- Open Access
Improved glucose tolerance in acyl CoA:diacylglycerol acyltransferase 1-null mice is dependent on diet
© Wang et al; licensee BioMed Central Ltd. 2007
- Received: 10 November 2006
- Accepted: 19 January 2007
- Published: 19 January 2007
Mice that lack acyl CoA:diacylglycerol acyltransferase (Dgat1-/- mice) are reported to have a reduced body fat content and improved glucose tolerance and insulin sensitivity. Studies so far have focussed on male null mice fed a high fat diet and there are few data on heterozygotes. We compared male and female Dgat1-/-, Dgat1+/- and Dgat1+/+ C57Bl/6 mice fed on either standard chow or a high fat diet.
Body fat content was lower in the Dgat1-/- than the Dgat1+/+ mice in both experiments; lean body mass was higher in male Dgat1-/- than Dgat1+/+ mice fed on the high fat diet. Energy intake and expenditure were higher in male Dgat1-/- than Dgat1+/+ mice; these differences were less marked or absent in females. The body fat content of female Dgat1+/- mice was intermediate between that of Dgat1-/- and Dgat1+/+ mice, whereas male Dgat1+/- mice were similar to or fatter than Dgat1+/+ mice. Glucose tolerance was improved and plasma insulin reduced in Dgat1-/- mice fed on the high fat diet, but not on the chow diet. Both male and female Dgat1+/- mice had similar glucose tolerance to Dgat1+/+ mice.
These results suggest that although ablation of DGAT1 improves glucose tolerance by preventing obesity in mice fed on a high fat diet, it does not improve glucose tolerance in mice fed on a low fat diet.
- Lean Body Mass
- Brown Adipose Tissue
- Chow Diet
- Improve Glucose Tolerance
- Wildtype Mouse
The final step of triglyceride synthesis in mammals is catalysed by the enzymes acyl CoA:diacylglycerol acyltransferase 1 and 2 (DGAT1 and DGAT2), which have dissimilar amino acid sequences. Both enzymes are widely expressed and are highly expressed in adipose tissue and liver . Previous reports have described resistance to diet-induced obesity  and amelioration of obesity due to the A y , but not the Lep ob or LepR db , mutation  in DGAT1-deficient (Dgat1-/-) mice. Resistance to obesity was associated with increased reductions in body weight and food intake in response to peripherally but not centrally administered leptin [3, 4]. Food intake relative to body weight was either unchanged  or raised [3, 4], and energy expenditure relative to body weight was raised , suggesting that the primary effect of DGAT1 deficiency is on the energy expenditure side of the energy balance equation. Increased locomotor activity and brown adipose tissue thermogenesis have been invoked to account for increased energy expenditure [2, 3, 5]. It appears, however, that fat oxidation is increased in liver as well as skeletal muscle and brown adipose tissue because the concentration of diacylglycerol was reduced in the liver of Dgat1-/- mice . This finding is paradoxical since one might expect the concentration of diacylglycerol – the substrate of DGAT1 – to be raised in Dgat1-/- mice, but it can be rationalised if fat oxidation is somehow increased.
Stimulation of fatty acid oxidation is usually associated with improved insulin sensitivity and glucose tolerance, possibly because the concentrations of lipid metabolites that inhibit the insulin signalling pathway (e.g. long chain fatty acyl CoA, diacylglycerol, ceramide) are reduced . Moreover, in the longer term, insulin sensitivity will improve due to the reduced plasma non-esterified fatty acid concentration and altered adipokine profile associated with decreased adipocyte lipid stores. Therefore it is not surprising that Dgat1-/- C57Bl/6 mice have been reported to show improved insulin sensitivity [3, 7, 8]. However, overexpression of DGAT1 in adipose tissue of C57Bl/6 mice was associated with obesity but not with impaired glucose disposal . By contrast, overexpression of DGAT1 in adipose tissue of FVB mice, a strain known to be resistant to diet-induced obesity, was not associated with obesity, but was associated with insulin resistance . These results support the view that an increased capacity for triacylglycerol synthesis is not detrimental to insulin sensitivity provided it is confined to adipocytes and newly formed adipocytes can accommodate any excess triacylglycerol.
We found in a pilot experiment  that, in contrast to a previous report  glucose tolerance and insulin tolerance were actually worse, and fasting plasma insulin was raised in Dgat1-/- compared to wildtype mice fed on a chow (low fat) diet. The knockout mice appeared to border on a state of 'functional lipodystrophy'. The wildtype mice used in this pilot experiment were age-matched to the Dgat1-/- mice rather than being littermates, raising the possibility that a minor variation in genetic background could have been responsible for the difference. We have therefore now compared Dgat1-/- and littermate Dgat1+/+ mice fed on both chow and high fat diets with respect to glucose homeostasis and energy balance. While we do not repeat the finding of impaired glucose tolerance, we do find that it is only on the high fat diet that glucose tolerance is improved in the Dgat1-/- mice. Since there are limited data on the phenotype of heterozygote (Dgat1+/-) mice , these were included in the study to give some perspective on how much inhibition of DGAT1 might be required to treat obesity and type 2 diabetes. We also compared the effects of knockout of the Dgat1 gene in both male and female mice, whereas previous studies have focussed on males.
Terminal plasma leptin and perigenital fat pad weights
2.2 ± 1.8
4.4 ± 1.8***
1.5 ± 0.4
5.5 ± 3.7
4.2 ± 2.4
1.9 ± 0.2
Fat pad weight (g)
0.50 ± 0.07
0.78 ± 0.11*
0.32 ± 0.03***
0.70 ± 0.08
0.56 ± 0.08
0.31 ± 0.05***
High fat diet:
16.3 ± 2.1
16.0 ± 2.4
1.2 ± 0.3***
21.1 ± 1.5
19.6 ± 2.2
2.8 ± 0.3***
Fat pad weight (g)
1.57 ± 0.13
1.52 ± 0.7
0.32 ± 0.04***
1.67 ± 0.18
1.31 ± 0.15
0.48 ± 0.14***
Our results are consistent with a previous report  in showing that Dgat1-/- mice have a lower body fat content than Dgat1+/+ mice and are resistant to diet-induced obesity. They also agree that energy turnover is increased in male Dgat1-/- mice, although this was less evident in female Dgat1-/- mice. They differ, however, from previous reports that show  or imply  that glucose tolerance is improved in Dgat1-/- mice fed on a chow diet.
Body fat content was higher in the Dgat1+/+ mice fed on the high fat diet compared with the same mice fed on the chow diet, but it was similar in Dgat1-/- mice fed on the high fat and chow diets. Consequently, the effect of ablation of the gene was greater in mice fed on the high fat diet. The effect of ablation of the Dgat1 gene was as apparent in female as in male mice, which have been the focus of previous studies.
Why the absence of an enzyme involved in triacylglycerol synthesis should increase fat oxidation and energy expenditure is not known. One study suggested that a factor released in increased amounts from the adipose tissue of Dgat1-/- mice could play a role , but it seems unlikely that this factor is adiponectin [1, 12]. Plasma adiponectin was decreased in male Dgat1-/- mice in our pilot experiment , which is also inconsistent with this hypothesis. Increased locomotor activity in Dgat1-/- mice raises the possibility that ablation of DGAT1 in the brain raises energy expenditure in the periphery. Thus hypothalamic lipid metabolites are known to affect energy expenditure . However, overexpression of DGAT1 in adipose tissue alters body composition [9, 10], and overexpression of DGAT1 in rat isolated islets of Langerhans increases triglyceride synthesis . Therefore, at least in adipose tissue and islets, DGAT1 can have a direct effect on triglyceride storage.
An unexpected finding that may in part account for increased energy expenditure in male Dgat1-/- mice was that lean body mass, which has more influence on energy expenditure than fat mass [15–17], was increased in male Dgat1-/- mice fed on the high fat diet. Lean body mass was not raised significantly in the particular group – male Dgat1-/- mice – where energy expenditure was significantly raised in the present study, but energy expenditure was measured at 12 weeks of age and body composition at 20 weeks of age. Other workers have not observed increased lean body mass in Dgat1-/- mice , although a trend to increased percentage protein content in Dgat1-/- mice fed on a chow diet has been reported .
Our finding that glucose tolerance was not improved in Dgat1-/- mice fed on a chow diet compares with studies on the overexpression of DGAT1. This did not result in impaired glucose disposal in a strain of mice that was able to respond with increased adipose tissue fat stores , but did cause insulin resistance in a strain that was unable to accommodate extra lipid in adipocytes . In the current study, in contrast to our pilot experiment , ablation of DGAT1 did not impair glucose tolerance, but nevertheless, inhibition of lipid synthesis in animals that have a low capacity for adipocyte triglyceride accumulation may risk exacerbating insulin sensitivity. In this regard, it is interesting that lipodystrophic animals and humans are characterised by insulin resistance  and a recent report suggests that lipodystrophic humans have an increased lean body mass , a feature displayed by male Dgat1-/- mice in the current work.
There were no significant differences between the heterozygote (Dgat1+/-) and Dgat1+/+ mice, except for the surprising finding of increased fat pad weights and leptin concentration in the male Dgat1+/- mice fed on chow. This contrasts with a previous report that male heterozygote mice had a total fat pad weight intermediate between Dgat1-/- and Dgat1+/+ mice . Female heterozygote mice, by contrast, did have an intermediate phenotype in terms of fat mass (Fig. 2). Perhaps compensatory mechanisms, such as increased DGAT2 activity, were more pronounced in males than in females. Glucose tolerance was very similar in heterozygote and wildtype mice. This suggests that to treat type 2 diabetes with an inhibitor of DGAT1 it may be necessary to inhibit activity markedly. The activities of DGAT1 in the wildtype and heterozygote mice were not compared, however.
Dgat1-/- mice had a lower body fat content than wildtype mice and males had an increased lean body mass when they were fed on a high fat diet. Improved glucose tolerance and reduced plasma insulin levels were apparent only when the mice were fed on a high fat diet. Inhibition of triglyceride synthesis does not improve glucose tolerance if adipocyte lipid stores are already low.
Procedures were conducted in accordance with the University of Buckingham Home Office UK project licence under the Animals (Scientific Procedures) Act (1986) and as agreed by the University of Buckingham Ethical Review Board.
Three male Dgat1-/- and three female Dgat1+/- mice back-crossed onto a C57Bl/6 background for ten generations (B6.129S4 – Dgat1tm 1Far/J) were purchased from Jackson Laboratories (Bar Harbor, Maine, USA) and a colony was expanded in our facilities, breeding from male Dgat1-/- and female Dgat1+/- mice. The method used to delete the Dgat1 gene has been reported previously . The offspring from the breeding of the Dgat1-/- and Dgat1+/- mice were genotyped between 4 to 5 weeks of age and in order to generate littermates of all three possible genotypes, male and female Dgat1+/- mice were used for further rounds of breeding to obtain the experimental mice. Genomic DNA was extracted from tail tip samples and Dgat1 and neomycin genes detected by PCR using the primers previously described . The presence of both neomycin and Dgat1 genes indicated heterozygosity.
The mice were fed on a standard chow diet that contained 10% fat, 70% carbohydrate and 20% protein by energy (14.0 kJ/g metabolisable energy; Beekay Feed, B&K Universal Ltd., Hull, UK), or they were fed on chow until they were 12 weeks old and then on a sweetened high fat diet that contained by energy 45% fat, 35% carbohydrate (of which half was sucrose) and 20% protein (19.3 kJ/g metabolisable energy; diet code D12451; Research Diets, New Brunswick, USA). They were housed at 22°C with lights on from 07.00 to 19.00 h.
There were twelve mice of each sex and genotype (Dgat1+/+, Dgat1+/- and Dgat1-/-) housed in threes, except that only six female Dgat1-/- mice were fed on the high fat diet. Food intake for each cage of mice was measured daily and body weight was measured weekly from the age of 9 or 13 weeks in the chow or high fat diet experiments, respectively. Energy expenditure was measured at 12 weeks of age in mice fed on the chow diet. Glucose tolerance tests were performed at 15 and 24 weeks of age in the chow and high fat diet experiments respectively. The mice were killed after a 5-hour fast aged 20 (chow diet) or 30 (high fat diet) weeks and blood was taken for the measurement of plasma leptin (Crystal Chem Inc, Chicago, IL). Body composition was determined by dual energy X-ray absorptiometry (Lunar PIXImus 2 mouse densitometer and version 1.46 software; GE Medical, Bedford, UK).
Mice were fasted for 5 h from 09.00 h before administration of glucose (2 g/kg, i.p. body weight). Blood samples were taken from the tip of the tail after the topical application of a local anaesthetic (lignocaine gel) at 30-minute intervals. Glucose and insulin were measured as described previously .
Energy expenditure was measured over 24 h, beginning at 10.00 h in the mice's home cage by open circuit indirect calorimetry using the equation of Weir . The volume of the mouse cages was 23 litres and the flow rate was 0.8 l/min. Such a system has a calculated half-life of 23.5 min for responding to a step change in energy expenditure . It is therefore not suitable for instant measurement of energy expenditure but with the mice undisturbed in their home cages, it is ideal for measurement of daily energy expenditure. The energy expenditure of all the male mice of all the different genotypes was measured in a single run over 24 h and after recalibration, the energy expenditure of all the female mice was measured on the following day.
Results are presented as means ± S.E. They were analysed by one-way analysis of variance followed by Bonferroni's post-test for selected comparisons (wild-type mice with heterozygous or homozygous mutant mice of the same sex) unless stated otherwise.
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