Literature DB >> 32436164

Dietary fatty acids and the time elapsed from their intake are related to their composition in rat submandibular gland and salivary flow rates.

Jorge Escandriolo Nackauzi1,2, Gastón Repossi3, Claudio Bernal4, Adriana Actis3, Raquel Gallará5.   

Abstract

OBJECTIVES: The aim of this study was to analyze the influence of dietary fatty acids (FAs) and the time elapsed from their intake on FA tissue profile of rat submandibular gland (SG) and on its salivary flow rate (SFR). Do dietary FAs depending on the intake time modify their profile in SG and consequently the SFR?
MATERIALS AND METHODS: Thirty-six adult male Wistar rats were fed on control diet (corn oil, CD, 18:2 n-6 FA) for 7 days and then divided into CD and two groups with replacement of corn oil by olive (OD, 18:1 n-9 FA) or chia (ChD, 18:3 n-3 FA) oils (1 and 30 day intake). Submandibular ducts were canalized to collect saliva for 20 min (μL/min). SG were examined (optical/electron microscopy; ImageJ 1.48 software).
RESULTS: SFR values were 6.18 ± 0.34 (CD1), 6.04 ± 0.31 (OD1), and 6.00 ± 0.50 (ChD1) (p > 0.05). At 30-day intake, higher SFR values in ChD (7.82 ± 0.7) with respect to CD (4.68 ± 0.44; p < 0.001) and OD (6.08 ± 0.2; p = 0.038) were found. ChD30 showed a higher serous acinous area percentage than CD30 and OD30, whereas mucous acinous density was greater in CD30 than in OD30 and ChD30 (p < 0.05). α-Linolenic (ALA) and eicosapentaenoic and docosahexaenoic acid levels were only detected in SG of ChD30, while arachidonic acid was lower in this group as compared with CD30 and OD30 (p < 0.05).
CONCLUSIONS: SG FA composition and its SFR appear to be modulated by dietary FAs and the time elapsed from their consumption. SFR is highest with n-3 ALA-rich ChD at 30-day intake. CLINICAL RELEVANCE: Diet could contribute to improve secretory dysfunctions.

Entities:  

Keywords:  Dietary intake; Fatty acids; Salivary flow rates; Submandibular gland

Mesh:

Substances:

Year:  2020        PMID: 32436164     DOI: 10.1007/s00784-020-03285-6

Source DB:  PubMed          Journal:  Clin Oral Investig        ISSN: 1432-6981            Impact factor:   3.573


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