Glyceryl tribenzoate: A food additive with unique properties to be a substitute for cinnamon.


Journal

Journal of clinical & experimental immunology
Titre abrégé: J Clin Exp Immunol
Pays: United States
ID NLM: 101697507

Informations de publication

Date de publication:
2021
Historique:
entrez: 1 11 2021
pubmed: 2 11 2021
medline: 2 11 2021
Statut: ppublish

Résumé

Cinnamon is a regularly used natural seasoning and flavoring material throughout the world for eras. Recent laboratory studies have demonstrated that oral cinnamon may be beneficial for different neuroinflammatory and neurodegenerative disorders such as multiple sclerosis (MS), Parkinson's disease (PD), Alzheimer's disease (AD), and Lewy body diseases (LBD). However, cinnamon's certain limitations (e.g. unavailability of true Ceylon cinnamon throughout the world, impurities in ground cinnamon, etc.) have initiated an interest among researchers to find an alternate of cinnamon that can potentially deliver the same efficacy in the diseases mentioned above. Glyceryl tribenzoate (GTB) is a U.S. Food and Drug Administration (FDA)-approved flavoring ingredient that is used in food and food packaging industries. It has been found that similar to cinnamon, oral GTB is capable of upregulating regulatory T cells and suppressing the autoimmune disease process of experimental autoimmune encephalomyelitis, an animal model of MS. Moreover, both GTB and cinnamon metabolite sodium benzoate (NaB) have the potency to attenuate neurodegenerative pathology in a mouse model of Huntington disease (HD). Here, we have also demonstrated anti-inflammatory property of GTB in astrocytes and macrophages, a property that is also seen with cinnamon and its metabolite sodium benzoate (NaB). Therefore, here, we have made a sincere attempt to discuss the similarities and dissimilarities between cinnamon and GTB with a focus whether GTB has the potential to be considered as a substitute of cinnamon for neuroinflammatory and neurodegenerative disorders.

Identifiants

pubmed: 34723288
doi: 10.33140/jcei.06.05.04
pmc: PMC8555914
mid: NIHMS1749969
doi:

Types de publication

Journal Article

Langues

eng

Pagination

367-372

Subventions

Organisme : BLRD VA
ID : I01 BX005002
Pays : United States
Organisme : BLRD VA
ID : IK6 BX004982
Pays : United States
Organisme : NCCIH NIH HHS
ID : R01 AT010980
Pays : United States

Déclaration de conflit d'intérêts

Conflicts of Interest: None

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Auteurs

Swarupa Pahan (S)

Division of Research and Development, Jesse Brown Veterans Affairs Medical Center, Chicago, USA.

Sridevi Dasarathi (S)

Department of Neurological Sciences, Rush University Medical Center, Chicago, USA.

Kalipada Pahan (K)

Division of Research and Development, Jesse Brown Veterans Affairs Medical Center, Chicago, USA.
Department of Neurological Sciences, Rush University Medical Center, Chicago, USA.

Classifications MeSH