# Botulinum Toxin Effects and Its Association with Vitamin and Mineral Supplementation: A Narrative Review

**Authors:** Ema Puizina, Dinko Martinovic, Slaven Lasic, Lovre Martinovic, Jasna Puizina, Emil Dediol, Slaven Lupi-Ferandin, Josko Bozic

PMC · DOI: 10.3390/nu18030491 · Nutrients · 2026-02-02

## TL;DR

This review explores how vitamins and minerals might affect the outcomes of botulinum toxin treatments, finding limited and inconsistent evidence.

## Contribution

The paper provides a comprehensive narrative review on the interaction between botulinum toxin and vitamin/mineral supplementation.

## Key findings

- Zinc supplementation may influence BoNT effects in facial applications, but results are inconsistent.
- Copper may antagonize BoNT in animal models, while magnesium and calcium have theoretical but unproven roles.
- Vitamin E increases bruising risk, and vitamin D affects baseline muscle strength and dosing needs.

## Abstract

Background: With the emerging global popularity of botulinum neurotoxin (BoNT), both for aesthetical and medical purposes, there is a rising need for achieving better outcomes. The aim of this narrative review was to comprehensively cover the effect of BoNT, as well as its possible interactions with everyday mineral and vitamin supplementation. Results: It is well established that BoNT exerts its paralytic effects through zinc-dependent cleavage of SNARE proteins, blocking acetylcholine release at the neuromuscular junctions. However, after meticulous research of the available literature regarding the effect of oral supplementation on BoNT, there is very scarce data. The effect of zinc supplementation on the duration and effectiveness of BoNT in some facial applications was studied in a couple of clinical studies; however, systematic reviews indicate inconsistent results. Copper acts as a noncompetitive inhibitor, potentially antagonizing BoNT in animal models. Magnesium and calcium exhibit theoretical synergistic or compensatory roles via neuromuscular transmission modulation but lack clinical validation. Vitamin B complex shows no interference in rat studies and vitamin D influences baseline muscle strength and dosing needs, while vitamin E increases bruising risk but not efficacy. Conclusions: Even though zinc supplementation holds promise for potentiating BoNT effects, evidence for both zinc and other supplements remains speculative or contradictory, underscoring the need for randomized controlled trials to develop evidence-based guidelines. Clinicians should assess patient supplementation status pre-treatment to optimize outcomes and minimize complications, particularly advising against high-dose vitamin E peri-procedurally.

## Linked entities

- **Chemicals:** zinc (PubChem CID 23994), copper (PubChem CID 23978), magnesium (PubChem CID 5462224), calcium (PubChem CID 5460341), vitamin E (PubChem CID 14985)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** SNAR-E (small NF90 (ILF3) associated RNA E) [NCBI Gene 100170220]
- **Diseases:** bruising (MESH:D003288)
- **Chemicals:** Copper (MESH:D003300), vitamin D (MESH:D014807), vitamin E (MESH:D014810), calcium (MESH:D002118), Magnesium (MESH:D008274), acetylcholine (MESH:D000109), zinc (MESH:D015032), Mineral (MESH:D008903)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

75 references — full list in the complete paper: https://tomesphere.com/paper/PMC12899707/full.md

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Source: https://tomesphere.com/paper/PMC12899707