Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-03T09:10:23.387Z Has data issue: false hasContentIssue false

Effect of short-chain fructooligosaccharide-enriched energy-restricted diet on weight loss and serum haptoglobin concentration in Beagle dogs

Published online by Cambridge University Press:  12 October 2011

Rebecca Ricci*
Affiliation:
Department of Animal Science, University of Padua, Viale dell'Università 16, 35020Legnaro (Padua), Italy
Isabelle Jeusette
Affiliation:
Affinity-Petcare, Barcelona, Spain
Jean-Marie Godeau
Affiliation:
Biochemistry Unit, Department of Functional Sciences, University of Liege, Liege, Belgium
Barbara Contiero
Affiliation:
Department of Animal Science, University of Padua, Viale dell'Università 16, 35020Legnaro (Padua), Italy
Marianne Diez
Affiliation:
Department of Animal Production, Faculty of Veterinary Medicine, University of Liege, Liege, Belgium
*
*Corresponding author: Dr R. Ricci, fax +39 49 8272669, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

The effects of the dietary inclusion of two levels of short-chain fructooligosaccharides (sc-FOS) on weight loss, biochemical parameters and serum haptoglobin concentration were investigated in twelve experimental obese Beagle dogs. Dogs were randomised into two groups and submitted to a weight loss program (WLP): the control group (C) received a commercial energy-restricted high-protein diet containing 1 % DM sc-FOS, whereas the test group (T) received the same diet enriched with sc-FOS to attain a 3 % DM content. Body weight (BW) and body condition score were weekly assessed in each dog and blood was collected before and after WLP to measure total plasma cholesterol (CHOL), TAG, NEFA, glucose (GLUC), insulin, serum leptin and haptoglobin. Groups showed similar BW and blood parameters before treatment. When values before and after treatment of the dogs were compared, significant reductions were observed for all parameters, with the exception of NEFA and GLUC. However, when these reductions were compared between C and T groups, significant differences were detected only for haptoglobin (T before v. T after: 1545 v. 605 mg/l, P = 0·03; C before v. C after: 1635 v. 1400 mg/l, P = NS). Positive correlations between haptoglobin and CHOL and between haptoglobin and TAG were observed before but not after WLP. In conclusion, feeding obese dogs with the energy-restricted diet caused significant weight loss and reduction of blood parameters, irrespective of the sc-FOS content included. However, serum haptoglobin level, and the subclinical inflammatory condition associated with it, was significantly lowered in the T but not in the C group.

Type
Full Papers
Copyright
Copyright © The Authors 2011

Recent studies have underscored the increased efficiency of obese mice's microbiota in harvesting energy from the diet(Reference Bäckhed, Ding and Wang1, Reference Turnbaugh, Ley and Mahowald2), suggesting that the gut microbial population acts as an environmental factor influencing fat storage and obesity development(Reference Vrieze, Holleman and Zoetendal3). On the basis of these findings, the increased attention recently addressed to the role of dietary fiber on the lipid profile and glucose (GLUC) metabolism of obese dogs seems appropriate, as it has the potential to modulate gut microbiota(Reference Roberfroid4). Short-chain fructooligosaccharides (sc-FOS) are non-viscous β-fructan fibers that enhance a beneficial microbial fermentation in the colon by producing SCFA, mainly acetate and propionate. A series of studies carried out on rodents demonstrated that inulin-type fructans (e.g. inulin and oligofructosaccharides) affect lipid metabolism by lowering serum TAG concentration(Reference Delzenne and Kok5) and, even if to a lesser degree, decreasing serum cholesterol (CHOL)(Reference Beylot6). The suggested mechanisms to explain these effects are related mainly to the decrease of the activity of lipogenic hepatic enzymes and to the production of butyrate, a SCFA that inhibits liver CHOL synthesis(Reference Delzenne, Daubioul and Neyrinck7, Reference Ooi and Liong8). In human subjects, however, results on the effect of inulin-type fructans on lipid metabolism are conflicting. Most of the studies failed to demonstrate a beneficial effect in reducing plasma lipid concentrations in healthy volunteers, whereas hypotriglyceridaemic and/or hypocholesterolaemic effects were achieved in type-2 diabetic and hyperlipidaemic patients; in all studies, the dietary supplementation of either inulin or oligofructosaccharides ranged from 7 to 20 g/d and the time of administration was between 2 and 8 weeks(Reference Beylot6). The variability of the basal diet and the difficulties in controlling the nutrient intake in human subjects may explain, at least in part, the lack of consistent results achieved in human studies(Reference Forcheron and Beylot9). Our hypothesis is that sc-FOS dietary inclusion may influence the metabolism of obese dogs and reduce the inflammatory state due to the chronic overweight condition. To date, no indications are available on the optimal sc-FOS level in the diet to enhance beneficial effects on the metabolism of obese dogs.

In the present study, we therefore investigated the effects of two levels of sc-FOS (1 v. 3 % DM) on weight loss, biochemical parameters and serum haptoglobin in obese dogs. With this aim, a commercial dry energy-restricted diet containing 1 % DM sc-FOS was used as control and supplementary sc-FOS were added to the diet to reach 3 % DM of dietary content.

Experimental methods

The present study was carried out using twelve chronically obese Beagle dogs (six neutered males, three entire females and three neutered females, aged between 3 and 9 years; mean body weight (BW) 21·9 (sem 2·7) kg) with a body condition score of 7 or 8 on a nine-point scale(Reference Laflamme10). Dogs were randomised into two groups of six individuals and submitted to a weekly 1–2 % weight loss program (WLP) until optimal body condition score was obtained. The experimental protocol was approved by the Ethical Committee of the University of Liege, Belgium, before experimentation.

The WLP was implemented using a commercial energy-restricted high-protein extruded diet (as fed: 34 % crude protein, 9·5 % fat and 12 kJ Metabolizable Energy (ME)/g, Obesity Veterinary Diet, Royal Canin, Aimargues, France), which contains 1 % DM sc-FOS, as included by the manufacturer. The control group (C) received the commercial diet only, whereas the test group (T) received the same diet enriched with a sc-FOS supplement (Beghin-Meiji Industrie, Marckolsheim, France) in order to attain a 3 % DM sc-FOS dietary content.

BW and body condition score were weekly assessed for each dog and an individual blood collection was carried out before and after WLP to quantify plasma CHOL, TAG, NEFA, GLUC, insulin, leptin and haptoglobin. Briefly, blood samples were collected in tubes containing K3EDTA as anticoagulant and kept frozen at − 20°C until assayed. Plasma CHOL, TAG and GLUC were analysed by Technicon autoanalyser RA-1000 (Bayer Diagnostics, Holliston, MA, USA) using reagents from Bayer (Leverkusen, Germany), whereas NEFA concentrations were assayed by means of an enzymatic method (NEFA, Half microtest; Roche Diagnostics GmbH, Penzberg, Germany). Insulin plasma concentrations were analysed using a commercial RIA kit (INS-IRMA kit; Biosource Europe, Nivelles, Belgium) and leptin levels were measured using a canine-specific ELISA method validated by Iwase et al. (Reference Iwase, Kimura and Komagome11). An assay was developed at the laboratory of Biochemistry Unit of the Faculty of Veterinary Medicine in Liege in order to measure plasma canine haptoglobin concentration. This is a photometric method that measures the peroxidase activity of the haptoglobin–cyanmethaemoglobin complexes, as described elsewhere(Reference Humblet, Coghe and Lekeux12).

Data were analyzed using PROC GLM of SAS (Statistical Analysis Systems statistical software package version 6.11; SAS Institute, Cary, NC, USA) to initially detect the effect of group (C v. T) and sex (females v. neutered females v. neutered males) on BW and blood parameters measured before WLP. A SPLIT PLOT model using PROC GLM of SAS (SAS Institute) was then adopted to detect the effects of dietary treatment, time (before v. after WLP) and the interaction between dietary treatment and time on BW and all blood parameters of dogs being treated. P values for the multiple comparisons of the interaction effect have been adjusted using the Bonferroni method. Pearson correlation analyses were performed on BW and blood parameters using data measured before and after WLP, with P values < 0·05 considered significant.

Results

All dogs reached body condition score of 5–9 between 21 and 32 weeks (average 26 weeks) and the average BW attained at the end of the WLP was 14·4 (sem 1·1) kg (ranging from 12·7 to 15·8 kg). Before WLP, no differences in BW and blood parameters were detected either among sexes or between treatments; therefore, groups were considered homogenous.

The effects detected in the present study when values before and after the dietary treatment were considered are shown in Table 1. The dietary treatment (1 v. 3 % DM sc-FOS) had a significant influence only on haptoglobin concentration (C group (1518 mg/l) v. T group (1075 mg/l), P < 0·05), whereas time significantly affected dogs' BW, CHOL, TAG, insulin, leptin and haptoglobin, which were significantly lower after WLP; GLUC, on the contrary, was significantly higher and NEFA was unaffected by time. However, when blood parameter reductions after WLP were compared between C and T groups, significant differences were detected only for haptoglobin, as the T group exhibited a significant reduction after WLP, which was not detected in the C group (T before v. T after: 1545 v. 605 mg/l, P = 0·03; C before v. C after: 1635 v. 1400 mg/l, P = NS; Table 2).

Table 1 P values of the effects of dietary treatment (1 v. 3 % DM short-chain fructooligosaccharide), time (before v. after weight loss program) and interaction of dietary treatment and time on body weight (BW) and blood parameters of the dog

(Root mean squared errors (RMSE), goodness of fit (R 2) and coefficients of variations)

CHOL, cholesterol.

Table 2 Body weight (BW) and blood parameters resulting from the interaction between dietary treatment and time in test (T) and control (C) groups

(Estimated least squares mean values and standard error of the difference (SED))

CHOL, cholesterol.

a,b,c Values within a row with unlike superscript letters were significantly different (P < 0·05). P values have been adjusted by Bonferroni test.

* 1 % DM short-chain fructooligosaccharide (sc-FOS).

3 % DM sc-FOS.

The SED shown is the maximal one based on between dog variation and was also used for the multiple comparisons.

Significant positive correlations were observed before WLP between haptoglobin and TAG (0·65, P < 0·05) and between haptoglobin and CHOL (0·78, P < 0·01), but not after WLP (haptoglobin and TAG − 0·15, P = NS and haptoglobin and CHOL 0·07, P = NS).

Discussion

sc-FOS are inulin-type fructans that are hydrolysed and completely fermented by the colonic microflora to produce gases and SCFA. By modulation of the composition of the microflora in the colon, sc-FOS have the potential to improve colonic health and consequently the well-being of the host(Reference Roberfroid4).

The use of a high-protein low-carbohydrate diet has already been demonstrated to be effective in ensuring canine weight loss, minimising lean body mass losses(Reference Diez, Nguyen and Jeusette13) and reducing the level of plasma CHOL and TAG concentrations in obese dogs(Reference Diez, Michaux and Jeusette14). In the present study, the dogs were chronically obese, and the effect of sc-FOS included in an energy-restricted high-protein diet on BW loss and blood parameters was investigated.

A blend of fibers (5 and 10 % DM), including sc-FOS, has already been shown to be efficient in lowering the post-prandial GLUC, urea and TAG concentrations, as well as the pre-prandial concentrations of urea, TAG and CHOL after a 6-week period of administration in a group of healthy dogs(Reference Diez, Hornick and Baldwin15). More recently, the 1 % DM sc-FOS inclusion in a diet aiming to maintain dogs in an obese state decreased insulin resistance, although CHOL and TAG were not affected by the treatment (control diet v. sc-FOS diet: CHOL 5·4 (sem 0·7) v. 5·5 (sem 0·7) mmol/l and TAG 1·4 (sem 0·6) v. 1·5 (sem 0·5) mmol/l)(Reference Respondek, Swanson and Belsito16).

In the present study, a significant reduction of both BW and blood parameters was observed after WLP, and, although GLUC concentration significantly increased, its value was still within the physiological range. Notwithstanding this, we observed that including either 1 % DM or 3 % DM sc-FOS to the energy-restricted diet induced no differences in either BW or biochemical parameters and this may be due to the small difference in the quantity of sc-FOS between the two diets.

Interestingly, when blood parameter values after WLP were compared between C and T groups, haptoglobin was found to be significantly lower in the group receiving 3 % DM sc-FOS.

It is known that obesity promotes a low-grade inflammatory state, and in human subjects, concentrations of haptoglobin and other inflammatory markers have been shown to significantly increase with obesity(Reference De Pergola, Di Roma and Paoli17) and to decrease as a consequence of body fat mass reduction(Reference Belza, Toubro and Stender18). Therefore, recent attention has focused on the measurement of acute phase proteins in canine obesity. German et al. (Reference German, Hervera and Hunter19) demonstrated a significant decrease of haptoglobin and C-reactive protein concentrations in twenty-six obese dogs after weight loss, suggesting a relationship between obesity and a subclinical inflammatory state. On the contrary, a recent study carried out on Beagle dogs failed at demonstrating an increase in haptoglobin and other acute phase protein concentrations after an experimentally induced fattening period(Reference Tvarijonaviciute, Martinez and Gutierrez20); however, authors concluded that this was probably due to the short-term fattening period (10 weeks).

Our results confirm that the obese condition in dogs is characterised by a significantly higher haptoglobin concentration in the blood and they further demonstrate that haptoglobin is positively correlated to the lipaemic profile of the dogs, and particularly to TAG and CHOL concentrations in the blood. Surprisingly, in the present study, haptoglobin concentration before WLP was not correlated to leptin, which is a quantitative marker of adiposity in dogs.

Although the small number of dogs used in the present study certainly represents a limit, however, some conclusions can be drawn. Feeding obese dogs with an energy-restricted high-protein diet caused significant weight loss and reduction of obesity-related biochemical parameters such as TAG, CHOL, insulin and leptin, irrespective of the sc-FOS content in the diet (1 % DM or 3 % DM). Conversely, serum haptoglobin level, and the subclinical inflammatory state associated with it, was significantly lowered only when 3 % DM sc-FOS was included in the diet. Further studies involving a larger population will be needed to investigate the effect of including inulin-type fructans on canine obesity and metabolism.

Acknowledgements

At the time of the study, the authors had no financial or personal relationship with other people or organisations that might inappropriately influence or bias the paper. When the study was being carried out, I. J. was a PhD student of the Nutrition Unit, funded by the University of Liege. Royal Canin provided the dog food and Beghin-Meiji Industrie, the sc-FOS supplement. R. R. collected the clinical data, analysed the results and drafted the paper, I. J. collected the clinical data and reviewed the manuscript, J.-M. G. performed blood analyses, B. C. analysed the results, M. D. designed the study, reviewed the results and reviewed the manuscript. The work was performed at the Department of Animal Production, Faculty of Veterinary Medicine, University of Liege, Boulevard de Colonster, 20 B-4000 Liege, Belgium.

References

1Bäckhed, F, Ding, H, Wang, T, et al. (2004) The gut microbiota as an environmental factor that regulates fat storage. Proc Natl Acad Sci U S A 101, 1571815723.CrossRefGoogle ScholarPubMed
2Turnbaugh, PJ, Ley, RE, Mahowald, MA, et al. (2006) An obesity-associated gut microbiome with increased capacity for energy harvest. Nature 444, 10271031.CrossRefGoogle ScholarPubMed
3Vrieze, A, Holleman, F, Zoetendal, EG, et al. (2010) The environment within: how gut microbiota may influence metabolism and body composition. Diabetologia 53, 606613.Google Scholar
4Roberfroid, MB (2005) Introducing inulin-type fructans. Br J Nutr 93, S13S25.CrossRefGoogle ScholarPubMed
5Delzenne, N & Kok, N (1999) Biochemical basis of oligofructose-induced hypolipidemia in animal models. J Nutr 129, 1467S1470S.CrossRefGoogle ScholarPubMed
6Beylot, M (2005) Effects of inulin-type fructans on lipid metabolism in man and animal models. Br J Nutr 93, S163S168.CrossRefGoogle Scholar
7Delzenne, NM, Daubioul, C, Neyrinck, A, et al. (2002) Inulin and oligofructose modulate lipid metabolism in animals: review of biochemical events and future prospects. Br J Nutr 87, S255S259.Google Scholar
8Ooi, LG & Liong, MT (2010) Cholesterol-lowering effects of probiotics and prebiotics: a review of in vivo and in vitro findings. Int J Mol Sci 11, 24992522.Google Scholar
9Forcheron, F & Beylot, M (2007) Long-term administration of inulin-type fructans has no significant lipid-lowering effect in normolipidemic humans. Metabolism 56, 10931098.Google Scholar
10Laflamme, DP (1997) Development and validation of a body condition score system for dogs. Canine Pract 22, 1015.Google Scholar
11Iwase, M, Kimura, K, Komagome, R, et al. (2000) Sandwich enzyme-linked immunosorbent assay of canine leptin. J Vet Med Sci 62, 207209.CrossRefGoogle ScholarPubMed
12Humblet, M, Coghe, J, Lekeux, P, et al. (2004) Acute phase proteins assessment for an early selection of treatments in growing calves suffering from bronchopneumonia under field conditions. Res Vet Sci 77, 4147.Google Scholar
13Diez, M, Nguyen, P, Jeusette, I, et al. (2002) Weight loss in obese dogs: evaluation of a high-protein, low-carbohydrate diet. J Nutr 132, 1685S1687S.CrossRefGoogle ScholarPubMed
14Diez, M, Michaux, C, Jeusette, I, et al. (2004) Evolution of blood parameters during weight loss in experimental obese Beagle dogs. J Anim Physiol Anim Nutr 88, 166171.Google Scholar
15Diez, M, Hornick, JL, Baldwin, P, et al. (1997) Influence of a blend of fructo-oligosaccharides and sugar beet fiber on nutrient digestibility and plasma metabolite concentrations in healthy Beagles. Am J Vet Res 58, 12381242.CrossRefGoogle ScholarPubMed
16Respondek, F, Swanson, KS, Belsito, KR, et al. (2008) Short-chain fructooligosaccharides influence insulin sensitivity and gene expression of fat tissue in obese dogs. J Nutr 138, 17121718.CrossRefGoogle ScholarPubMed
17De Pergola, G, Di Roma, P, Paoli, G, et al. (2007) Haptoglobin serum levels are independently associated with insulinemia in overweight and obese women. J Endocrinol Invest 30, 399403.CrossRefGoogle ScholarPubMed
18Belza, A, Toubro, S, Stender, S, et al. (2009) Effect of diet-induced energy deficit and body fat reduction on high-sensitive CRP and other inflammatory markers in obese subjects. Int J Obes 33, 456464.Google Scholar
19German, AJ, Hervera, M, Hunter, L, et al. (2009) Improvement in insulin resistance and reduction in plasma inflammatory adipokines after weight loss in obese dogs. Domest Anim Endocrinol 37, 214226.CrossRefGoogle ScholarPubMed
20Tvarijonaviciute, A, Martinez, S, Gutierrez, A, et al. (2011) Serum acute phase proteins concentrations in dogs during experimentally short-term induced overweight. A preliminary study. Res Vet Sci 90, 3134.Google Scholar
Figure 0

Table 1 P values of the effects of dietary treatment (1 v. 3 % DM short-chain fructooligosaccharide), time (before v. after weight loss program) and interaction of dietary treatment and time on body weight (BW) and blood parameters of the dog(Root mean squared errors (RMSE), goodness of fit (R2) and coefficients of variations)

Figure 1

Table 2 Body weight (BW) and blood parameters resulting from the interaction between dietary treatment and time in test (T) and control (C) groups(Estimated least squares mean values and standard error of the difference (SED))