Energy intake and milk production were measured in 12 mink dams raising litters of 3, 6 and 9 kits one to four weeks post partum by means of balance experiments and measurements of milk intake of the kits by the water isotope dilution technique. The dams were fed ad libitum on a conventional wet mink diet (DM: 323 g/kg; CP: 173 g/kg; ME: 4.4 MJ/kg). Milk samples collected from dams with corresponding litter sizes and lactation weeks, and body composition of kits nursed by these dams, were analysed for content of DM, ash, N and fat. The ME and drinking water consumption were higher in dams nursing 9 kits than in dams nursing 3 kits. The N and water balances as well as the live weight of dams were not affected by litter size. Daily milk production was higher in dams nursing 9 kits than in dams nursing 3 kits. The DM, N and fat content of the milk increased during lactation, but were not affected by litter size. Individual kit live weight was higher in litters of 3 than in litters of 6 and 9 kits four weeks post partum. The DM and fat content of the kits were lowest in kits from litters of 9 kits, whereas these kits had the highest protein content. Daily ME for maintenance of kits and the efficiency of utilisation of ME in milk for body gain were estimated to 356 kJ/kg0.75, kp approximately 0.53 and kf approximately 0.71, respectively. In conclusion, daily milk production increased with increasing litter size, but not in proportion to the number of kits, indicating that milk production limits the growth rate of the young. In the fourth week of lactation, milk production was not different between dams nursing 6 or 9 kits, indicating a maximum capacity.
Thirty mink dams nursing litters of 6 kits were assigned to one of 3 dietary treatments to investigate the effects of changing the protein:carbohydrate ratio on nutrient utilization, heat production, milk production and kit growth. Three diets were formulated to contain 65:3 (LC), 48:15 (MC) or 34:33 (HC) % of the metabolizable energy (ME) from protein and carbohydrate, respectively. The diets were fed ad libitum for 4 weeks from parturition. Twelve dams were held in an intensive care unit and subjected to balance and respiration experiments and the kits were injected with deuterium oxide to measure water kinetics and milk production. Eighteen dams were kept under normal farm conditions and feed intake of dams and weight gain of the kits were determined. Milk samples were collected from the dams. Metabolizable energy intake was not affected by dietary treatment. Carbohydrates were efficiently utilized with a digestibility coefficient of 84% in dams fed the HC diet. Dams fed the HC diet had a lower (PO.05) percentage weight loss, lower (PO.05) total heat production (HE), lower (P<0.05) protein oxidation (OXP), lower (P<0.05) water intake and a lower (P<0.05) nitrogen (N) excretion than dams fed the LC diet. Milk production, and thereby liveweights of the kits 4 weeks post partum, was higher (P<0.05) in dams fed the HC diet than in dams fed the LC diet. In conclusion, lactating mink dams are able to utilize digestible carbohydrates with positive effects on lactation performance and reduced nitrogen excretion.
-Metabolic blood profiles were studied in a total of 30 female mink (Mustela vison) at different planes of nutrition prior to the breeding season in a control (CON; n = 10), a flushed (FLUSH; n = 10) and a negative energy balance group (NEG; n = 10). The
A total of 36 mink dams and their litters of 3, 6 or 9 kits were used for determination of milk intake of the suckling young by means of deuterium dilution technique, and chemical composition of milk and of kit bodies. Measurements were performed during lactation weeks 1-4, each week with 3 dams with each litter size. Milk intake was determined over a 48 h measurement period, and by the end of this milk samples were collected and 2 kits (litters of 6 and 9) or 1 kit per litter (litters of 3) were killed for body chemical composition. Based on the results, different models were applied for calculation of the energetic efficiency of milk. Dam milk yield increased steadily from week 1 until week 3 but only slightly from week 3 to 4. The increase declined with increasing litter size, and for dams suckling 9 kits the increment from week 3 to week 4 was only 2 g. The dry matter content of milk increased significantly as lactation progressed, being reflected in crude protein increasing from 6.9% in lactation week 1 to 8.1% in week 4. Milk fat increased concomitantly from 5.6% to 8.0%. In kit bodies, crude protein content increased from 9.4% in week 1 to about 12% in weeks 3 and 4. Body fat content increased from week 1 (4.1%) to week 3 (8.4%) and then declined in week 4 (7.1%). Animals suckled in litters of 3 kits had the highest milk intake and live weight and kits suckled in litters of 9 had the lowest milk intake, live weight and daily gain. In terms of milk intake per g gain kits in litters of 6 were the most efficient, with 4.1 g milk per g body gain. The metabolizable energy requirement for maintenance (MEm) was estimated to 448 kJ/kg(0.75 and the efficiency of utilization of ME for body gain (kg) to 0.67, the estimates being higher (MEm) or in good agreement with previous findings (kg) in suckling mink kits.
Thirty mink dams nursing litters of six kits were assigned to one of three dietary treatments [high protein (HP), medium protein (MP) and low protein (LP)], fed ad libitum for 4 week from parturition, to investigate the effects of protein supply on milk yield and milk composition in order to estimate the amino acid requirement of the lactating mink. Twelve dams were held in an intensive care unit and subjected to balance experiments and the kits were injected with deuterium oxide to determine water kinetics and milk yield. Eighteen dams were kept under normal farm conditions but with feed intake of dams and live weight gain of kits being determined and milk samples collected. The ME intake was higher (p < 0.05) in dams fed the LP and MP diets than in dams fed the HP diet, whereas the amino acid intake (g/day) was lowest (p < 0.05) in dams fed the LP diet. In the third and fourth weeks of lactation milk yield was higher (p < 0.05) in dams fed the LP and MP diets than in dams fed the HP diet. Chemical composition of milk was not affected (p > 0.05) by dietary treatment. However, protein content tended (p = 0.06) to be lower in dams fed the LP diet. Amino acid content (g/16 g N) of milk was higher (p < 0.05) in dams fed the LP and MP diets than in dams fed the HP diet. This resulted in the highest (p < 0.05) amino acid intake and highest (p < 0.001) live weights of kits nursed by dams fed the LP and MP diets, which may be explained by a combined effect of higher ME intake and reduced energetic costs for glucose production through less amino acids being used in gluconeogenesis. In conclusion, the improved performance of dams fed the LP diet suggested that their requirement of essential amino acids and non-specific N were covered, and the requirement of digestible amino acids of lactating mink (kg(0.75)) was, thereby, estimated by use of a factorial approach including the amino acid excretion in milk of LP dams.
-The mink is a seasonal breeder with induced ovulation and delayed implantation. Reproductive processes are strongly influenced by energy supply and body condition. Items for which there is paucity or complete lack of data were the main objectives of this study: the temporal relationship between copulation and the pre-ovulatory LH surge and the influence of energy supply on LH release. A total of 30 yearling female mink with a well defined metabolic status was used. Twelve females kept in the laboratory were measured in six consecutive one-week balance periods each including the measurement of heat production by means of indirect calorimetry, and 18 females were kept under conventional farm conditions. The animals were fed so as to maintain energy balance (CON), flush fed by 2 weeks food restriction followed by 2 weeks refeeding (FLUSH), or kept in a negative energy balance (NEG). Plasma concentrations of the thyroid hormones, IGF-1 and insulin were determined weekly (n = 12), or 1 week after change in energy supply to the FLUSH group (n = 18). On the day of mating, blood samples for LH and oestradiol-17β (E 2 ) were taken before and immediately after mating and then 4, 8, 12, 24, 30 and 48 h thereafter. Frequent blood samplings, each lasting 60 min, were taken during the LH surge from two other females surgically fitted with venous access ports. Peak concentrations of LH were recorded on the first sampling, an average 16 min after mating. The concentrations remained elevated for 12 h, but almost decreased to basal values 24 h after mating. Plasma E 2 was high before mating and peak values were attained 4 h after mating after which it decreased. Energy supply had no significant influence on LH and E 2 , but there was a tendency for a more sluggish LH release in NEG animals. The lack of response in FLUSH animals was explained by these animals having a lower intake of metabolisable energy than CON animals, the total intake not being significantly different from the NEG group. Plasma concentrations of thyroid Reprod. Nutr. Dev. 40 (2000) 229-247 229
Quantitative glucose metabolism in lactating mink (Mustela Øison) -Effects of dietary levels of protein, fat and carbohydrates .Glucose metabolism was measured during two consecutive years, 4 weeks postpartum, in a total of 36 yearling female mink, tted with jugular vein catheters and raising litters of six to seven kits. The dams were fed ad libitum from parturition on diets with different ratios of metabolizable energy (ME) derived from protein:fat:carbohydrate s (experiment 1: 61:37:2, 46:37:17, 31:37:32; experiment 2: 61:38:1, 47:52:1, 33:66:1). After 3 h fasting the dams were fed 210 kJ ME of the experimental diets. Two hours postprandially a single dose of 50 mCi U-1 4 C-and 2-3 H-labelled glucose was administered to each dam and blood samples were drawn 5, 10, 20, 30, 45 and 60 min after the tracer administration. Glucose turnover rates were 4 -5% min ¼ 1 in all dams, and the approximate daily glucose ux was 12 -17 g day ¼ 1 ; however, these were not signi cantly affected by dietary treatment. In conclusion, the mink is able both to synthesize large amounts of glucose de no×o and to utilize high levels of dietary digestible carbohydrates, and thereby to tolerate large variations in dietary carbohydrate supply.
Link to this article: http://journals.cambridge.org/abstract_S1357729800009061How to cite this article: R. Fink and A.-H. Tauson (1998). Flushing of mink ( Mustela vison): effects on energy metabolism and some blood metabolites. AbstractEnergy metabolism during flushing of mink (Mustela vison) in relation to a control group was studied by means of combining pooled data from balance and respiration experiments carried out in 1993 (experiment I) and 1994 (experiment II) and some blood metabolites from experiment II. The experiments, which were divided into six 1-week balance periods, started on 7 February and continued until 22 March. Flushing was performed by restricted feeding in periods 2 and 3 and refeeding in periods 4 and 5. Each balance period included a 24-h measurement of heat production by means of indirect calorimetry in open-air circuit respiration chambers. In experiment II blood samples were taken at weekly intervals and analysed for total triiodothyronine, total thyroxine, free thyroxine, glucose, insulin and fructosamine. Generally, intake of digestible nutrients and energy metabolism measurements within the flushed group were strongly influenced by period (energy supply), whereas they remained stable in the control group and differences between treatment groups over the total experiment were non-significant. The fluctuation in energy status induced by flushing did not involve major changes in body weight. Blood metabolites reflected the food intake by being fairly stable in the control group and decreasing during restriction and increasing during refeeding in the flushed group (P < 0-05). As an effect of flushing the number of corpora lutea increased significantly (P < 0-05).
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