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Role of Intestinal Microbiota in Ulcerative Colitis

Role of Intestinal Microbiota in Ulcerative Colitis

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Theoretical part<br />

20<br />

4. Modulation <strong>of</strong> the gut microbiota<br />

on colitis, s<strong>in</strong>ce the non‐digestible carbohydrates should be able to reach the distal part <strong>of</strong> the<br />

colon and stimulate the activity <strong>of</strong> the microbiota <strong>in</strong> this colon region. Production <strong>of</strong> non‐digestible<br />

carbohydrates with high molecular weight may help <strong>in</strong>crease the persistence <strong>of</strong> the compound<br />

lead<strong>in</strong>g to slower fermentation, thus penetrat<strong>in</strong>g prebiotic effect all the way throughout the colon<br />

and not only affect<strong>in</strong>g the microbiota <strong>in</strong> the ascend<strong>in</strong>g region (Vernazza et al., 2006;Rastall, 2007).<br />

Langlands et al. (2004) exam<strong>in</strong>ed the prebiotic effect <strong>of</strong> a mixture <strong>of</strong> <strong>in</strong>ul<strong>in</strong> (DP range 6‐60) and<br />

FOS (DP range 2‐8). The study showed that the mixture could significantly <strong>in</strong>crease the level <strong>of</strong><br />

bifidobacteria and lactobacilli <strong>in</strong> both the ascend<strong>in</strong>g and descend<strong>in</strong>g colon <strong>of</strong> healthy human<br />

subjects. Approaches for slowly fermentation do not only <strong>in</strong>clude high cha<strong>in</strong> length. Rose et al.<br />

(2010) demonstrated that starch‐entrapped microspheres could be used to decrease the<br />

fermentation rate.<br />

The ability <strong>of</strong> non‐digestible carbohydrates to improve the colonic environment is not only<br />

restricted to the properties through fermentation. Other studies have shown that the exogenous<br />

structure <strong>of</strong> specific non‐digestible carbohydrates can affect the presence <strong>of</strong> pathogenic bacteria.<br />

One <strong>of</strong> the features is the ability <strong>of</strong> some prebiotics (e.g. FOS and GOS) to act as a molecular<br />

receptor decoy, which can competitively <strong>in</strong>hibit bacterial adhesion (Kunz et al., 2000;Shoaf et al.,<br />

2006;Gibson et al., 2006). Another feature is the ability <strong>of</strong> prebiotic candidates (e.g. XOS and<br />

cellobiose) to act as a repressor <strong>of</strong> virulence factors by repress<strong>in</strong>g the gene expression <strong>in</strong><br />

enteropathogens such as Listeria monocytogenes (Gilbreth et al., 2004). In addition, a recent <strong>in</strong><br />

vitro study us<strong>in</strong>g Caco2 cells has shown that FOS could <strong>in</strong>itiate an anti‐<strong>in</strong>flammatory response even<br />

<strong>in</strong> the absence <strong>of</strong> <strong>in</strong>test<strong>in</strong>al bacteria by <strong>in</strong>duc<strong>in</strong>g the nuclear receptor PPAR gamma (Zenhom et al.,<br />

2011). Table 3 summarizes the desirable attributes <strong>of</strong> prebiotics.<br />

Table 3: Desirable attributes <strong>of</strong> prebiotics<br />

Action Properties Reference<br />

Colonic fermentation Selectively metabolized by bacteria with (Fooks and Gibson,<br />

health promot<strong>in</strong>g effects<br />

2002;Rastall, 2007)<br />

Persistence through the Reach<strong>in</strong>g both the proximal and to some (Langlands et al., 2004)<br />

colon<br />

extent the distal colon.<br />

Inhibition <strong>of</strong> adhesion Possess<strong>in</strong>g receptor like sequences. (Kunz et al., 2000;Shoaf et al.,<br />

by pathogens<br />

2006;Gibson et al., 2006)<br />

Repression <strong>of</strong><br />

pathogenic bacteria<br />

Down‐regulat<strong>in</strong>g virulence factors. (Gilbreth et al., 2004)<br />

Immune modulation Regulat<strong>in</strong>g anti‐<strong>in</strong>flammatory responses (Zenhom et al., 2011)

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