Short Hypoxia Does not Affect Plasma Leptin in Healthy Men under Euglycemic Clamp Conditions

Schmoller, Andre; Voss, Michaela; Gehring, Hartmut; Rudolf, Sebastian; Schweiger, Ulrich; Schultes, Bernd; Oltmanns, Kerstin M.

doi:https://doi.org/10.1155/2009/270698

International Journal of Endocrinology

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Research Article | Open Access

Volume 2009 | Article ID 270698 | https://doi.org/10.1155/2009/270698

Short Hypoxia Does not Affect Plasma Leptin in Healthy Men under Euglycemic Clamp Conditions

Andre Schmoller,¹Michaela Voss,¹Hartmut Gehring,²Sebastian Rudolf,¹Ulrich Schweiger,¹Bernd Schultes,³and Kerstin M. Oltmanns^1,4

Academic Editor: Graeme Eisenhofer

Received15 Jan 2009

Accepted12 Mar 2009

Published01 Jun 2009

Abstract

Leptin is involved in the endocrine control of energy expenditure and body weight regulation. Previous studies emphasize a relationship between hypoxic states and leptin concentrations. The aim of this study was to investigate the effects of acute hypoxia on leptin concentrations in healthy subjects. We examined 14 healthy men. Hypoxic conditions were induced by decreasing oxygen saturation to 75% for 30 minutes. Plasma leptin concentrations were determined at baseline, after 3 hours of euglycemic clamping, during hypoxia, and repeatedly the following 2.5 hours thereafter. Our results show an increase of plasma leptin concentrations in the course of 6 hours of hyperinsulinemic-euglycemic clamping which may reflect diurnal rhythmicity. Notwithstanding, there was no difference between levels of leptin in the hypoxic and the normoxic condition (). Since we did not find any significant changes in leptin responses upon hypoxia, plasma leptin levels do not seem to be affected by short hypoxic episodes of moderate degree.

1. Introduction

Hypoxia is suggested to play an important role in the pathogenesis of endocrine and metabolic dysregulation in obesity and the metabolic syndrome [1]. We could previously demonstrate, based on an experimental human in vivo design established in our group, that 30 minutes of oxygen desaturation to 75% are sufficient to induce features of the metabolic syndrome such as glucose intolerance [2, 3] and respective changes in sympathetic activation [2, 3], resting energy expenditure [2, 3], and vascular endothelial growth factor (VEGF) levels [4], a hormone which has been assumed to play a role in the pathogenesis of the metabolic syndrome [5].

Another hormone centrally involved in body weight regulation and thereby the development of the metabolic syndrome is leptin [6]. Leptin is synthesized mainly, but not exclusively, by white adipose tissue sending a feedback signal to the brain about the amount of peripheral fat storages. The secretion of leptin underlies various influencing factors. Recent literature indicates that circulating leptin concentrations are possibly increased by hypoxic conditions in humans, suggesting a link to the obstructive sleep apnea syndrome (OSAS), a disease characterized by recurrent night apneic periods, which is strongly associated with obesity [7]. Indeed, as compared to healthy controls, OSAS patients show elevated leptin concentrations which return to normal after elimination of night apneas by continuous positive airway pressure (CPAP) therapy [8]. However, it remains unclear if high leptin levels in these patients are related to hypoxia, to hormonal interactions, or to the frequently increased body mass in OSAS. At high altitude (3000–4000 m), that is, under constant hypoxic conditions, increased [9, 10] as well as decreased leptin concentrations [11] have been reported in humans as compared to sea level. Potential confounders of leptin secretion in this setting are physical strain, nutritional differences, or physical stress upon ascension. Previous studies using cell cultures [12–14] and animal models have provided [15] a contradicting evidence for an impact of hypoxia on leptin concentrations.

In order to clarify if hypoxia affects circulating leptin concentrations in humans, we experimentally induced a short hypoxic period as compared to normoxic condition in healthy normal weight participants according to our established study design which has been demonstrated to induce clinically relevant changes in energy and hormone metabolism [2, 3]. Oxygen saturation of 75%, as applied in our study, corresponds to a physiological state at approximately an altitude of 3500–4000 m. To control for common biases known to influence leptin metabolism, we performed our study at rest. Moreover, our group has previously shown that the glucose metabolism is a main determinant of leptin secretion [16, 17]. Each subject, therefore, underwent an euglycemic glucose clamp procedure to ensure stable circulating glucose and insulin concentrations throughout the experiments to control for these influencing factors on plasma leptin levels. Additionally, sympathetic activation as evaluated by circulating epinephrine and norepinephrine concentrations was monitored.

2. Methods and Procedures

2.1. Subjects

Experiments were performed including 14 healthy men aged 20–25 years. Exclusion criteria were overweight (body mass index (BMI) 25 kg/), chronic or acute illness (particularly respiratory diseases), alcohol or drug abuse, smoking, competitive sports, exceptional physical or mental stress, and current medication of any kind. Each participant gave a written informed consent, and the study was approved by the local ethics committee.

2.2. Experimental Design

Subjects participated in a hypoxic and a normoxic session separated by an interval of at least 4 weeks. Hyperinsulinemic-euglycemic clamp procedures were performed during the entire experimental testing. A detailed clamping procedure has been described previously [2, 17]. Subjects were blinded for conditions.

On the days of experimental testing, subjects reported to the medical research unit at 11:00 h after an overnight fast of at least 12 hours. After 3 hours of clamping, hypoxia was induced for 30 minutes by decreasing oxygen saturation to 75%. On the normoxic control condition, oxygen saturation was held at the physiological level of 98%. We assessed the course of leptin concentrations at baseline and repeatedly 3 hours after induction of hypoxia according to leptin’s half life in normal weight men of about 3 hours by punctional determination [18]. During induction of hypoxia and also during the normoxic control period, participants breathed at normobaric conditions through a tightly fitting face mask connected to a Trajan 808 fresh gas supply (Draeger Medical Technology, Luebeck, Germany), using a valveless high-flow system between 14 and 17 l/min. Inspired oxygen fraction was varied by adjusting oxygen and nitrogen. Oxygen saturation was continuously measured by pulse oxymeter and was decreased to 75% within approximately 5 minutes. After 30 minutes, oxygen saturation was quickly normalized. Catecholamine levels were monitored at baseline and every 7.5 minutes during hypoxia (versus control).

2.3. Assays

All blood samples were immediately centrifuged and the supernatants stored at until assay. Leptin concentrations were measured by ELISA (Diagnostic Systems Laboratories, Sinsheim, Germany; interassay coefficient of variation (CV) 4.4%, intra-assay CV 3.8%). Serum insulin was measured by radioimmunoassay (Pharmacia Insulin RIA 100, Pharmacia Diagnostics, Uppsala, Sweden; inter-assay coefficient of variation (CV) 5.8%, intra-assay ). Blood glucose concentrations were monitored at 5-minute intervals throughout the experiment (Glucose Analyser, Beckman Coulter, Inc. Munich, Germany). High pressure liquid chromatography was applied to measure plasma epinephrine (intra-assay ; inter-assay ) and norepinephrine levels (intra-assay ; inter-assay , Chromosystems, Munich, Germany).

2.4. Statistical Analysis

Values are presented as mean values SEM. Analyses of variance (ANOVA) for repeated measurements, including the factors “session” (hypoxia versus normoxia) and “time” (time points of data collection) were implemented and corrected according to the Greenhouse-Geisser procedure. The interaction effect of these two factors was termed “session by time.” The area under the curve (AUC) was calculated from 6 hours leptin short-profiles to determine overall differences in leptin secretion between the two sessions. In addition, student’s paired -tests were performed to compare hormone concentrations at single time points. A -value .05 was considered significant.

3. Results

3.1. Oxygen Saturation, Serum Insulin, Plasma Glucose, and Catecholamines

Upon induction of hypoxia, oxygen saturation decreased over a period of about 5 minutes and was held stable at a plateau of . Oxygen saturation (corresponding to 35–41 mmHg PaO2) during the corresponding period under the normoxic condition remained at a mean level of . Determination of plasma glucose concentrations and serum insulin confirmed that respective blood levels remained constant after having reached the equilibrium and did not differ between hypoxic and normoxic conditions throughout the study (Figure 1). Also, as already published [3], norepinephrine concentrations did not differ significantly between the two sessions () whereas epinephrine levels were significantly higher under the hypoxic condition as compared with the control session (). The glucose infusion rates were significantly lower during the hypoxic as compared to the normoxic period [2].

(a)

(b)

3.2. Plasma Leptin Concentrations

Figure 2 shows the course of leptin concentrations during normoxic and hypoxic conditions under euglycemia. Overall, leptin levels increased significantly during hypoxia () and normoxia () in the overall time course of 6 hours of measurements. There were no statistical differences in leptin levels between hypoxic and normoxic conditions as revealed by ANOVA for repeated measurements for the “session” effect () and the interaction effect (). Analyses of the AUCs of leptin concentrations confirmed that there was no difference between the two conditions (). Paired -test comparison revealed that there were no differences between the groups at baseline (). Similarly, after having reached the euglycemic equilibrium, plasma leptin concentrations showed no significant differences between conditions directly before the induction of hypoxia, during the hypoxic period, and during the 2.5 hours period after hypoxia in -test comparison of single time points ( for all).

(a)

(b)

4. Discussion

Our results show that plasma leptin concentrations are not affected by acute hypoxia as compared to normoxic control in healthy subjects at rest. In contrast, previous studies showed an inverse correlation of serum leptin levels to altitude [11, 19, 20], that is, when altitude increase serum leptin levels drop. However the effects of hypoxia on circulating leptin concentrations are contradicting as recently discussed in detail by Sierra-Johnson et al. [21–23].

The underlying cause why our results do not confirm previous data indicating an increasing effect of hypoxia on leptin levels deserves to be explained. One reasoning may be based on hormonal influences. Norepinephrine and epinephrine have been shown to inhibit leptin secretion [24–26], whereas glucocorticoids, for example, dexamethasone, stimulate leptin secretion in humans [27, 28]. So it may be speculated that in our study a potential increase in leptin concentrations upon hypoxia may be masked by suppressing effects of the risen epinephrine levels under this condition. This mechanism, however, can only remain speculation within the scope of an in vivo approach as applied here and requires some confirmation in further studies.

Our second finding was a significant increase in leptin concentrations in the course of the six hours of the experimental procedure. This is in line with the finding that circulating leptin concentrations display ultradian and circadian rhythmicity with a nadir about noon and the early afternoon, and peak levels during the night [29, 30]. The increase in leptin concentrations starting prenoon and the following 6 hours as reported here may reflect this diurnal variation. Moreover, the increased leptin concentrations may also be due to the standardized insulin infusion during the clamp [16, 17, 31]. Since insulin has been shown to elevate leptin concentrations [17, 32], we intended to exclude this biasing factor by applying the hyperinsulinemic-euglycemic clamp technique which adjusts constant insulin concentrations during the experiments. Notwithstanding, this method may have contributed to the overall rise in leptin levels even though in all conditions equally.

One central question we intended to focus by our study was if alterations in leptin concentrations in OSAS patients could be assigned either to recurrent hypoxia or to the known high BMI which is a frequently found feature in this disease. Generally, leptin is produced by white adipose tissue and downregulates food intake by inhibiting neuropeptide Y synthesis and elevating alpha-melanocyte stimulating hormone synthesis in the hypothalamus, a feedback mechanism signalling increased peripheral fat reserves to cerebral appetite centers [33]. Indeed, it has been shown that serum leptin levels are positively correlated with the BMI [33, 34]. Remarkably, some studies could demonstrate that OSAS patients, however, display higher leptin levels than BMI-matched obese and normal weight subjects [34, 35]. Since Leptin is a physiological feedback signal to reduce appetite and thereby should prevent the development of obesity, the occurrence of overweight and elevated circulating leptin concentrations, as seen in OSAS patients, deserves an explanation. There are two possible mechanisms conceivable. One possible explanation is a congenital leptin deficiency, although this is a rarely seen defect [36]. The second avowal could be a relative leptin resistance, due to the fact that leptin seems to downregulate its own receptors, so high leptin levels could possibly reduce the number of leptin receptors and generate a relative leptin resistance which in turn causes obesity [37]. On the other hand, it was demonstrated that the apnea-hypopnea index (AHI) correlates positively with serum leptin concentrations in patients with OSAS but not in the BMI-matched control group and there was a significant decrease of serum leptin levels in OSAS patients upon treatment with CPAP therapy over six months despite of stable BMI values [34, 38]. Therefore, we can speculate that recurrent oxygen desaturations in OSAS patients may play a major role in the regulation of leptin concentrations disregarding the influence of obesity. Notwithstanding, our data do not confirm the hypothesis that elevated leptin concentrations in OSAS patients are caused by hypoxia either. This negative result, however, may be based on our study protocol which fundamentally differs from the approach of other investigations. Our subjects underwent only a single moderate hypoxic episode of 30 minutes in length. This hypoxic pattern differs from previous studies according to length, frequency, and degree of oxygen desaturation [8, 9, 11, 12]. Zaccaria et al., for example, studied male subjects at high altitude with an observation period of 20 days [11]. Therefore, it remains to be carefully considered to what extent our findings can be assigned to the hypoxic conditions as present in OSAS where severe hypoxic periods, displaying distinctly lower oxygen saturation values than 75%, can be observed [8]. So eventually our negative findings may simply reflect an insufficient duration and the extent of hypoxia to affect leptin secretion. Notwithstanding, our study design has been established to induce clinically relevant changes in other features of the metabolic syndrome [2, 3] and is therefore an adequate approach to gain first insight into the effects of acute hypoxia in this context in humans. In addition, this is the first study investigating the effects of acute hypoxia on leptin concentrations controlling for fundamental influencing factors in healthy men. According to our data, plasma leptin levels seem to be unaffected by short hypoxic episodes of moderate degree. Future studies are desirable to further clarify the relationship between hypoxia and leptin regulation in physiological and pathophysiological states.

Acknowledgments

We thank Christiane Otten for her expert and laboratory assistance and Anja Otterbein for her organizational work. None of the authors reported any disclosures.

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Copyright © 2009 Andre Schmoller et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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