Dietary fibre digestion and fermentation of SCFA Flashcards

1
Q

Dietary fibre

A

-carbohydrates that are not digested or are poorly digested by enzymes in the small intestine
**non-starch polysaccharides

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2
Q

Predominant Non-starch Polysaccharides

A

-Cellulose
-Hemicellulose

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3
Q

Cellulose

A

-a linear unbranched chain of glucose with beta- (1,4) linkages
-tightly packed

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4
Q

Hemicellulose

A

-branched chain polysaccharide
>hexoses and pentoses

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5
Q

Where is hemicellulose commonly found?

A

-commonly found in grains as Xylan

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6
Q

Xylan

A

-xylose backbone with side chains composed of arabinose, mannose, galactose, and glucose

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7
Q

Insoluble plant fibres

A

-cellulose
-hemicellulose
-Lignin

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8
Q

Soluble plant fibres

A

-beta-glucans
-guar gum
-inulin, oligofructose, fructooligosaccharides
-pectins
-resistant starch

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9
Q

Manufactured soluble fibres

A

-psyllium
-polydextrose
-inulin
-oligosaccharides

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10
Q

Beat pulp

A

-combination of cellulose, hemicellulose, pectin, and lignin

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11
Q

Solubility vs. fermentability

A

-related terms but not equal
-can have low solubility and high fermentability and vice verse
-soluble: dissolve in water
-fermentability: metabolized by gut microbes

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12
Q

How does fibre effect the small intestine and stomach?

A

-delay gastric emptying (increased viscosity)
-promote satiety
>distension
>delayed gastric emptying
>release of satiety related hormones (GLP-1, PYY, CCK)
-reduced rate of nutrient absorption, reduced postprandial glucose and cholesterol absorption

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13
Q

How does fibre effect the colon?

A

-increased bacterial mass = increased stool mass
-increased rate of microbial fermentation =alters gut microbial composition and SCFA production
-excess can cause gastrointestinal intolerance (high intakes of rapidly fermentable)
-fermentation
>alter microbial composition
>production of SCFA

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14
Q

Dietary fiber in dogs

A

-no effect of high or low fermentable diets on insulin, PYY, GLP-1, or ghrelin

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15
Q

Fermentation in colon

A

-fermentation of fibre is a way to obtain energy
>fibre broken down into SCFAs (acetate,butyrate,proprionate)
-leads to proliferation of colonic bacteria which increases stool mass

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16
Q

Butyrate

A

-important energy source for colonocytes (60-70% of energy required)
-important for barrier function and gut integrity
-some is taken up by the liver and oxidized to acetyl-CoA

17
Q

Proprionate

A

-taken up by the liver, metabolized to succinyl-CoA then to TCA intermediates or used for gluconeogenesis

18
Q

Colon Fermentation and pH

A

-lowers the pH
-affects bacterial metabolism and growth

19
Q

Fermentation of nondigestible CHO in the colon

A

-variable extent which nondigestible carbohydrates can be used by colonic bacteria
>minimal use of cellulose
>good use of resistant starch, oligosaccharides, undigested disaccharides

20
Q

Branched chain SCFA

A

-derived from fermentation of the branched chain amino acids by Bacteroides and Clostridium genera

21
Q

Fermentation environment in colon/cecum

A

-anaerobic
-highest concentration of microbes in proximal large intestines

22
Q

Fermentation pathways for synthesis of SCFA

A

1.Breakdown of fermentable poly or oligosaccharides to monosaccharides by bacterial glycosidases
2.Mainly use glycolytic pathway, but no ETC
*energy output relatively low

23
Q

Acetate formation

A

-produced directly from acetyl-coA or via Wood Ljundahl pathway using CO2 (released from pyruvate) as an electron acceptor
-methanogens use the H2 to produce methane

24
Q

Butyrate formation

A

-2 acetyl coA are condensed to form butyryl CoA which is then converted to butyric acid
-converted to B-hydroxybutyrate (ketone)

25
Q

Propionate formation

A

-succinate decarboxylated to propionate by bacteria
>selenomnas ruminantium
>Bacteroides succinogens
-lactate to propionate via acryl CoA

26
Q

SCFA-producing bacteria families

A

-Streptococcaceae
-enterococcaceae
-bifidobacteriaceae
-lactobacillaceae
-clostridiaceae
-prevotellaceae
-enterobacteriaceae
-ruminococcaceae

27
Q

Absorption of volatile fatty acids (VFA)

A

-absorbed through SCFA/HCO3- exchanger active transport, driven by H+, Na+, or just facilitative diffusion
-non-ionized SCFAs are freely absorbed BUT the ionization depends on the VFA pKa and the colon pH

28
Q

Usage of VFAs

A

-Acetate transported through portal vein and goes to liver and periphery
>forms acetyl-coA which will eventually be used in CAC and fatty acid synthesis

29
Q

Proprionate (and lactate) metabolized in hepatocytes

A

> proprionate converted to oxaloacetate then glucose
lactate converted to pyruvate then to glucose

30
Q

Butyrate metabolized by colonic mucosa as energy source

A

> used to make ketone body (beta-hydroxybutyrate in colonocytes for energy
also used as carbon skeleton for fatty acids in milk

31
Q

SCFAs in colon

A

-leads to activation of SCFA G-protein coupled receptors (FFAR2 and FFAR3) which are expressed by L-cells in various tissues
>L-cells secrete GLP-1 and PYY, leads to reduced inflammation and improved barrier function
-Also alter gut microbial composition and activity which may improve gut barrier/immune function

32
Q

Prebiotics

A

-increase growth of specific colon bacteria

33
Q

SCFA as signalling molecules

A

-influence gut-brain communication and brain directly or indirectly
*can cross blood brain barrier
-intestinal barrier function and immunity
-hormone production
-activates brown adipose tissue, regulation of mitochondrial function, increased insulin secretion, whole body energy homeostasis
-systemic inflammation