EDP Sciences Journals List
Free access
Issue Dairy Sci. Technol.
Volume 90, Number 6, November–December 2010
Page(s) 707 - 713
DOI http://dx.doi.org/10.1051/dst/2010025
Published online 18 June 2010

© INRA, EDP Sciences, 2010

1. INTRODUCTION

The milk contains two main nitrogen fractions, the most important part under protein form (casein and whey protein) and a second part under non-protein form representing < 6% of total nitrogen content in cow milk. This non-protein nitrogen (NPN) part includes mainly urea (48% in cow milk). The remaining NPN fraction is composed of amino acids, creatine, hippuric acid, sometimes ammonia, etc. As for the determination of urea in blood (uremia), the urea concentration in milk gives information on the protein status of the animal. Several authors reported positive correlation between uremia and urea in milk [7, 24]. The urea concentration in blood is generally reflected in the milk at 83–98% [15].

If the main nitrogen fractions in camel milk were known and well described in the literature [8, 9], the NPN fractions were rarely specified and their variability never described [1], contrary to cow milk [7]. In a comprehensive study on the variability of camel milk composition in Kazakhstan, including the two species of large camelids (Camelus dromedarius and Camelus bactrianus) and their hybrids, urea was determined in milk samples all over a year [19].

The present communication aims to give some reference values for urea content in camel milk and to explore some interpretable variation factors.

2. MATERIALS AND METHODS

2.1. Sampling procedure

To obtain maximum variability, the camel milk was sampled in four different regions at extreme points of Kazakhstan: Almaty, Atyrau, Aralsk and Shymkent (the maximum distance between the various points was > 3500 km) and in the four seasons of the year. In total, 102 samples were used for quantitative determination of the urea in camel raw milk (Tab. I). Those samples, collected randomly among lactating females on two private farms per region, comprised Bactrian (n = 47), dromedary (n = 34), hybrid (n = 7) and mixed milk (n = 14). Sampling was achieved at the milking time in the morning before starting to pasture. In Kazakhstan, the calving season was short and occurred within < 2 months. Bactrian camel milk samples originated from different Kazakh types as depending on their geographical location: Uralobokeliki, Kyzylorda and Ontustik-Kazakhstan [20, 26]. Milk samples from dromedary camel came from the Turkmen Arvana breed [5, 25]. Hybrid samples involved F1 or F2 crossbred animals. In all cases, milk was obtained by manual milking and kept frozen at −20 °C until analysis.

Table I.

Camel raw milk sampling design by region (Almaty, Atyrau, Aralsk and Shymkent), species and season (W, winter; Sp, spring; Su, summer and A, autumn).

2.2. Laboratory analysis

Urea was analyzed by enzymatic method using kit UV-method (Enzymatic BioAnalysis/Food Analysis, Cat. No. 0 542 946, Boehringer-Mannheim distributed by R-Biopharm France). The principle of the dosage was based on the hydrolysis of the urea into ammonia and carbon dioxide by urease. Then, in the presence of glutamate dehydrogenase and NADH, H+ ion ammonium gave L-glutamate and NAD+. The disappearance of NADH was measured at 334 or 340 nm.

In order to study the correlation with protein content in milk, the total protein content (TPC) was determined: Nitrogen (N) was determined by the Kjeldahl method [16] and the conversion N × 6.38 was used to quantify the TPC.

The main plants consumed by the camels were sampled in spring and the protein content was also determined by the Kjeldahl method.

2.3. Statistical analysis

A linear model was tested for urea concentration as dependent variables. The tested variation factors were the region (Reg), the species (Spec), the season (Seas) and their interactions. The limit of signification level for variance analysis was 0.05. The results are presented as mean plus/minus standard error. As the variances were not homogeneous, data were log transformed in order to get normal distribution of the values (log transformation). The correlation between NPN and TPC was tested using Pearson correlation. The software used was XLStat2009.

3. RESULTS AND DISCUSSION

The non-protein fraction determination in cow’s milk is useful for the cheese industry [15], for assessment of the potential nitrogen pollution by dairy cows [6], as indicator for the reproduction performances control [14] and for assessing feeding strategy of dairy animals [2]. This last point is particularly important in dairy cow farming systems, because the milk urea determination could improve the general metabolic efficiency of the producing animal, but could also help for a better economical management by reducing the protein overfeeding in the diet. However, the use of camel milk is not common in cheese industry, and the contamination risk for environment is low in extensive farming system. Nevertheless, the present trends were dairy intensification in camel farming system which requires a more convenient feeding management. In that context, the determination of milk urea takes a new importance as indicator of protein feeding [18]. Elsewhere, the variability of urea is not referenced in this species.

3.1. Mean value of urea in camel milk

On average, in the 102 camel milk samples, the urea concentration was 81.6 ± 60.4 mg·L−1. Twelve milk samples had no urea. The values were in the range 0–290.5 mg·L−1. Very few references concerning urea in camel milk were reported in the literature. The concentrations in camel milk generally ranged between 80 and 400 mg·L−1 as well in cow [27] as in goat [15, 21] with a recommended average between 100 and 160 mg·L−1 [2]. On average, our values appeared lower with a range between 0 and 290 mg·L−1 and a median of 80 mg·L−1. The nitrogen metabolism was appreciably different in camel where the urea recycling was quite more important than for other ruminants [22]. According to the distribution of the values in our study, the normal level in camel milk could be considered between 30 and 120 mg·L−1. It is quite surprising to find some zero value in urea concentration in milk as no similar observations were reported in cow or goat milk. Generally, the low urea values in milk were encountered in case of limited availability of degradable nitrogen, but in our samples there was no difference in protein concentration between milk with no urea and milk with urea.

3.2. Variation factors

If the variation factors of urea in cow milk were described for long time [17], no data were available for camel milk. The analysis of variance (ANOVA) showed a significant effect of the season (Tab. II) on the urea concentration in milk (P < 0.001). The highest value in camel milk urea was observed in spring (111.5 ± 77.6 mg·L−1) and the lowest in autumn (46.4 ± 38.0 mg·L−1). No significant difference was observed between species or region. However, a significant interaction Season × Region was reported (P < 0.001). The pattern of seasonal change was clearly observed in Shymkent region only. Usually, the main variation factor of urea concentration in milk was the feeding, especially the ratio protein/energy [4]. A high urea concentration in milk could be caused by an excess of proteins degraded in the rumen or an excess of non-degraded proteins in the gut in relation to the available energy for using them [7]. So, the urea concentration in milk could be used as an indicator of the protein overfeeding [13], better than the total protein. However, a high concentration could also show a severe protein underfeeding leading to an important protein catabolism, as it was observed in blood urea of young camel under severe protein deficiency [10].

Table II.

Source of variation (type III) and signification level (test F) for the urea and ammonia concentration in camel milk from different regions of Kazakhstan at different seasons and for different species.

No data were available in our study on the feeding system of the animals, but all of them were fed on natural pastures. The pastures were composed mainly of Artemisia sp. (14.6 ± 5.2%), Alhadji Pseudolhadji (22.7 ± 3.2%) and Tamarix sp. (17.3 ± 2.8%), all plants containing relatively high level of protein. However, the quality of the pasture being linked to the season, the relationship with season was not a surprise. Indeed, the nutritive value of the diet, notably the content in soluble nitrogen, was obviously higher in spring at the beginning of the plant growth after winter time. This nutritive value, especially the protein content of the grasses, decreased with the hot season. The lowest mean value was reported in autumn. In winter, the animals could receive some supplements (hay or concentrates) contributing to an increase of the protein in the diet and correlatively of the urea concentration in milk. In dairy cow, some authors reported a significant increasing of urea in milk at the pasture starting time after indoor housing period in winter [23]. Among the milk samples containing a very high quantity of urea (> 130 mg·L−1), 92% were collected in spring and 75% came from Shymkent region where the food supplementation (concentrates rich in soluble nitrogen) at the end of winter was a common practice. The sensitive response to soluble nitrogen supplementation in camel was a common feature already described. In some cases, it could lead to ureic intoxication [11].

This direct relationship between milk urea and season (i.e. nutritive value of the natural diet) could also explain the relationship with the total protein in milk. Indeed, considering the whole sample, urea concentration in milk was positively correlated to total protein concentration (TPC) in milk (r = 0.308; P < 0.005) (Fig. 1). This parameter was under the same influence as urea, and the highest TPC in camel milk was also observed at spring [19]. The seasonal variation of urea in milk could be also explained partially by the lactation stage. In zero-grazing farming system, the urea in cow milk was low at the beginning of the lactation, then increased after one month of lactation, and decreased at the end of lactation [3]. In our study, the calving season occurred in winter (December to February). The spring corresponded to the lactation peak. So, a mixed effect (lactation stage and nutritive value of the diet) could support the observed seasonal effect.

thumbnail Figure 1.

Correlation and variance ellipse (for 2 SD) between urea concentration in camel milk and total protein in milk in Kazakhstan (n = 95; the samples containing no urea were not represented).

The absence of relationship with the species underlined probably the lack of genetic effect. In dairy cow, the between breed variability was generally lower than the within breed variability [2]. In large camelids, urea did not appear as a discriminant parameter of the milk composition between the species [12].

The regional effect was a combination of feeding and climatic conditions. The significant interaction Season × Region could be partly attributed to the overlapping between seasonal feeding variation and regional feeding variation.

4. CONCLUSION

The NPN fraction (urea) in camel milk represented < 2% of the nitrogen content in our camel milk samples. On average, the urea content in camel milk appeared lower than in cow. The camel is well known for its ability to develop mechanisms of resistance to mineral, energetic or protein underfeeding. The nitrogen recycling is one of these mechanisms, allowing the camel to valorize poor nutritive grasslands. The relative low quantity of urea in milk testifies the ability of camel to limit the urea excretion through the milk. It could be a supplementary asset in the adaptation of camel to the harsh desert conditions. However, in case of food supplementation rich in soluble nitrogen, the quantity of urea can reach high level in milk, reflecting a high level in blood (hyperuremia). In fact, the camel is very sensitive to ureic contamination and the supply in urea, as it is currently proposed for dairy cow, has to be avoided for dairy camel.

Acknowledgments

The study was supported by the French Ministry of Foreign Affairs (ECONET Programme) and by the French Embassy at Almaty (Kazakhstan). We also thank the camel farmers from Kazakhstan where the milk sampling was achieved.

References

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All Tables

Table I.

Camel raw milk sampling design by region (Almaty, Atyrau, Aralsk and Shymkent), species and season (W, winter; Sp, spring; Su, summer and A, autumn).

Table II.

Source of variation (type III) and signification level (test F) for the urea and ammonia concentration in camel milk from different regions of Kazakhstan at different seasons and for different species.

All Figures

thumbnail Figure 1.

Correlation and variance ellipse (for 2 SD) between urea concentration in camel milk and total protein in milk in Kazakhstan (n = 95; the samples containing no urea were not represented).

In the text