The effect of gum Arabic supplementation on cathelicidin expression in monocyte derived macrophages in mice.
Siednamohammeddeen. Nagat N; Badi. Rehab R; Mohammeddeen. Tahane T; Enan. Khalid K
Key Findings
- 15% (w/v) gum Arabic in drinking water for 28 days significantly increased CRAMP (mouse LL‑37) expression in monocyte‑derived macrophages (p = 0.023).
- 30% gum Arabic did not produce a statistically significant change in CRAMP expression (p = 0.055).
- The response appears dose‑dependent, with a lower concentration being more effective in this animal model.
Practical Outcomes
- Gum Arabic may act as a prebiotic that boosts innate immunity via higher cathelicidin levels, but evidence is limited to mice. For biohackers, it suggests trying low‑dose GA (around 15% w/v in water) could be worth exploring, while recognizing that human data are lacking and higher doses might not help.
Summary
In a mouse study, drinking water with 15% gum Arabic for four weeks raised the levels of the immune‑boosting peptide cathelicidin (the mouse version of human LL‑37) in immune cells, while a higher 30% dose did not show a clear benefit. The effect seems to depend on the amount of gum Arabic, but the work was done in mice, not people.
Abstract
Antimicrobial peptides (AMPs) are important effectors of the innate defense system. Cathelicidins, (CRAMP in mouse/rat, LL-37 in human) is one of the two major classes of AMPs in humans. The upregulation of LL-37 synthesis is a novel non-antibiotic approach to prevent or treat infectious diseases. Butyrate was found to induce Cathelicidin expression. Gum Arabic (GA), an exudate from Acacia senegaltree, is known for its prebiotic effects. Fermentation of GA by colonic bacteria increases serum butyrate concentrations. This study was conducted to investigate if GA supplementation can increase Cathelicidin expression in macrophages. The study was an in-vivo experiment in mice. Thirty mice were randomly divided into three groups, ten mice per group. The two intervention groups received GA dissolved in drinking water in two different concentrations (15% w/v and 30% w/v) for 28 days. The third group served as a control. Blood was collected on Day 29 to isolate peripheral blood mononuclear cells (PBMC) which were cultured to obtain monocyte derived macrophages (MDMs). The transcription level of CRAMP was determined in MDMsby qPCR. We detected a significant increase (p = 0.023) in CRAMP expression in MDMs following 28 days of 15% GA supplementation, compared to the control group, but there was no significant change in the group on 30% GA supplementation (p = 0.055). GAsupplementation can induce Cathelicidin expression in MDMs and the effect is dose dependent.
Study Information
pubmed
2022
2022-06-01T00:00:00.000Z
10.1186/s12906-022-03627-9
7
54