Effects of insulin-induced hypoglycaemia on lipolysis rate, lipid oxidation and adipose tissue signalling in human volunteers: a randomised clinical study
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The aims of this study were to determine the role of lipolysis in hypoglycaemia and define the underlying intracellular mechanisms.
Nine healthy volunteers were randomised to treatment order of three different treatments (crossover design). Treatments were: (1) saline control; (2) hyperinsulinaemic hypoglycaemia (HH; i.v. bolus of 0.1 U/kg insulin); and (3) hyperinsulinaemic euglycaemia (HE; i.v. bolus of 0.1 U/kg insulin and 20% glucose). Inclusion criteria were that volunteers were healthy, aged >18 years, had a BMI between 19 and 26 kg/m2, and provided both written and oral informed consent. Exclusion criteria were the presence of a known chronic disease (including diabetes mellitus, epilepsy, ischaemic heart disease and cardiac arrhythmias) and regular use of prescription medication. The data was collected at the medical research facilities at Aarhus University Hospital, Denmark. The primary outcome was palmitic acid flux. Participants were blinded to intervention order, but caregivers were not.
Adrenaline (epinephrine) and glucagon concentrations were higher during HH than during both HE and control treatments. NEFA levels and lipid oxidation rates (determined by indirect calorimetry) returned to control levels after 105 min. Palmitate flux was increased to control levels during HH (p = NS) and was more than twofold higher than during HE (overall mean difference between HH vs HE, 114 [95% CI 64, 165 μmol/min]; p < 0.001). In subcutaneous adipose tissue biopsies, we found elevated levels of hormone-sensitive lipase (HSL) and perilipin-1 phosphorylation 30 min after insulin injection during HH compared with both control and HE. There were no changes in the levels of adipose triglyceride lipase (ATGL), comparative gene identification-58 (CGI-58) or G0/G1 switch gene 2 (G0S2) proteins. Insulin-stimulated phosphorylation of Akt and mTOR were unaffected by hypoglycaemia. Expression of the G0S2 gene increased during HE and HH compared with control, without changes in ATGL (also known as PNPLA2) or CGI-58 (also known as ABHD5) mRNA levels.
These findings suggest that NEFAs become a major fuel source during insulin-induced hypoglycaemia and that lipolysis may be an important component of the counter-regulatory response. These effects appear to be mediated by rapid stimulation of protein kinase A (PKA) and HSL, compatible with activation of the β-adrenergic catecholamine signalling pathway.
The study was funded by Aarhus University, the Novo Nordisk Foundation and the KETO Study Group/Danish Agency for Science Technology and Innovation (grant no. 0603–00479, to NM).
KeywordsAdrenaline ATGL HSL Hypoglycaemia Insulin Intracellular signalling Lipid oxidation Lipolysis PKA
AMP-activated protein kinase
Adipose triglyceride lipase
Comparative gene identification-58
G0/G1 switch gene 2
Mammalian target of rapamycin
Protein kinase A
Lipid droplet-associated protein
Hypoglycaemia is counteracted by a cascade of behavioural, hormonal and metabolic events. In healthy volunteers, this defence mechanism involves a reduction in endogenous insulin secretion, release of the counter-regulatory hormones glucagon, adrenaline (epinephrine), growth hormone (GH) and cortisol, and carbohydrate ingestion [3, 4, 5]. Individuals with type 1 diabetes mellitus depend entirely on exogenous insulin and cannot reduce endogenous insulin production during hypoglycaemia. Furthermore, with long-standing disease and recurrent episodes of hypoglycaemia, the counter-regulatory hormonal responses to hypoglycaemia become compromised (due to loss of glucagon response and hypoglycaemia-associated autonomic failure) [2, 6], rendering these individuals particularly vulnerable to hypoglycaemia.
Hormonal responses to hypoglycaemia have profound metabolic effects in healthy individuals, leading to increased endogenous glucose production and decreased glucose disposal. In addition, lipolysis is acutely stimulated by adrenaline  and, after a delay, by GH  and cortisol . A series of studies in healthy volunteers during insulin-induced hypoglycaemia, have shown that NEFA and 3-hydroxybutyrate (3-OHB) levels and lipid oxidation rates are restored after some hours to above basal levels [10, 11]. Furthermore, these studies demonstrate that increased lipolysis plays a pivotal role in mediating hypoglycaemia-associated insulin resistance [10, 11]. Very few studies have measured the actual rates of lipolysis during hypoglycaemia. In apparent contrast with these findings, one study reported unchanged rates of lipolysis in healthy volunteers, measured using [14C]palmitate after insulin-induced hypoglycaemia with mean glucose nadir of ≈2.8 mmol/l . Another study from the 1960s reported increased NEFA production in sheep following hypoglycaemia, as measured with [9,10-3H2]palmitate .
Similarly, the intracellular signalling mechanisms in adipose tissue (AT) that regulate lipolysis in response to hypoglycaemia in humans are unclear. Lipolysis is regulated by adipose triglyceride lipase (ATGL), hormone-sensitive lipase (HSL) and monoacylglycerol lipase (MAGL), which hydrolyse triacylglycerol to form NEFAs and glycerol .This process is mediated by protein kinase A (PKA), which phosphorylates HSL and lipid droplet-associated protein (PLIN1). Phosphorylation of PLIN1 leads to the dissociation of comparative gene identification-58 (CGI-58) from PLIN1, and it then binds to and strongly increases the activity of ATGL . The counter-regulatory G0/G1 switch gene 2 (G0S2) protein is a major inhibitor of ATGL . PKA is activated by catecholamines, which act via β-adrenergic receptors to activate adenylyl cyclase and increase intracellular cAMP . The intracellular signalling events in AT that lead to increased lipolysis during hypoglycaemia are largely unknown.
Consequently, our study was designed to test whether hypoglycaemia induces a detectable increase in the rate of lipolysis, as measured with labelled palmitate, and whether this is associated with activation of intracellular signalling in AT. Based on previous observations of a central role for adrenergic mechanisms, we hypothesised that PKA activity and subsequently HSL phosphorylation would increase.
A randomised, crossover study was conducted involving nine male volunteers over three study days. Randomisation was performed using Research Randomizer (www.randomizer.org). Inclusion criteria were that volunteers were healthy, aged >18 years, had a BMI between 19 kg/m2 and 26 kg/m2, and provided both written and oral informed consent. Exclusion criteria were the presence of a known chronic disease (including diabetes mellitus, epilepsy, ischaemic heart disease and cardiac arrhythmias) and regular use of prescription medication. Each volunteer was randomly allocated for the order of three treatments: (1) control (i.v. bolus of 2 ml NaCl); (2) hyperinsulinaemic hypoglycaemia (HH; i.v. bolus of insulin [0.1 U Actrapid/kg in 2 ml NaCl]; and (3) HE (i.v. bolus of insulin [0.1 U Actrapid/kg in 2 ml NaCl] and 20% glucose). During HE, glucose levels were clamped based on frequent (every 5 min) measurements of plasma glucose. Volunteers were blinded to treatment and reported to the clinical research unit at 07:50 hours on each study day, after a 10 h fast. One i.v. catheter was inserted into the right antecubital vein for infusions and another was inserted, in a retrograde fashion, into the left antecubital vein for measuring venous blood glucose from the forearm (arteriovenous blood glucose measurements were not used in this study). A third i.v. catheter was inserted into a dorsal hand vein on the volunteer’s right hand for sampling arterialised blood with the heated hand technique [16, 17, 18]. Each volunteer was placed in a supine position in a thermoneutral room and each study day commenced at 09:00 hours (t = 0 min) with the injection of one of the three interventions. Volunteers were assessed from 09:00 to 10:45 hours (t = 0–105 min).
Each of the study days were separated by a minimum of 21 days.
Abdominal subcutaneous fat biopsy
Abdominal subcutaneous fat was biopsied under sterile conditions 15 min after local anaesthesia (1% lidocaine, 10 ml) was applied. Biopsies were obtained from the right side at t = 30 min and from the left side at t = 75 min. See electronic supplementary material (ESM) Methods for further details.
Western blotting analyses were performed using 4–15% Criterion XT Bis-Tris gels (Bio-Rad, Hercules, CA, USA). Primary antibodies against HSL (no. 4107), p-HSL Ser563, Ser565 and Ser660 (nos 4139, 4137 and 4126; measuring p-HSL Ser552, Ser554 and Ser650 in human AT), mammalian target of rapamycin (mTOR; no. 2972), p-mTOR Ser2448 (no. 5536), PKA substrate (no. 9624), AMP-activated protein kinase α (AMPKα) (no. 2532), p-AMPK Thr172 (no. 2531; all from Cell Signaling, Danvers, MA, USA), ATGL (no. GTX62840; GeneTex, Irvine, CA, USA), CGI-58 (ab183739, Abcam, Cambridge, UK) and G0S2 (sc-133424, Santa Cruz Biotechnology, Santa Cruz, CA, USA) were obtained from the respective supplier. Protein phosphorylation is expressed as a ratio compared with total protein expression as measured on the same membrane. Protein levels are expressed as a ratio to total protein content in the sample as measured by stain-free protein technology . Stain-free protein technology was also used to demonstrate equal loading. See ESM Methods.
mRNA was isolated and quantified by quantitative PCR (qPCR) analysis using standard protocols. See ESM Methods.
Plasma glucose was measured using the glucose oxidase method (YSI 2300 STAT plus, YSI Life Sciences, Yellow Springs, OH, USA). Serum insulin was measured using ELISA (Dako, Glostrup, Denmark). C-peptide was measured by ELISA (Alpco, Salem, NH, USA). Serum NEFA was measured using a commercial kit (Wako Chemicals, Neuss, Germany). Plasma glucagon was measured using a RIA kit (EMD Millipore, Darmstadt, Germany). Plasma adrenaline and noradrenaline (norepinephrine) were measured by electrochemical detection following HPLC . 3-OHB was measured by hydrophilic interaction liquid chromatography-tandem MS .
Palmitic acid flux
Palmitic acid flux was measured with the isotope dilution technique by [9,10-3H]palmitic acid (0.3 μCi/min = 10.500 Bq/min) infusion from t = 30 min to t = 105 min. Blood samples used to measure palmitic acid concentration and specific activity (ratio between isotope and total palmitic acid levels) were obtained at baseline (t = 0 min) and at t = 60, 75, 90 and 105 min. Palmitic acid concentration and specific activity were measured using [2H31]palmitic acid as an internal standard . A quality control standard was included in every assay.
The primary outcomes were palmitic acid flux and changes in the phosphorylation levels of target proteins during HH.
Statistical analyses were performed using Stata version 13.0 (StataCorp, College Station, Texas, USA), with a repeated measurement mixed model that included visit number, visit order, time, intervention and the interaction between time and intervention as factors. A value of p < 0.05 was considered statistically significant. Graphs have crude geometric means with SEM. Numerical data are presented as adjusted geometric means and 95% CIs. Western blotting protein measurements are given as the ratio to the mean control value at t = 30 min. See ESM Methods.
Data on the effects of hypoglycaemia on ghrelin concentrations have been published previously .
The study protocol was approved by the local scientific ethics committee (1-10-72-113-13). The study was conducted in accordance to the Helsinki Declaration II and volunteers gave both oral and written informed consent.
Characteristics of participants
Baseline characteristics of the nine volunteers
3.7 (0, 7.4)
Systolic BP (mmHg)
124 (117, 131)
Diastolic BP (mmHg)
75 (71, 80)
4.6 (3.0, 6.1)
5.0 (4.6, 5.5)
30 (28, 32)
4.9 (4.7, 5.1)
TSH (10−3 IU/l)
C-reactive protein (mg/l)
Glucose infusion during HE
The glucose infusion rate required to maintain euglycaemia during HE quickly reached a peak level of 13.5 (95% CI 12.5, 14.6) mg/kg/min at t = 15 min, followed by a slow decrease toward zero at t = 105 min (data not shown).
Hormone and substrate levels
All baseline measurements of insulin, C-peptide, adrenaline, glucagon, GH, glucose, NEFA, 3-OHB, lactate and noradrenaline were comparable among interventions.
During HH, C-peptide concentrations were rapidly reduced (Fig. 1b). A mean nadir of 96 (95% CI 51, 142) pmol/l was observed at t = 60 min. During HE, C-peptide levels were initially reduced, but increased at t = 30 min to exceed control levels (p < 0.01). The peak C-peptide level during HE was 569 (95% CI 502, 636) pmol/l at t = 45 min. During control treatment, mean C-peptide concentrations remained unaltered, with an overall mean of 352 (95% CI 312, 391) pmol/l.
Adrenaline concentrations markedly increased during HH compared with HE and control treatment (Fig. 1c). During HH, a peak adrenaline value of 891 (95% CI 560, 1221) pg/ml was observed at t = 30 min; the concentration at the equivalent time point during HE was 43 (95% CI 8, 79) pg/ml (p < 0.001). Adrenaline levels during HE and control treatment were comparable at all times.
Noradrenaline concentrations peaked at 387 (95% CI 349, 425) pg/ml during HH at t = 30 min, representing a marked increase compared with both control (223 [95% CI 185, 261] pg/ml; p < 0.001) and HE (259 [95% CI 221, 298] pg/ml; p < 0.001; data not shown). There was no difference in noradrenaline concentrations during control treatment and HE at t = 30 min (p = 0.17). Noradrenaline concentrations decreased during HH to 285 (95% CI 247, 323) pg/ml at t = 75 min; these were comparable to levels during HH at t = 0 min (244 [95% CI 190, 298] pg/ml; p = 0.21).
During HH, glucagon levels were higher than during HE from t = 30 min (p < 0.001) up to t = 105 min (p < 0.01), with a peak of 133 (95% CI 119, 147) pg/ml at t = 45 min (Fig. 1d). During HE, glucagon levels were reduced compared with control from t = 30 min (p < 0.01) up to t = 105 min (p = 0.01) and glucagon nadir of 34 (95% CI 28, 39) pg/ml was observed at t = 60 min (p < 0.001). During control treatment, mean glucagon levels remained unaltered at approximately 50 pg/ml.
During HH, a glucose nadir of 2.0 (95% CI 1.7, 2.4) mmol/l was reached at t = 25 min, whereas the glucose level during HE at the same time point was 5.3 (95% CI 4.9, 5.6) mmol/l (p < 0.001; Fig. 1e).
During HH and HE, NEFA levels were reduced to an equal degree at t = 15 min: HH, 131 (95% CI 87, 198) μmol/l; HE, 151 (95% CI 97, 234) μmol/l (p = 0.4; Fig. 1f). Thereafter, NEFA levels increased steadily during HH to reach a peak of 584 (95% CI 455, 751) μmol/l at t = 105 min, approximately four times higher than during HE (140 [95% CI 89, 220] μmol/l; p < 0.001). During HE, a NEFA nadir of 66 (95% CI 45, 99) μmol/l was reached at t = 45 min.
During HH, 3-OHB levels were comparable with those during HE at t = 45 min (p = 0.44), but were higher at t = 75 min (p = 0.02) and t = 105 min (p < 0.001; Fig. 1g). During control treatment, 3-OHB levels were higher than those during HH at t = 45 min (p < 0.001) and t = 75 min (p < 0.001), but comparable with those during HH at t = 105 min (p = 0.27) and were higher than those during HE at t = 45, 75 and 105 min (p < 0.001).
A comparison of peak lactate levels during HE (t = 30 min) and during HH (t = 45 min) revealed higher levels during HH, with a mean difference of 0.66 (95% CI 0.32, 1.00) mmol/l (p < 0.001; Fig. 1h). During control treatment, mean lactate levels remained unaltered throughout the study day at approximately 0.77 (95% CI 0.59, 0.94) mmol/l.
Lipid oxidation rates
Similar to palmitate fluxes, lipid oxidation rates at 90–105 min were decreased during HE compared with both control treatment and HH (both p < 0.01). Lipid oxidation rates were comparable during both HH and control treatment: HE, 946 (95% CI −1153, 3046) kJ/day; control, 3754 (95% CI 1631, 5876) kJ/day; HH, 3011 (95% CI 870, 5152) kJ/day; p = 0.19; Fig. 2b)
Gene expression, protein modification and total protein levels
PKA phosphorylation of PLIN1
HSL Ser552 phosphorylation
At t = 30 min, the p-Ser552 HSL/total HSL ratio was 3.6-fold (95% CI 2.6-fold, 5.0-fold) higher for HH than for control treatment (p < 0.001) and 2.9-fold (95% CI 2.1-fold, 4.1-fold) higher for HH than for HE (p < 0.001; Fig. 3b). There was no difference between HE and control treatment (p = 0.22). At t = 75 min, the fold differences in HSL Ser552 phosphorylation between interventions diminished, but were still significant between HH and control treatment (1.9 [95% CI 1.3, 2.6]; p < 0.001) and between HH and HE (2.1 [95% CI 1.5, 2.9]; p ≤ 0.001).
HSL Ser650 phosphorylation
At t = 30 min, the p-Ser650 HSL/total HSL ratio was 2.4-fold (95% CI 1.6-fold, 3.8-fold) higher for HH than for control treatment (p < 0.001) and 3.4-fold (95% CI 2.2-fold, 5.3-fold) higher for HH than for HE (p < 0.001; Fig. 3c). There was no significant difference between HE and control treatment (p = 0.16). At t = 75 min, the differences were lower but the fold increase in phosphorylation was still significantly higher during HH than during control treatment (1.8-fold [95% CI 1.2-fold, 2.8-fold]; p < 0.01) and HE (1.6-fold [95% CI 1.1-fold, 2.6-fold]; p = 0.03). However, no differences were detected between control treatment and HE (p = 0.68).
No differences were seen among treatments in the levels of total ATGL at t = 30 min or at t = 75 min (Fig. 3d).
Akt Ser473 phosphorylation
mTOR Ser2448 phosphorylation
At t = 30 min, the p-Ser2448 mTOR/total mTOR ratio was 2.6-fold (95% CI 2.0-fold, 3.2-fold) higher during HH compared with control (p < 0.001) and 2.4-fold (95% CI 1.9-fold, 2.9-fold) higher during HE compared with control (Fig. 4b). No significant differences were detected between HH and HE (p = 0.1). At t = 75 min, the differences were smaller, but still present: the ratio was 1.7-fold (95% CI 1.4-fold, 2.2-fold) higher during HH compared with control (p < 0.001) and similarly 1.7-fold (1.4-fold, 2.1-fold) higher during HE compared with control (p < 0.001). No differences were detected between HH and HE at this time point (p = 0.8).
At t = 30 min, the level of G0S2 gene expression was 1.5-fold (95% CI 1.1-fold, 2.1-fold) higher during HH compared with control (p = 0.01) and 1.6-fold (95% CI 1.1-fold, 2.2-fold) higher during HE compared with control (p < 0.01; Fig. 4c). No differences were detected between HH and HE (p = 0.67). At t = 75 min, the level of G0S2 gene expression was 1.9-fold (95% CI 1.3-fold, 2.6-fold) higher during HH compared with control and 1.9-fold (95% CI 1.3-fold, 2.7-fold) higher during HE compared with control. No differences were detected between HH with HE (p = 0.82).
Other proteins and genes
No significant differences in the levels of total CGI-58-protein and in the p-Thr172 AMPK/AMPK ratio were observed at t = 30 min or t = 75 min. Neither did we observe any differences in levels of CGI-58 or ATGL mRNA at these time points (data not shown).
Our study was designed to determine the increase in lipolysis rate during acute insulin-induced hypoglycaemia and whether an increase in lipolysis is reflected in activation of pro-lipolytic signalling in AT. In contrast to HE, HH induced a gradual increase in plasma NEFA and 3-OHB concentrations starting from 15 min and 45 min, respectively. Furthermore, we found an approximate threefold increase in whole body palmitate lipolysis at t = 105 min and lipid oxidation rates close to control values at t = 105 min. These findings suggest that activation of lipolysis occurs rapidly and that lipids are eventually restored to the position of major oxidative fuel. In line with these findings, we observed a robust 14-fold increase in AT PKA-mediated PLIN1 phosphorylation and a threefold increase in pro-lipolytic HSL phosphorylation at 30 min post insulin injection during HH compared with HE. Notably, this activation occurred in the presence of unaltered insulin-induced mTOR phosphorylation, unaltered G0S2 mRNA expression and augmented Akt phosphorylation, suggesting that the activation of β-adrenergic signals overrides intact insulin signals during hypoglycaemia. From a clinical point of view, these findings place activation of lipolysis high in the counter-regulatory response hierarchy and have implications for a large number of patients with diabetes and a smaller number of patients with spontaneous or reactive hypoglycaemia. It remains uncertain whether patients with diabetes and/or recurrent hypoglycaemia have intact lipolytic responses to hypoglycaemia and to what extent these responses may be compromised in hypoglycaemia-associated autonomic failure.
Experimental insulin-induced hypoglycaemia can be achieved in a variety of ways. For example, insulin can be continuously infused and glucose concentrations can be manipulated by varying the rate of exogenously administered glucose to accomplish a desired glucose level during a hyperinsulinaemic–hypoglycaemic clamp [7, 10, 11, 20]. This allows the gradual control of changes in glycaemia at close to steady-state conditions, but also involves massive insulin exposure over a long period of time. Alternatively, the hyperinsulinaemic–hypoglycaemic clamp technique can be combined with manipulating hormonal responses and metabolic processes with inhibitors such as adrenergic blockers, somatostatin and the nicotinic acid derivative Acipimox. Our study used a bolus injection of 0.1 IU insulin/kg body mass to provide a clearly defined stimulus to AT and avoid prolonged tissue exposure to insulin. It is likely that, in general, clinically occurring hypoglycaemia in insulin-treated individuals may differ from both bolus insulin administration and continuous i.v. insulin administration in terms of the insulinaemia pattern, rate of glucose excursions, possible autonomic failure, antecedent hypoglycaemia, exercise and food ingestion, all of which may affect the counter-regulatory responses. Nonetheless, we succeeded in establishing three well-controlled experimental situations: one in which glucose levels were close to normal and suppressed lipolysis (HE); a second with hypoglycaemia (glucose nadir of 2 mmol/l), clear-cut stress hormone responses and stimulation of lipolysis (HH); and a third reflecting the basal post-absorptive state (control).
Studies have consistently demonstrated that 2–3 h after the induction of hypoglycaemia, NEFA levels, 3-OHB levels and lipid oxidation rates are restored to above basal levels and that increased lipolysis therefore seems to play a pivotal role in mediating hypoglycaemia-associated counter-regulation and insulin resistance [10, 11]. To our knowledge, only one study has investigated lipolytic rates during hypoglycaemia in humans; this somewhat surprisingly reported unchanged [14C]palmitate lipolytic fluxes . However, it should be noted that only five volunteers were included, only a modest extent of hypoglycaemia was achieved (2.8 mmol/l) and insulin levels were substantially higher during hypoglycaemia than during euglycaemia. It is plausible that the latter factor independently reduced palmitate fluxes. In our study, we observed a clear increase of more than twofold in the palmitate flux at 60–105 min after insulin administration. The glucose nadir and peak adrenaline responses occurred approximately 30 min after insulin administration, whereas glucagon responses were slightly later. We also confirmed that blood NEFA concentrations, palmitate fluxes and lipid oxidation rates were similar to control levels at the end of the study. In this context, it is important to consider that, in principle, measurements of lipolytic fluxes and lipid oxidation rates rely on steady-state or ‘quasi’ steady-state conditions. The possibility that rates of lipolysis and ketogenesis were increasing during HH 60–105 min after insulin administration cannot be ruled out. On the other hand, we found that levels of specific activity reach a plateau from 90 to 105 min and, even in the presence of major changes in the rates of NEFA appearance, it has been shown that steady-state equations yield the best estimates of actual appearance rates . The observation that hypoglycaemia leads to increased rates of lipolysis is supported by a study that used continuous infusions of [9,10-3H2]palmitate in sheep .
Lipolysis is regulated by three lipases (ATGL, HSL and MAGL) which hydrolyse triacylglycerol to NEFAs and glycerol and are regulated by complex interplay among a number of pro- and anti-lipolytic intracellular agents . The most prominent effects of HH on AT signalling were a marked stimulation of PKA-dependent phosphorylation on perilipin and similar increases in HSL Ser552 and Ser650 phosphorylation, all indicative of increased β-adrenergic pro-lipolytic signalling. During HE, insulin alone more than halved PKA activity toward perilipin, whereas during HH with concomitant spikes of adrenaline, PKA activity toward perilipin more than doubled compared with control at 30 min (these differences persisted to t = 75 min). Our findings of persistent increases in HSL Ser552 and Ser650 phosphorylation of more than twofold at t = 30 and t = 75 min suggest a strong stimulation of PKA activity toward perilipin and HSL.
It has been demonstrated that ATGL is phosphorylated at Ser406 by AMPK in mice  and that ATGL Ser406 is phosphorylated by PKA, leading to increased ATGL activity . It has also been demonstrated that ATGL Ser404 phosphorylation in human AT explants (corresponding to Ser406 in mice) is increased by β-adrenergic stimulation and corresponds to increased lipolysis rates . Thus, it is plausible that ATGL activation by PKA contributes to the enhanced lipolysis during hypoglycaemia observed in our study. There is, however, a lack of a reliable measure of ATGL activity, which could have confirmed this finding.
Furthermore, we found that Akt phosphorylation was rapidly stimulated by insulin and actually increased during hypoglycaemia at t = 30 min. This finding, together with comparable levels of mTOR phosphorylation during HE and HH and similar 50–100% increments in G0S2 mRNA levels, suggests that the anti-lipolytic insulin signal remains intact during HH [14, 29, 30]. It should be noted that insulin and C-peptide levels from t = 30 min onwards were modestly increased during HE (reflecting relative hyperglycaemia), leading to increased endogenous insulin release during the euglycaemic clamp. This increase, however, did not alter insulin signalling in AT, which appears to be primarily triggered by the initial very high spike concentrations of insulin.
It is unlikely that other counter-regulatory hormones significantly contribute to the rapid stimulation of lipolysis during hypoglycaemia. Although both GH and cortisol have lipolytic activity, this only becomes apparent after a latency of more than 1–2 h [31, 32].
Our data show that insulin-induced hypoglycaemia rapidly activates lipolysis and restores rates of lipolysis to close to basal values within 60–105 min, thus mobilising alternative fuel sources and contributing to NEFA-induced insulin resistance. These rapid effects appear to be mediated by the stimulation of PKA activity and pro-lipolytic HSL phosphorylation, compatible with the activation of β-adrenergic catecholamine signalling, to override insulin inhibition of lipolysis in AT.
We would like to thank A. Mengel, K. Nyborg Rasmussen, E. Søgaard Hornemann and K. Mathiassen of the Medical Research Laboratories, H. Zibrandtsen of the Research Laboratories for Biochemical Pathology and L. Pedersen of the Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Denmark, for their excellent technical assistance.
This study was supported by Aarhus University, the Novo Nordisk Foundation and the KETO Study Group/Danish Agency for Science Technology and Innovation (grant no. 0603–00479, to NM).
Duality of interest statement
The authors declare that there is no duality of interest associated with this manuscript.
NM, MHV, TSV and UK designed the study; TSV recruited the participants; TSV conducted the trial; NJ, NM, MJ, MVS, SBP, TSN and TSV collected the data; TSV conducted the statistical analyses; NM and TSV wrote the manuscript; and NJ, MJ, MHV, MVS, SBP, TSN, UK reviewed and edited the manuscript. NM is the guarantor of this work. All authors approved the final version of the manuscript.
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