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digestive performance
of laying hens
A lgae are being increasingly
explored for their nutritional,
structural and biological
properties. For 20 years, Olmix has
show a phylogenetic similarity with
polysaccharides from the animal
kingdom (such as heparin), explain-
ing the unique biological activities
developed marine biotechnology of MSP. Their reactivity, hence their
for animal care, specialising in the biological properties, varies a lot
identification, characterisation and according to the type of sugars and
extraction of specific Marine linkage they contain, their level of
Sulphated Polysaccharides (MSP) sulphation and also their molecular
from green, red and brown algae. weight. Therefore, several MSP with
Among them, a type of MSP with distinct biological activities can be
anti-hyperlipidemic properties was found in algae.
identified and is being used in poul-
try production for its capacity to
stimulate digestion, thanks to its Biological activities of MSP
action on the bile acid cycle and Fig. 1. Marine sulphated polysaccharide (MSP) structure.
lipid metabolism. The different biological activities of
MSP (among others immune-modu-
lating, antioxidant and intestinal liver that lead to the synthesis of As a consequence, the reabsorp-
by Marie Gallissot, Technical mucin production stimulating) have specific molecules involved in the tion of bile acids in the intestine is
Service Manager, Olmix. been studied in recent years. bile acid metabolism. limited and the excretion of bile
www.olmix.com Current scientific publications acids in the faeces is enhanced.
have shown that some MSP have a From its action in the liver, the
direct impact on liver function. Excretion of bile acids FXR also decreases the synthesis of
Macroalgae, or seaweeds, are These new MSP have anti-hyper- PreVLDL (very low density lipopro-
eukaryotic and pluricellular organ- lipidemic properties which regulate The main effect of FXRs in the liver teins), a precursor of cholesterol
isms. They contain a variable part of the cycle of bile acids and the lipid is to favour the excretion of bile transporters, and increases its pas-
carbohydrates (mainly polysaccha- metabolism. acids from the liver to the bile duct. sage into the blood in the form of
rides), proteins, minerals, lipids and Bile acid and lipid metabolism in The bile acids are further trans- VLDL. In the blood, the transforma-
vitamins. the liver and the intestine rely on ported to the intestine, where they tion of VLDL to LDL (low density
The specificity of MSP stands in complex biochemical signalling play a key role in the digestion of lipoproteins) and then HDL (high
the complexity of their structure pathways, being the activation of a fat, by forming micelles with dietary density lipoproteins) is favoured.
(Fig. 1). Indeed, MSP are branched specific nuclear receptor, the lipids, thus making possible the Contrary to LDL, HDL bring back
hetero-polysaccharides, meaning Farnesoid X Receptor (FXR), the ini- digestion of fat by lipase. cholesterol from peripheral organs
that they have 3D structure and are tial point of these metabolic path- The absorption of bile acids in the to the liver, and so the cholesterol
composed of various sugar units ways. Present both in hepatocytes ileum relies on specific transporters, they transport is more easily detoxi-
(including rare ones like rhamnose). and enterocytes, the FXR upregu- whose synthesis is also downregu- fied via the bile acids cycle.
Moreover, these sugars can be sul- lates and/or downregulates the lated by the FXR to prevent any The capacity of algal polysaccha-
phated, conferring them a special activity of several enzymes and the liver injury caused by an overload of rides to improve liver metabolism
reactivity. All these parameters expression of several genes in the bile acids. Continued on page 18
Fig. 2. Effect of various green algae MSP: ulvan extracts (UE) on inhibiting Fig. 3. Effect of different ulvan extracts (UE) on FXR mRNA expression in
pathological changes in the liver, in comparison with negative control the livers of male rats. 1: normal control group; 2: hyperlipidemia group;
and positive control (inositol niacinate). Scoring: mild = 1, moderate = 2, 3: UE1 (250mg/kg); 4: UE2 (125mg/kg); 5: UE2 (250mg/kg); 6: UE2 (500mg/
severe = 3. Different alphabets are significantly different (p<0.05 by one- kg); 7: positive control (cholestyramine, 500 mg/kg). Adapted from Qi et
way ANOVA). Adapted from Pengzhan et al., 2003. al., 2015.
3.0 8
FXR mRNA expression
Score of pathological
7
(hyperlipidemia %)
2.5
6
2.0 a
5
changes
b
1.5 c 4
c
1.0 c 3
2
0.5 1
0 0
Negative UE1 UE2 UE3 Inositol 1 2 3 4 5 6 7
control niacinate
Fig. 4. LDH and AST serum levels before and after DigestSea administra-
tion (IU/L).