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Butyrate and Its Multifarious Effects
Butyrate and Its Multifarious Effects
Butyrate is a short chain fatty acid and an essential energy source for cells in the intestinal tract. However it also
benefits the immune system of animals and holds antibacterial activity. Supplementing diets with coated
butyrate can therefore be beneficial to promote animal health.
Energy supply to intestinal epithelial cells is important due to the fact that the mammalian intestinal mucosa is
one of the most rapidly replicating tissues in the body. For example, studies in rodents demonstrate that the
small intestinal epithelium is completely replaced every two to three days. Thereby, the colonic epithelium is
permanently in close association with microbes and their product, meaning there is a constant immunological
challenge. This makes the barrier defence function of the epithelial layer of great importance. Butyrate is seen
as the most important energy source for intestinal epithelial cells and numerous studies indicate the importance
of butyrate in sodium and water absorption, influence on epithelial cell proliferation and differentiation, villi
development and in improving gut defence systems. In addition, butyrate strengths the barrier function, has
antimicrobial potency and positively influences the immune system. In this article we highlight some of the
documented effects of butyrate and the need for extra supplementation in animal (pet) diets.
Production of butyrate
Butyrate is naturally present in the colon as a result of microbial fermentation of dietary fibre. It is formed by
colon bacteria such as Clostridium, Eubacterium and Butyrivibrio, that ferment the fibres in short-chain fatty
acids (SCFA's), such as acetate, propionate and butyrate. The colon is able to ferment dietary fibre into butyrate
at very high concentrations. Whereas most other cell types utilise glucose as their primary energy source,
colonocytes (colonic epithelial cells) have a great capacity to rapidly metabolise butyrate into energy for the
animal. In the small intestine, microbial formation of butyrate is low or absent. Nevertheless, cells in the small
intestine also express the transporter to bring butyrate into the cells, as shown in a study from 2006. Healthy
growing piglets that were fed butyrate demonstrated that targeting butyrate into the small intestine improves
villi development, gut morphology and function. You can say that the synthesis of many key components of the
intestinal epithelial tissue depends on butyrate metabolism. Only small quantities of butyrate will reach the
general peripheral blood circulation and liver.
Multifarious effects
Butyrate not only provides energy to cells, it also shows many beneficial 'side effects'. For example, in contrast
to the trophic effect on normal healthy colonocytes, butyrate decreases proliferation and differentiation of tutor
cell lines and can finally induce apoptosis; programmed cell death. Butyrate has the ability to influence the gene
expression, thereby inducing early apoptosis in cancer cells. Its opposite is seen in normal, healthy cells, where
butyrate activates gene expression for cell proliferation and maturation. Several epidemiological studies support
the protective role of dietary fibre and its breakdown product butyrate against colonic cancer. These
contradictory patterns of butyrate of stimulating cell growth and differentiation of normal cells and apoptosis
(early cell death) of tumour cells, represents the so called 'butyrate paradox'. Butyrate also has a role as an anti-
inflammatory agent, primarily via inhibition of nuclear factor kB (NF-kB) activation in colonic epithelial cells.
NF-kB regulates many cellular genes involved in early inflammatory responses. The activity of NF-kB is
frequently deregulated in colon cancer and in inflammatory bowel diseases (IBDs). Clinical studies show
beneficial effects of butyrate administration, directly or via dietary fibre, on inflammation and symptoms in
patients with ulcerative colitis (UC, form of IBD). It has been demonstrated that supplemented butyrate is
effective in the treatment of mild to moderate Crohn's disease. A daily dose of oral butyrate resulted in
reduction of the clinical signs and inflammatory parameters in the large intestine. Finally as major precursor for
de novo lipids synthesis used for the cell membrane, butyrate contributes the maintenance of barrier and
transporter functions of the gut. Especially for butyrate there are indications that it increases the defence barrier
of the colon mucosa by stimulation of the formation of mucin glycoproteins. These mucin glycoproteins are
essential in the mucus layer which protects the intestinal epithelium. Studies showed an important role of
butyrate in intestinal wound healing through its positive effect on the tight junctions and gut integrity.
Antimicrobial activity
Extensive use of antibiotics leads to the emergence of antimicrobial resistance, which is not only an issue in
livestock, but also in pet animals. Companion animals are in close contact with humans which increase the risk
on zoonotic transmission, moreover, difficult to treat infections, use of antimicrobials which are also important
in human medicine and limited control on antibiotic treatments increase concerns for public health. Groups of
opportunistic pathogens in pet animals include staphylococci, enterococci, Escherichia coli and Salmonella.
Antimicrobial peptides (like defensins and cathelicidins) are essential effector molecules of the innate immune
system and are of great importance in bacterial host defence. These peptides, also mentioned host defence
peptides (HDP's), possess broad-spectrum antimicrobial activities against bacteria, protozoa, enveloped viruses
and fungi. HDP's can bind to different types of microbial membranes, cause membrane disruption which results
in microbial death. This first line of defence and their natural broad-spectrum against microbes, makes the up
regulation of HDP's an interesting approach as alternative or adjunct therapy to antibiotic treatment.
A recent study revealed a novel role for butyrate in the host defence system. Results from this study in chickens
showed that butyrate increases the antibacterial activity of host immune cells by up-regulation of an array of
HDP's in vitro and in vivo. This immune defence was coupled with a minimum impact on immune cell
activation and inflammation. More importantly, oral supplementation of butyrate resulted in a significant
reduction of Salmonella enteritidis after infection. Same results of butyrate were seen in other studies in
mammals. After antibiotic treatment of Shigella-infected patients, adjunct therapy of sodium butyrate
significantly increased the expression of a specific HDP (cathelicidin LL-37) in the rectal epithelium.
Accompanied by early improvement of rectal inflammation and reduction of pro-inflammatory cytokines in the
stool compared to the control group. Oral butyrate treatment in Shigella infected rabbits resulted in reduced
clinical illness, less severity of inflammation in the colon, significant up-regulation of antimicrobials (HDP's) in
the gut and early reduction of Shigella count in the faeces. Another mechanistic explanation on the
antimicrobial efficacy of butyrate is discussed by the research group of Van Immerseel (2006). An early step in
the pathogenesis of bacteria, like Salmonella, is the interaction between the bacteria and host cells. At low doses
butyrate down regulates expression of invasion genes in Salmonella, thereby reducing the ability of the bacteria
to attach to host cells of the intestinal epithelium, becoming invasive and virulent. Other studies confirm the
efficacy butyrate on inhibition of pathogen colonisation of E. coli and in particular Salmonella.
Studies in swine and chickens showed that coated butyrate is superior to uncoated butyric acid in reducing
intestinal Salmonella colonisation. Environmental contamination and transmission of Salmonella to other
uninfected animals was reduced in the coated butyrate group. The researchers suggest that uncoated butyrate is
taken up by the cells in the upper digestive tract, whereas coated butyric acid will influence the colonisation of
Salmonella bacteria at the site of the colonisation, i.e., in the gut. In addition to targeted release of SCFA over
the digestive tract, coating reduces the typical unpleasant smell of butyrate. Although preferred by some animal
species, most pet owners do not prefer the smell of butyrate in pet food. Wageningen University tested the
effect of extrusion on odour properties of Excential Butycoat (micro-encapsulated sodium butyrate 30%) in a
commercial dog food formulation. During the extrusion process and after packaging of the kibbles, there was no
clear difference observed in smell between the control diets and diets with the coated butyrate.
Conclusion
Butyrate is essential as an energy source for epithelial cells and vital intestinal function. Diverse beneficial
effects of butyrate on animal health can be achieved by the use of dietary fibres and by direct addition of
butyrate to the diet. Butyrate is an important factor in the development of the gastrointestinal tract, but newborn
animals produce only small quantities of butyrate and the production increases during the development of the
hindgut. So supplementation of milk formula and starter diets with butyrate contribute to enhanced development
of the intestinal mucosa and improvement of digestive processes in neonatal calves and piglets. The use of
coated butyrate may play a role in preventing certain types of diarrhoea in animals and create less odour in pet
stools. Use of proper micro-encapsulated butyrate results in targeted release of the SCFA over the digestive
tract. It also reduced the typical smell of butyrate during production and in the feeding of butyrate containing
diets to pet animals.