy. There will be no way to trace the blood back to the donor.

There are no known health risks for donating saliva or tongue scrapings from individuals who will be included in the study. There is a very minimal risk of linking individuals to the study. There will be no way to trace the saliva or tongue scrapings back to the donor.

Protections Against Risk Strategies for protection against risk. To protect privacy of participants and confidentiality of research data, no personal information regarding individual participants will be linked to the in vitro studies.

Plans for medical attention. In case of injury (which is extremely unlikely) as a result of saliva donation, the individuals will be instructed to contact their physician and medical care will be offered and charged to available research coverage maintained at Wake Forest School of Medicine.

In case of injury as a result of blood drawing, the patients will be instructed to contact their physician and medical care will be offered and charged to available research coverage maintained at Wake Forest School of Medicine. Blood drawn on the Reynolda campus is not a clinical setting, but blood will be drawn by trained phlebotomists with years of experience who maintain their training.

Any unanticipated problems, serious and unexpected adverse events, deviations or protocol changes will be promptly reported by the principal investigator or designated member of the research team to the IRB and sponsor or appropriate government agency if appropriate.

Incidental Findings. No incidental findings are expected to be discovered in this study as measures of bacterial nitrate reduction are not currently of clinical relevance so a strange, individual result in that measure would not be worth communicating.

Sample size assessment and statistical analysis

The investigators plan to enroll 10 participants who receive the probiotic and 10 participants who receive the placebo. The investigators hypothesize that, using a paired t-test, participants taking the probiotic will have significantly (P < .05) lower change in plasma nitrite (post minus pre) at follow up compared to baseline while there will be no significant effect of the placebo (paired t-test).

The Investigators calculated that they would have 80% power to measure a 75% decrease in the change in nitrite at follow-up compared to baseline for the probiotic group with 10 participants per group (Continuous endpoint Two independent samples). The investigators assumed a 60% standard deviation in the change in nitrite for follow-up vs baseline based on previous data from our lab.

Inclusion criteria

• Healthy adult volunteers ages 18-70

Exclusion criteria

• Individuals with a history of difficult blood draws. More than 2 blood draws in one week; on anti-coagulant or anti-platelet therapy (e.g. aspirin, Coumadin, etc.); known pregnancy; in police custody or a prisoner; common illness within 2 weeks of potential enrollment. The cumulative volume of blood drawn from a healthy adult over the prior eight-week period would exceed 550 ml including the current draw.
• In addition, individuals uncomfortable spitting into a tube, dry mouth (xerostomia) or dry eyes, Patients suffering from autoimmune diseases such as Sjogren's syndrome, rheumatoid arthritis, systemic lupus erythematosus, or progressive systemic sclerosis, since individuals with these autoimmune inflammatory diseases exhibit persistent xerostomia, individuals with active caries diagnosis or history of periodontitis