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GKEN
22 (1998) 141-144
TBTAK
Received : 17.07.1996
Abstract: In order to provide uniqe insight into the metabolic disturbences seen after calving cholesterol, triglycerid, high density
lipoprotein, low density lipoprotein, very low density lipoprotein, glucose and insulin levels in serum were studied before calving
(group I), in aerly (group II) and late (group III) lactation in 24 normal cows.
Serum lipoproteins were separeted into various density classes by repeated ultracentrifugation.
The results indicate that there was a rise in glucose, tryglycerid and very low density lipoprotein levels before calving, and in choles-
terol and high density lipoprotein levels late lactation, and the dairy cows were inclined fatty liver because of lower very low density
lipoprotein and glucose levels in early and late lactation, and were inclined hyperketonemia in early lactation because of lower insulin
level than in late lactation.
Key Words:Lipid, lipoproteins glucose, insulin, pre and postpartum, cows
141
Peri and Postparturient Concentrations of Lipid Lipoprotein Insulin and Glucose in Normal Dairy Cows
probably by this way the cholesterol an the VLDL- until analysis by radioimmunassay (Insulin RIA 100,
fraction is formed. It is not known if a de novo synt- Pharmacia Diagnostics AB, uppsala, Sweden).
nesis of HDL occurs in the liver in cattle. Glucose, cholesterol and triglycerids were deter-
There are large variations in fat metabolism during mined by commercial enzymatic kits (Boenringer
different stages of lactation and pregnancy and the Mannhein Diagnostica).
risk of disturbances are also variable. The Fishers F test and Duncans multiple Range
The distrubution of glucos to different tissues, and test were used to analyse data (9).
thereby also gluconeogenesis is regulated by the two
pancreatic hormones, insulin and glucagon. They have
opposing and counterbalancing actions: glucagon stimu- Results
lates and insulin inhibits gluconeogenesis (4). Insulin The glucose, triglycerid and VLDL levels were sig-
and glucagon also regulate lipolysis in fat tissues and nificantly higher in periparturient cows than in early
ketogenesis in the liver (5). Insulin and glucagon are and late lactation. The cholesterol and HDL levels were
thus very important regulatory factors in the adapta- also significantly higher in cows in late lactation than
tion of the energy metabolism. The requirment of of the other two groups. The insulin and LDL concen-
energy at calving that is not supplied by feed comp- trations in periparturient cows were significantly lower
sumption is met by increased lipolysis and by glycone- than in late lactation (Figure 1,2,3).
ogenesis from glycogen and from tissue protein. To
achieve this, there is continuous depression of the
basal plasma insulin levels before calving (6). Lomax et Discussion
al. (7) have shown that insulin production was more
Plasma lipoproteins are complex molecules that are
than twice as high in nonlactating cows.
heterogeneous in composition, size and biological activ-
The objective of the present study was to analyse ity. According to Raysiguier et al. (10) the most sig-
basal blood levels of lipid, lipoproteins, insulin and glu- nificant result obtained two weeks postpartum in cows
cose in cows around calving and in lactation and to with sever fatty liver was the dramatically decrease in
provide unique insight into the metabolic disturbances plasma HDL and VLDL. During these same period the
seen after calving. animals in the moderately steatosic group were no dif-
ferent from the controls as regards the LDL. In con-
trast, by the fourth week, the moderately steatosic
Material and Methods animals had an LDL fraction that was significantly
Twenty four healthy and mature Swiss Brown lower than control animals. In normal cows, lipid infi-
Cows in late pregnancy (group I, n=8), ealy (group II, tration of the liver postpartum, diferent workers have
n=8) and late (group III, n=8) lactation from Konya shown that lipid infiltration reached a maximum one
Central animal Research Instituts dairy herd were to two week postpartum, and regresed rapidly.In the
used. Group I of cows were in dry period, group II of present study, VLDL levels of cows in postpartum
cows in the first month and group III of cows in the early and late lactation were also significantly lower
fourth month after calving. The milk yieds in previous than in periparturient, and HDL level of cows in late
lactations had been at least 4000 kg. lactation was significantly higher than in periparturi-
ent and in early lactation. The results from the stud-
Blood samples were taken from the jugular vein ied indicates that the dairy cows are inclined fatty
before the morning feeding and at 3 h after this. liver after calving. Because, Holtenius and Hjort (1)
VLDLs were isolated at plasma density d<1.006 g/ show that accumulation of fat in the liver cells and
ml by centrifugation at 100.000 g for 18 hours. development of fatty liver is caused by reduced syn-
Other lipoprotein fractions were isolated by sequen- thesis of VLDL. The reduced syntesis is most probably
tially raising the plasma density to d=1.063 g/ml LDL, associated with feeding factors. High energy-low pro-
and 1.21 g/ml HDL by adding crystalline potassium tein prepartum feeding is shown to be such a factor.
bromide and centrifugation at 100.000 g for 20 and There was significant alteration in LDL levels between
40 hours, respectively (8). periparturient cows and in late lactation.
Serum for insulin determinations was obtained In the normal cows there is a rise in FFA-level and
after centrifugation within 2 hours and kept at -20 C a reduction in cholesterol and phospholipids from 6
142
A. BAOLU, M. SEVN, M. OK, M. GKEN
0
-
-
A B C
100
mg/dl
Cholesterol
Triglycerid
50
19,9
6,94 8,41
0
A B C
A: before calving B: early lactation C: late lactation
75
HDL
mg/dl
LDL
50 VLDL
35,8
30,9
23,9
25
week before to the day after calving. During the fol- and in early lactating cows, and there was a rise tri-
lowing 6 weeks the level increased continously. How- glycerid level in periparturient cows.
ever, the cows with fatty livers had lower amounts of A degree of hipoglycemia was apparent in peripar-
cholesterol. In the present study, cholesterol level in turient cows which was more marked before than
late lactating cows was olso higher than before calving after calving (11). In contrast, in the present study,
143
Peri and Postparturient Concentrations of Lipid Lipoprotein Insulin and Glucose in Normal Dairy Cows
serum glucose concentration was significantly higher in exceeds the feed consumption capacity. However, this
periparturient cows than in ealy and late lactation. energy deficit in ealy lactation is compansated by
According to Holtenius et al.(12), before calving mobilisation of stored energy. By the mobilisation of
the feeding regimen had a very strong ihfluence on fat, some degree of hyperketonemia without clinical
the basal insulin level. High amount of concentrate signs can occur and is considered as physiological.
increased basal insulin levels until one week before Baird (14) has reported that clinical ketosis occurs at
calving and caused an interruption in the physiological a minimum blood acetoacetate concentration of about
decreasing course. After calving the insulin levels were 0.5 mmol/L. Fat mobilisation is stimulated by low
low in all groups of cows. Hyperketonemic cows had insulin activity.
lower insulin than normal cows. However, there was In conclusion, the dairy cows in the study were
continuous depression of the basal plasma insulin level inclined fatty liver after calving because of lower VLDL
before calving (6). In the present study, the insulin and glucose levels in early and late lactations and were
level was also higher significantly in late lactating cows inclined hyperketonemia in early lactation because of
than in periparturient accordance with this and Stau- lower insulin level than in late lactation. The deter-
fenbiel et al.(13). mined parameters, thus can provide unique insght into
Almost all newly calved high producing dairy cows the metabolic disturbances seen after calving.
are in negative energy balance as energy requirement
144