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Title: Lipolysis in diabetic and non-diabetic participants, effects of nutrition and insulin treatment
Author: Alsini, Najlaa
Awarding Body: University of Surrey
Current Institution: University of Surrey
Date of Award: 2013
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Abstract:
Obesity, metabolic syndrome and type 2 diabetes are all characterised by insulin resistance and in most cases large intra-abdominal fat stores. Insulin resistance is associated with the dysregulation of adipose tissue (AT) Metab including a reduced effectiveness for insulin to suppress lipolysis. Although patients with type 2 diabetes arc treated with metformin initially. the majority of patients eventually need treatment with insulin to maintain glucose control. Insulin treatment with most types of insulin therapy is associated with weight gain. However the insulin analogue detemir is weight neutral or causes weight loss and it has been suggested that this may be related to a reduced effect of this' insulin in peripheral tissues such as AT. A high sugar intake (fructose and sucrose) is associated with insulin resistance but the effects' on AT Metab are not established. Methods were developed to measure cell sizes, in vitro basal, stimulated and insulin inhibited lipolysis and lipoprotein lipase (LPL) activity in AT biopsies, These methods were then applied to study a) subcutaneous AT (SCAT) and omental AT (OMAT) biopsies from twelve participants, seven non-diabetic subjects and five patients with type 2 diabetes treated with metformin (T20H) undergoing abdominal surgery and b) the effect of treatment of patients with type 2 diabetes with insulin detemir (n=7) or insulin neutral protamine hagedorn (NPH) (n~5), in a 16 week parallel group study. The effect of sugar intake on the in vivo rate of lipolysis and post-heparin lipolysis was investigated in 25 men at risk of metabolic syndrome, In a cross-over study design participants were studied after a 12 week diet high in extrinsic sugars and low in extrinsic sugars Adipocyte size of SCAT and OMAT was significantly larger in T20H than healthy participants (p<0.001, p<0.05 respectively). In healthy subjects OMAT had higher basal, isoproterenol stimulated and insulin inhibited lipolysis than SCAT (p<0.0I, p<0.001, p<0.05 respectively). In participants with T20R, stimulated lipolysis with isoproterenol in SCAT was significantly higher than OMAT. but there was no significant difference in basal and insulin inhibited lipolysis. There was no significant difference between healthy and T20H in SCAT lipolytic activity, but OMAT has higher basal, isoproterenol stimulated and insulin inhibited lipolysis than SCAT (p<0.05, p<0.001, p<0.01 respectively) in healthy participants. LPL activity in OMAT was significantly higher than SCAT in both healthy and T20H group (p<0.001,p<0.05 respectively). In the insulin detemir clinical trial, fasting non-esterified fatty acids (NEFA) decreased significantly with detemir compared to NPH (p<0.05) . Basal lipolysis in the fat biopsies showed a significant reduction with detemir treatment (p<0.05) with no significant change following NPH treatment. LPL mass and activity increased significantly after 16 weeks treatment with detemir compared to NPH (p=0.006, p=0.005). No significant differences were observed on stimulated lipolysis or adipocyte size following either of the treatments. In the dietary intervention study after the high sugar diet compared with low 'sugar diet, liver fat, fasting plasma glucose and NEF A concentrations were significantly higher in men with higher liver fat at screening (all p<0.05). In the low-liver fat group, plasma TG (p=0.07) NEF A (p=0.04) and LPL activity (p<0.05) were higher after the low versus high sugar diet, whereas, in the high-liver fat group, hepatic lipase (HL) activity was higher after the high versus the low sugar diet (p<0.05). The palmitate (P A) concentration decreased significantly after the high sugar diet compared with low sugar diet (p<0.001) in the high liver fat group. In this group, the percentage of palmitate to total NEFA in the circulation (P A:NEF A) decreased significantly after the high sugar diet, this value was significantly lower than the value after the high sugar diet in the low liver fat group (p<0.05). However, the palmitate rate of appearance increased after the high sugar diet in the high liver fat group, but did not reach significance (p=0.06). Conclusion: This study showed that OMAT had less sensitivity to insulin action than SCAT in T20H. In the clinical trial of insulin detemir, the decrease in basal NEFA levels and basal lipolysis and the increased LPL mass and activity suggests that detemir improves fasting insulin sensitivity. This may be due to a greater hepatoselective action of detemir reducing over-insulinisation of adipose tissue and skeletal muscle. The change in plasma lipid Metab and pattern of response in lipase activities in response to a diet high in extrinsic sugars increased the availability of NEFA from peripheral and endothelial lipolysis; this may be due to reduced insulin sensitivity in participants with high liver fat.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.606797  DOI: Not available
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