Faecal characteristics are important parameters for dog breeders and owners to assess diet quality and also digestibility. Various factors such as the source, amount, and quality of starches, proteins, fibres and minerals can affect the digestibility of dry-expanded diets(Reference Nery, Biourge and Tournier1). Among these factors, starch digestibility is the most sensitive to extrusion processing. Currently available in vitro methods to assess starch gelatinisation in a complex matrix are unreliable(Reference Baks, Ngene and van Soest2). Reports from the field and work in our laboratory have indicated that large breed dogs (>25 kg) are at a higher risk of exhibiting softer and moister faeces than smaller dogs(Reference Weber, Martin and Biourge3).
Starch represents 20–50 % of dry-extruded diets. Among the nutrients, starch has one of the widest variabilities in terms of digestibility and the flow of undigested material into the colon. Resistant starch (RS) has been defined as ‘the sum of starch and starch degradation products not absorbed in the small intestine of healthy individuals’(Reference Champ, Langkilde and Brouns4). Starch can be intrinsically resistant depending on its structure. However, starch resistance also can result from configurational changes during the processing or cooling of cooked starch (retrogradation)(Reference Champ, Langkilde and Brouns4).
The metabolic effects and potential health benefits of RS have been studied extensively in human subjects(Reference Champ, Langkilde and Brouns5). However, few studies(Reference Murray, Fahey and Merchen6, Reference Gajda, Flickinger and Grieshop7) have addressed the effects of RS on the canine colonic ecosystem and faecal quality. To our knowledge, no study has assessed the relationship between RS effects and dog characteristics such as breed and size. Accordingly, the aim of the present study was to assess the effects of various amounts of RS on the faecal scores of dogs differing in breed and size.
Materials and methods
Animals
A total of twenty-one adult female dogs (6·5 (sd 1·5) years) were used in the present study: six miniature poodles (5·0 (sd 1·0) kg body weight); six miniature schnauzers (6·9 (sd 0·5) kg body weight); three giant schnauzers (30·5 (sd 3·5) kg body weight); six German shepherds (27·3 (sd 3·3) kg body weight). The study took place in the Nutrition and Endocrinology Unit of the National College of Veterinary Medicine, Food Science and Engineering, Nantes, France (Oniris). The dogs were housed individually or in groups (with two to three animals of the same breed) in closed indoor/outdoor enclosures. The experimental protocol adhered to the European Union guidelines and was approved by the Animal Use and Care Advisory Committee of Nantes Veterinary School. The protocol was reviewed and approved by the Royal Canin Ethics Committee.
Basal diet
The basal diet was a commercial diet intended for dog maintenance, consisting of 43·0 % total starch (TS; from maize meal), 26·7 % protein, 14·9 % fat and 6·9 % total dietary fibre, DM basis (Royal Canin Adult, Aimargues, France). This diet contained 0·6 % RS, assayed as described below. Each dog was fed an amount previously determined to maintain the optimal body weight (602·4 (sd 25·1) kJ/kg body weight0·75 per d). Free access to water was available at all times. In the present study, all nutrient concentrations are expressed on a DM basis.
Resistant starch supplementations
Using different RS supplementations, three studies were performed over a 3-month period. We used two sources of starch to adjust the RS content in tested diets: high-amylose maize starch (MS; Hi-Maize 260; National Starch, Bridgewater, NJ, USA), wherein TS and RS contents were 94·6 and 42·9 % DM, respectively; potato starch flour (PS; Roquette, Lestrem, France), wherein TS and RS contents were 96·9 and 72·8 % DM, respectively. Studies 1 and 2 intended to assess the effects of increasing amounts of RS. In study 1, MS was added to the basal diet so that the RS content (MS-RS, RS from maize starch) was 0·6, 2·5, 4·3 and 7·4 % DM (addition of 0, 5, 10 or 20 % (w/w) MS, respectively). All dogs were used in this study. In study 2, PS was added to the basal diet in order to increase the RS content (PS-RS) up to 11·4 % DM (addition of 20 % (w/w) PS). Study 3 intended to compare the effects of similar amounts of the two RS. In this study, supplemented diet with PS was only tested on German shepherds. The RS content (PS-TS) was 7·4 % DM. It resulted from 11·1 % (w/w) PS addition to the basal diet. This RS amount was the same as that provided by the highest MS addition in study 1. Results of both these studies were compared together.
Experimental design
All diets were tested successively in all dogs over a 7 d period followed by a 7 d washout period.
Measurements
The TS and RS contents in the supplements were measured with the ‘TS’ and ‘RS’ enzymatic kits (Megazyme, Wicklow, Ireland). The TS kit measured glucose products following complete hydrolysis of the starch by a thermostable α-amylase and amyloglucosidase. The RS kit measured starch digestion by glucose analysis after digestion for 16 h at 37°C in a shaking water-bath with pancreatic α-amylase and amyloglucosidase.
For each period, all stools were scored individually using a faecal score ranging from 1 (hard, dry and crumbly stool) to 5 (liquid diarrhoea). Then, they were classified into three categories: ‘optimal’, defined by a faecal score of 2·5 (well-formed stool, firm and sticky to touch) to 3 (moist-formed stool leaving a definite mark on the floor when picked up); ‘acceptable’, defined by a score of 3–3·75 (most stools have no form and poor consistency); or ‘unacceptable’, defined by a score ≥ 3·75. No faecal score was < 2·5. All individual faeces produced by dogs of the same breed over a 7 d period were used to evaluate the frequency of each score range.
Statistical analysis
Results are presented as the percentage of each score range for each supplementation type and level. Statistical analyses were performed using Statistica 8.0 software (StatSoft, Inc., Tulsa, OK, USA) with the McNemar (χ2) test to compare the frequency of the ‘optimal’ range with and without supplementation. A P value < 0·05 was considered significant.
Results
Study 1 (four breeds; basal, 2·5, 4·3 and 7·4 % resistant starch from high-amylose maize starch)
Smaller dogs (miniature poodles and miniature schnauzers) fed the basal diet (0·6 % RS) presented no unacceptable stools. Faeces were always well formed, with an optimal score frequency of >90 %. In larger dogs, stools with a poor consistency were observed. The frequency of unacceptable scores was 8·5 and 12·1 % in giant schnauzers and German shepherds, respectively.
Regardless of the MS supplementation level (2·5–7·4 % RS), the faecal scores were always optimal in miniature schnauzers (Fig. 1). In miniature poodles, unacceptable scores (6·6 %) appeared with the 4·3 % MS-RS diet. When miniature poodles were fed a 7·4 % MS-RS diet, the frequencies of optimal, acceptable and unacceptable scores were 66·0 , 18·7 and 15·3 %, respectively.
In giant schnauzers and German shepherds, the frequency of unacceptable soft stools was strongly linked to the level of starch added to the diet. Compared with the unsupplemented diet, the quantity of unacceptable scores was doubled (P < 0·0001) with the 2·5 % MS-RS diet (20·0 % frequency in giant schnauzers and 24·1 % frequency in German shepherds). With 4·3 % MS-RS, optimal scores represented < 42·6 % of all scores. Only 15·0 % of faecal scores were optimal among German shepherds fed a diet with 7·4 % MS-RS, while 33·3 % were unacceptable. Feeding with the 7·4 % MS-RS diet was discontinued in giant schnauzers due to very poor faecal quality (i.e. diarrhoea) and the presence of fresh blood and mucus in the stools.
Study 2 (three breeds; 11·4 % resistant starch from potato starch)
When fed the 11·4 % PS-RS diet, the miniature poodles and miniature schnauzers presented well-formed stools with optimal score frequencies of 92·1 and 85 %, respectively. In contrast, the frequency of optimal scores among German shepherds was only 2·2 %, whereas the frequency of unacceptable scores was as high as 89·1 %.
Study 3 (German shepherds; 7·4 % resistant starch from potato starch)
When the 7·4 % PS-RS diet was given to German shepherds, the frequency of unacceptable scores was 75·0 %. This frequency was only 33·3 % when the same amount of RS was provided by MS supplementation (7·4 % MS-RS in study 1).
Discussion
The results of the present study show that dogs respond to indigestible starch differently depending on the size and/or breed. Surprisingly, faecal scores were affected minimally in small breeds (miniature schnauzers and poodles) at all levels of RS supplementation. In contrast, the proportion of unacceptable stools was high even at the lowest level (2·5 % RS) of supplementation in large breed dogs (giant schnauzers and German shepherds). In giant schnauzers fed a diet supplemented with 7·4 % MS-RS, the study had to be discontinued due to signs of colitis (presence of blood and mucus in the faeces), a common complication of excessive carbohydrate fermentation in the colon. This difference in response between small and large dogs was observed with both sources of RS, MS and PS (Fig. 1).
The higher sensitivity of large dogs to RS confirms our previous finding that large dogs fed the same diet at the same energy allowance per kg metabolic body weight present softer and moister faeces than small dogs(Reference Weber, Martin and Biourge3, Reference Hernot, Biourge and Martin8). When the dogs of the present study were fed the commercial unsupplemented diet (study 1), only large dogs presented any unacceptable faecal scores. Large dogs also have been shown to be more sensitive to undigested proteins than small dogs(Reference Nery, Biourge and Tournier1). Although the reason for the higher frequency of lower consistency and moister faeces in large breed dogs remains unclear, it may be explained in part by a longer colonic transit time, higher colonic permeability, proportionally larger colonic volume or higher colonic fermentative activity(Reference Weber, Hernot and Nguyen9Reference Hernot, Dumon and Biourge–Reference Hernot, Nery and Biourge11). Alternatively, this result could be related to the nature of the undigested residues escaping from the small intestine and their predisposition to ferment. These residues might be able to generate greater biomass and fermentation, leading to higher osmotic pressure and higher water content in the stool.
While RS supplementation was similar (7·4 % RS) with MS-RS (study 1) or PS-RS (study 3), faecal quality was much lower with PS supplementation. This observation suggests that, as reported previously, PS induces a higher microflora activity than MS(Reference Bednar, Patil and Murray12). PS is composed of 60 % amylopectin and its enzymatic resistance is conferred by a B-type crystalline form(Reference Englyst, Kingman and Cummings13, Reference Gallant, Bouchet and Buleon14). The MS used in the present study was composed of >70 % amylose. The smaller molecule of glucose units has less area for enzymatic activity(Reference O'Dea, Nestel and Antonoff15) and its glucose units are more active in hydrogen bonding than amylopectin(Reference Thorne, Thompson and Jenkins16). These differences in starch structure also could be responsible for differences in digestion kinetics or utilisation by the microflora of the dog.
The extrusion processing settings (temperature, steam incorporation, pressure and duration), recipe composition (proportion of starch, protein and fat) and starch source affect the outcome of starch cooking by modulating the molecular changes in granular structure that induce loss of crystallinity(Reference Dust, Gajda and Flickinger17). As a result, these parameters affect the RS content in the dry-expanded diet(Reference Murray, Flickinger and Patil18). Starch processing in complex matrices such as dry-expanded diets is not assessed easily by laboratory methods(Reference Nery, Biourge and Tournier1). In vivo tests, although longer and more expensive, are the most appropriate method to determine the response of the dog directly.
Given the relatively high digestive tolerance of miniature schnauzer and poodle dogs despite the high RS concentration used in the present study (11·4 % of measured RS), it appears that small breed dogs would not be good in vivo models to predict starch digestibility and cooking. To our knowledge, the low sensitivity of small dogs to RS has not been reported previously. Further studies are necessary to better understand this phenomenon. In contrast, German shepherd dogs seem to be a good model to discriminate starch cooking and to validate diet processing for dogs in general and for sensitive dogs in particular.
To simulate RS quantities that might be present in commercial diets, supplementations with MS and PS were chosen in the present study, with the final RS supplementation ranging 2·5–11·4 %, as measured by an RS kit. Nevertheless, we cannot exclude that these RS concentrations could not be representative of starch digestibility in the small intestine of dogs and, therefore, would not be a good predictor of faecal quality.
Indeed, principle of the assay method used in the study was originally developed by Englyst et al. (Reference Englyst, Kingman and Cummings13) who used a combination of pancreatin, invertase and amyloglucosidase. This method was amended by McCleary et al. (Reference McCleary, McNally and Rossiter19), who suggested the use of pancreatic amylase and bacterial amyloglucosidase. In addition, the results were correlated with those previously obtained in ileostomised human subjects(Reference McCleary and Monaghan20). This verification ensured that the RS content assessed according to McCleary et al. is representative of ‘starch resistance’ in the human small intestine. We used the same method in the present study, even though the intestinal physiology of dogs is not similar to that of humans (carnivore v. omnivore). Therefore, it can be hypothesised that humans and dogs would not digest starch with the same efficiency. The assay method might be unrepresentative of the ileal digestibility in dogs and the measured RS quantities might be different from those actually entering into the colon.
Moreover, the digestive physiology and efficiency vary depending on age(Reference Meyer and Kienzle21), dietary habits and, as we have shown, on size or breed(Reference Weber, Martin and Biourge3). Thus, the RS levels might be different between dogs. This possibility could explain the different responses observed in the present study between small and large animals.
In conclusion, the present study confirms our previous findings that large dogs pass softer faeces than small dogs when fed the same diet. Based on our previous work, this observation might be linked in part to the higher colonic fermentative activity of large dogs. Surprisingly, the faecal score of small dogs was quite insensitive to RS supplementation, leading us to question the relevance of RS measurement. We conclude that small dogs appear to be poor models for assessing the effects of processing on starch ileal digestibility. The present results also strongly suggest that low indigestible starch content (affected by source and process) is an important factor for ensuring optimal faecal score in large breed dogs.
Acknowledgements
We are grateful to Samuel Ninet (National College of Veterinary Medicine, Food Science and Engineering, Nutrition and Endocrinology Unit, Nantes) and his team for their excellent technical assistance. The present study was supported by a grant from Royal Canin SAS, Aimargues, France. R. G. and M. W. designed and supervised the study. P. N. and V. B. provided administrative, technical and material support. R. G. performed the animal experiments and contributed to the analysis of the data and interpretation of the results. R. G. and M. W. wrote the draft of the manuscript. R. G., M. W., V. B. and P. N. critically reviewed the manuscript. V. B. and M. W. were Royal Canin associates.