|A natural variant of obestatin, Q90L, inhibits ghrelin's action on food intake and GH secretion and targets NPY and GHRH neurons in mice.|
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|PMID: 23251435 Owner: NLM Status: MEDLINE|
|BACKGROUND: Ghrelin and obestatin are two gut-derived peptides originating from the same ghrelin/obestatin prepropeptide gene (GHRL). While ghrelin stimulates growth hormone (GH) secretion and food intake and inhibits γ-aminobutyric-acid synaptic transmission onto GHRH (Growth Hormone Releasing Hormone) neurons, obestatin blocks these effects. In Humans, GHRL gene polymorphisms have been associated with pathologies linked to an unbalanced energy homeostasis. We hypothesized that one polymorphism located in the obestatin sequence (Q to L substitution in position 90 of the ghrelin/obestatin prepropeptide, rs4684677) may impact on the function of obestatin. In the present study, we tested the activity of native and Q90L obestatin to modulate ghrelin-induced food intake, GH secretion, cFos activity in GHRH and Neuropeptide Y (NPY) neurons and γ-aminobutyric-acid activity onto GHRH neurons.
METHODOLOGY/PRINCIPAL FINDINGS: Food intake, GH secretion and electrophysiological recordings were assessed in C57BL/6 mice. cFos activity was measured in NPY-Renilla-GFP and GHRH-eGFP mice. Mice received saline, ghrelin or ghrelin combined to native or Q90L obestatin (30 nmol each) in the early light phase. Ghrelin stimulation of food intake and GH secretion varied considerably among individual mice with 59-77% eliciting a robust response. In these high-responders, ghrelin-induced food intake and GH secretion were reduced equally by native and Q90L obestatin. In contrast to in vivo observations, Q90L was slightly more efficient than native obestatin in inhibiting ghrelin-induced cFos activation within the hypothalamic arcuate nucleus and the nucleus tractus solitarius of the brainstem. After ghrelin injection, 26% of NPY neurons in the arcuate nucleus expressed cFos protein and this number was significantly reduced by co-administration of Q90L obestatin. Q90L was also more potent that native obestatin in reducing ghrelin-induced inhibition of γ-aminobutyric-acid synaptic transmission onto GHRH neurons.
CONCLUSIONS/SIGNIFICANCE: These data support the hypothesis that Q90L obestatin partially blocks ghrelin-induced food intake and GH secretion by acting through NPY and GHRH neurons.
|Rim Hassouna; Philippe Zizzari; Odile Viltart; Seung-Kwon Yang; Robert Gardette; Catherine Videau; Emilio Badoer; Jacques Epelbaum; Virginie Tolle|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2012-12-10|
|Title: PloS one Volume: 7 ISSN: 1932-6203 ISO Abbreviation: PLoS ONE Publication Date: 2012|
|Created Date: 2012-12-19 Completed Date: 2013-06-11 Revised Date: 2013-07-11|
Medline Journal Info:
|Nlm Unique ID: 101285081 Medline TA: PLoS One Country: United States|
|Languages: eng Pagination: e51135 Citation Subset: IM|
|UMR-S 894 INSERM, Centre de Psychiatrie et Neurosciences, Université Paris Descartes, Sorbonne Paris Cité, Paris, France.|
|APA/MLA Format Download EndNote Download BibTex|
Feeding Behavior / physiology*
Ghrelin / antagonists & inhibitors*, physiology*
Growth Hormone / antagonists & inhibitors*, secretion
Growth Hormone-Releasing Hormone / metabolism*
Mice, Inbred C57BL
Neurons / metabolism*
Neuropeptide Y / metabolism*
|0/Ghrelin; 0/Neuropeptide Y; 9002-72-6/Growth Hormone; 9034-39-3/Growth Hormone-Releasing Hormone|
Journal ID (nlm-ta): PLoS One
Journal ID (iso-abbrev): PLoS ONE
Journal ID (publisher-id): plos
Journal ID (pmc): plosone
Publisher: Public Library of Science, San Francisco, USA
Copyright: 2012 Hassouna et al
Received Day: 25 Month: 6 Year: 2012
Accepted Day: 29 Month: 10 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 10 Month: 12 Year: 2012
Volume: 7 Issue: 12
E-location ID: e51135
PubMed Id: 23251435
Publisher Id: PONE-D-12-18380
|A Natural Variant of Obestatin, Q90L, Inhibits Ghrelin's Action on Food Intake and GH Secretion and Targets NPY and GHRH Neurons in Mice Alternate Title:Obestatin-Q90L Effect on Feeding and GH Secretion|
1UMR-S 894 INSERM, Centre de Psychiatrie et Neurosciences, Université Paris Descartes, Sorbonne Paris Cité, Paris, France
2UMR 837 INSERM, Laboratoire “Développement et Plasticité du Cerveau Postnatal”, Centre de Recherches JPARC, Lille and Université Lille Nord de France (USTL- Lille 1), Lille, France
3School of Biomedical Sciences, The University of Queensland, Skerman Building (65), St Lucia, Queensland, Australia
4School of Medical Sciences and Health Innovations Research Institute, RMIT University, Bundoora, Melbourne, Victoria, Australia
|CRCHUM-Montreal Diabetes Research Center, Canada
|Correspondence: * E-mail: email@example.com
[conflict] Competing Interests: The authors have declared that no competing interests exist.
Contributed by footnote: Conceived and designed the experiments: RH VT. Performed the experiments: RH PZ OV SY CV EB. Analyzed the data: RH PZ SY RG JE VT. Contributed reagents/materials/analysis tools: PZ OV. Wrote the paper: RH VT. Revised the manuscript: JE.
Ghrelin is a 28 amino acid peptide principally synthesized in the stomach and was originally described as the endogenous ligand of the Growth Hormone Secretagogue 1a Receptor (GHS-R1a) , . Ghrelin is the only orexigenic gastrointestinal peptide and one of its main functions is to stimulate growth hormone (GH) secretion , . Binding of ghrelin to the GHS-R1a, which relays most of ghrelin's biological effects, is made possible due to a post-translational acylation on its serine in position 3 , . GHS-R1a is highly expressed in the arcuate nucleus (ARC) of the hypothalamus, a key region involved in the control of GH secretion and appetite but also in the brainstem that receives information from gut vagal afferents , . Within the hypothalamus, ARC Neuropeptide Y (NPY) and Growth Hormone Releasing Hormone (GHRH) neurons express the GHS-R1a , , and are a well-characterized target for ghrelin or GHS actions –. More recently, obestatin, a 23 amino acid peptide, derived from the cleavage of preproghrelin was discovered  and reported as an anorexigenic peptide ligand of the orphan receptor, GPR39, but these findings are controversial –. Nevertheless, when co-administered with ghrelin at equimolar doses, obestatin counteracts, for instance, ghrelin induced food intake and GH secretion in rodents . The mechanism of action of obestatin and its interaction with ghrelin in the central nervous system remain poorly understood. The effect of obestatin on ghrelin-induced GH secretion is not mediated at the pituitary level , , suggesting that the interaction between ghrelin and obestatin is mainly mediated within the central nervous system. Indeed, recently, it was reported that obestatin blocks ghrelin-induced inhibition of γ-aminobutyric acid (GABA) synaptic transmission onto GHRH neurons .
In humans, ghrelin/obestatin prepropeptide gene (GHRL) polymorphisms have been associated with pathologies linked to an unbalanced energy homeostasis like anorexia or bulimia nervosa , . One of those single nucleotide polymorphisms (SNP) (Q to L substitution in position 90 of preproghrelin, rs4684677) is located in the sequence encoding obestatin and anorexic patients carrying this SNP have a lower minimum body mass index (BMI) . This polymorphism may thus influence the function of obestatin.
In this study, we compared the effect of native and Q90L obestatin in modulating ghrelin-induced food intake and GH secretion. These two parameters were measured after co-administration of the peptides in the light phase in ad libitum fed C57BL/6 mice. To define the central sites of interaction of these peptides, we assessed neuronal activation after co-administration of ghrelin and native or Q90L obestatin, in two key regions involved in regulation of GH secretion and/or food intake: the ARC in the hypothalamus and the NTS in the brainstem. Moreover, we investigated whether ghrelin and obestatin interacted directly on ARC NPY and GHRH neurons which relay ghrelin effects on food intake and GH release respectively , –.
The ability of human obestatin (hOb) and hObQ90L to inhibit ghrelin-induced food intake and GH secretion was tested after administration of equimolar doses (30 nmol ip) of ghrelin and hOb or hObQ90L during the light period in male C57BL/6 mice (Figure 1). We observed a high variability in the responses to peptides injections in individual mice and only a proportion responded to stimulation by ghrelin. Based on these observations, we determined a threshold to classify ghrelin-treated animals into either high or low responders. This was possible because each mouse was injected with each treatment in a cross-over designed manner. For food consumption, the threshold was defined as the mean value+3 standard deviations (SD) measured during 0–4 h after saline injection. For GH secretion, the threshold was defined as the mean value+3 standard deviations (SD) of the peak value recorded.
Fifty nine percent of mice increased their food consumption over a threshold of 0.42 g (high responders) 4 hours after ghrelin injection whereas 41% of mice did not (low responders) (Figure 1A). For GH secretion, 75% of mice exceeded the calculated threshold of 143 ng/ml (high responders) (Figure 1B). After co-administration of ghr+hOb or ghr+hObQ90L, the profile of the distribution of the responses was similar between high and low responders (Figure 1A and B). There was no difference between the two forms of obestatin in reducing the ghrelin-induced food intake or GH secretion when all animals were included.
Based on the above observations, the results for food intake and GH secretion were analyzed separately in high and low responders, the latter being shown in the Supporting Information.
Feeding behavior was monitored after Ghr and/or after co-administration of Ghr+hOb/hObQ90L in male C57BL/6 mice. In high responders only, hOb and hObQ90L attenuated the ghrelin-induced cumulative food intake within 4 hours following treatments and the activity of the two forms of obestatin was equivalent (Figure 2A). Within the first hour following the injection, however, neither hOb nor hObQ90L inhibited the effects of ghrelin.
The analysis of the meal pattern revealed that the inhibitory effect of both forms of obestatin was due to a decrease in meal size and duration (Figure 2B–D). The effect of hObQ90L appeared to be slightly more pronounced than hOb more particularly in reducing ghrelin's effect on total meal duration.
In low responders, although ghrelin did not elicit an increase in cumulative food consumption (Fgure 1A), mice did respond to co-administration of ghr+hOb/hObQ90L notably by increasing meal number, size and duration (Figure 1B–D). hOb or hObQ90L injected alone did not affect food intake or meal pattern (Data not shown).
The ability of hOb and hObQ90L to inhibit ghrelin-induced GH secretion was tested after administration of equimolar doses (30 nmol ip) of ghrelin and hOb/hObQ90L during the light period in both male and female mice (Figure 3). In high responders only, ghrelin induced an increase in the amplitude of GH secretion and this was significantly reduced by co-administration of Ghr+hOb but not Ghr+hObQ90L 20 minutes following the injection only (Figure 3A). Due to the inter-individual variability in all groups, the area under the curve (AUC) analysis showed a small inhibitory effect of both forms of obestatin although not statistically different from the ghrelin group (Figure 3B). There was no significant difference observed in the responses to the two forms of obestatin. In low responders, no statistical differences were observed between treatments (Figure 2).
cFos immunoreactive cells were quantified from 2.2/1.6 mm of the interaural line for the ARC and from −3.78/−3.98 mm of the interaural line for the NTS. Representative micrographs are illustrated on Figure 4A and C for ARC and NTS respectively. The increased number of cFos immunoreactive cells after ghrelin injection was significantly reduced by hObQ90L in both ARC (Figure 4B) and NTS (Figure 4D). The effects of both human (hOb) and rat (rOb) obestatin on cFos activation were pooled as no differences were observed between both forms (data not shown).
GFP positive cell number was quantified from 2.2/1.6 mm of the interaural line in the ARC. The number of GFP-positive neurons did not differ between the treatment groups (Figure 5A and Table S1). Ghrelin induced a significant increase in the number of NPY neurons expressing cFos compared to saline-injected animals (26% vs 2% of NPY neurons, respectively) (Figure 5B). In NPY neurons, co-localization with cFos was reduced significantly to 11% with hObQ90L but not with hOb (Figure 5A). Only 8% of GHRH neurons expressed cFos following ghrelin (Table S1). This was not significantly different from controls due to the lower proportion of ghrelin-activated neurons and the inter-individual variability.
Because ghrelin has been shown to reduce GABA synaptic transmission to GHRH neurons, evoked GABA synaptic responses were recorded in GHRH neurons expressing GFP. Both native and hObQ90L obestatin dose-dependently inhibited ghrelin effects on GABA transmission (Figure 6). hObQ90L obestatin was 2.5 times more potent in inhibiting the ghrelin-induced decrease of evoked GABA synaptic response in GHRH neurons (EC50 18 µM for hObQ90L and 66.4 µM for hOb).
In the present study, we observe that a natural variant of human obestatin, hObQ90L, is slightly more active than the native peptide to suppress some of ghrelin's biological effects in mice that respond to ghrelin. Indeed, only 59% and 75% of ghrelin-treated mice responded to ghrelin's actions on food intake and GH secretion, respectively. To our knowledge, this is the first report showing that i.p injection of ghrelin does not always lead to a major increase in food consumption or GH secretion. As the effects of obestatin can only be observed in high responders, inter-individual heterogeneity in ghrelin responses may explain why several studies failed to see any inhibitory action of obestatin on ghrelin-induced food intake or GH secretion , . Controversy concerning the physiological significance or pharmacological actions of obestatin is partly due to the difficulty to reproduce published data and to the lack of concordant information in the literature , , , , . Thus the pharmacological action of obestatin in reducing ghrelin-induced food intake and GH secretion  appears to depend upon the ability of individual animals to respond to ghrelin. For instance, ghrelin-induced cFos activation or feeding has been shown to be different in fed and fasted states , . In the present study, we were unable to demonstrate any correlation between the food consumed within 15 minutes prior to peptides injections and ghrelin-induced feeding (R2 = 0,001, P = 0,8870). Thus, biological parameters, like nutritional status or stress level, could impact on the response to ghrelin but this remains to be demonstrated.
ObQ90L polymorphism is found in the general population with a frequency of 2–14%. Although this single nucleotide polymorphism does not appear to be associated with metabolic or eating disorders according to population studies –, anorexic patients carrying this SNP have a lower minimum body mass index (BMI) . Together with the current data, it may suggest that ObQ90L polymorphism, located in the sequence encoding for obestatin, has a stronger inhibitory action on some of the circuits regulating feeding compared to the natural peptide, which has been found to be a functional ghrelin antagonist previously , .
Although no significant difference between native and Q90L obestatin is observed on cumulative food intake over 4 hours, analysis of meal structure reveals that hObQ90L, at the dose of 30 nmol, has a slightly larger effect in reducing total meal duration than the natural peptide. Real differences in potencies between both peptides cannot be ascertained from analysis of feeding pattern as dose-responses were not performed. At any rate, the results indicate that native and Q90L obestatin partially reduce ghrelin-induced food intake by modulating satiation (i.e meal termination). A suppressive effect on the ghrelin-induced food intake is not observed within the first hour following the injection, suggesting that the inhibitory action of both native and Q90L obestatin on ghrelin-induced food intake is delayed. However in a previous study , the inhibitory effect of obestatin on the ghrelin-induced food intake was observed immediately following the injection. Such a discrepancy could be related to different experimental paradigms, injections being performed just before the dark phase in the previous study and during the light phase herein. For ghrelin-induced GH secretion, inhibition by hObQ90L is not more pronounced than native obestatin. In addition, we were unable to demonstrate an effect of obestatin per se, confirming most of previous data .
In the absence of an identified obestatin receptor and adequate tools to study obestatin function (agonists or antagonists), the mechanism of action of obestatin and its interaction with ghrelin in the central nervous system have remained poorly understood. We thus tested for the first time whether obestatin could modulate ghrelin effects by acting on the same neuronal populations synthesizing the orexigenic peptide NPY. ARC NPY neurons are a well-characterized target for ghrelin actions in the hypothalamus. In the rat, in-situ hybridization studies show co-localization between the GHS-R and NPY (and GHRH) mRNAs , . In addition, intravenous administration of GHRP-6, a synthetic GHS, activates cFos in GHRH and NPY neurons: around half of the activated cells are NPY containing and around one quarter are GHRH containing cells . Here, we describe for the first time by using NPY-Renilla-GFP mice that i.p administration of ghrelin activates 26% of NPY neurons in the ARC while 53% of cFos immunoreactive cells are GFP positive. This is consistent with previous results showing that a majority of cFos immunoreactive cells after i.p injection of ghrelin express NPY mRNA in mice . The proportion of NPY neurons expressing cFos is robustly reduced from 26 to 11% by Q90L obestatin, demonstrating that the actions of this natural variant are relayed through this population of orexigenic neurons. In addition, the activation of NTS neurons, another target of ghrelin, is also more reduced by Q90L obestatin than with the native peptide. As the NTS relays information about satiety and satiation, these data are consistent with an effect of obestatin on ghrelin-induced increase in meal size and duration.
Only a small proportion of GHRH-eGFP neurons were activated by ghrelin treatment in the current study (8% of GHRH-eGFP neurons are cFos positive). Consequently, a significant inhibitory action of obestatin on GHRH neurons using cFos quantification could not be demonstrated, despite the fact that GHRH neurons express the GHS-R ,  and GHRH does play a role in ghrelin-induced GH secretion in rats . In addition, this contrasts with data obtained in rats showing that the synthetic GHSs, GHRP-6 and KP-102, activate cFos in a significant number of GHRH neurons, although the proportion of GHRH cells expressing cFos mRNA was very different with both GHS (38% with GHRP-6 and 20% with KP-102) , . Thus differences in activated cells from one study to another may be due to species differences, measurement of mRNA versus GFP-positive cells or to differences in the mechanism of actions of various GHS-R ligands. A recent study from our laboratory using patch-clamp recording in mice demonstrated that ghrelin activates 44% of recorded GHRH neurons by inhibiting GABA synaptic transmission onto GHRH neurons and this was inhibited by obestatin . The discrepancies between the cFos data and single-cell recording following ghrelin stimulation may be explained by differences in the experimental conditions and techniques used (electrically induced synaptic responses after direct application of ghrelin on hypothalamic slices versus cFos activation after peripheral ghrelin administration). Thus we compared the effects of native and Q90L obestatin using patch-clamp recording and demonstrated that Q90L obestatin blocks ghrelin-induced decreases in GABA synaptic transmission more potently than native obestatin. In contrast to the behavioral and physiological observations in mice, cellular assays appear to reveal a difference between native and Q90L obestatins.
In conclusion, hObQ90L not only retains its ability to reduce ghrelin effects on food intake and GH secretion, in mice that respond to ghrelin, but it also has a stronger effect than native obestatin in inhibiting neuronal activity in key target circuits regulating feeding or GH secretion. Substitution of one amino-acid by another has previously been shown to modify the biological activity of peptides , . These results extend our knowledge about the mechanism of action of this functional ghrelin antagonist and are in keeping with clinical data showing that, in anorexic patients, this variant was more frequent amongst women with the lowest body mass index .
All experiments were carried out in accordance with the European Communities Council Directive (86/609/EEC) and were approved by the Animal Experimentation Committee of Paris Descartes University.
Adult C57Bl/6 male mice (Charles River) (11 weeks old upon arrival) were housed in individual cages for the food intake experiments. Heterozygous GHRH-eGFP transgenic mice  and NPY-Renilla GFP transgenic male and female mice  were obtained by crossing transgenic to C57Bl/6 mice. The transgenic offspring were genotyped by PCR amplification of tail DNA. All animals were housed in a room under controlled illumination (7:00 AM to 7:00 PM) and temperature (22–24°C) and had free access to food and water. All experiments were started between 9:30 AM and 10:30 AM. Male and female mice were used for GH response and immunohistochemistry experiments and only males were used for the feeding and electrophysiological experiments. No sex differences were observed.
For the food intake and GH secretion experiments, mice received an intraperitoneal (i.p) injection of saline, rat acyl-ghrelin (ghr), ghrelin+human obestatin (ghr+hob) and ghrelin+human Q90L obestatin (ghr+hobQ90L), 30 nmol each (NeoMPS Strasbourg, France). Experiments were repeated in a crossover designed manner so that each mouse received all treatments randomly separated by two days of washout. For the immunohistochemical experiments, separate groups of mice received an i.p injection of either saline, rat acyl-ghrelin, ghr+rat or human obestatin (r/hOb), or ghr+hobQ90L (30 nmol each). 90 minutes later the animals were anesthetized and perfusion-fixed (see below).
Mice were habituated to single housing and to the automated drinking/feeding station (TSE systems, GmbH, Germany) for 1 week before the beginning of the experiment. On each experimental day, mice received an i.p injection of the peptides. Feeding behavior was recorded continuously for 24 hours after the injection by means of high precision sensors, attached to the top of the cage.
Meal patterns were analyzed using the following definition: a meal consists of the consumption of 0.03 g of food separated from the next feeding episode by at least 10 minutes (intermeal interval, –). For each mouse, the meal number, the total meal size (g) and the total meal duration (minutes) were measured for 4 hours following the injection of the peptides.
Mice were habituated to single housing before the beginning of the experiment and handled in order to minimize stress. 4 µl of the whole venous blood was obtained from the tail vein every ten minutes , for one hour after the i.p injection of the peptides. Blood samples were collected in 116 µl of the Enzyme ImmunoAssay (EIA) GH buffer (PBS-0.05% tween) and kept on ice until the end of experiment and then transferred to −20°C for storage before further analysis.
Whole blood GH concentrations were evaluated by EIA as previously described .
GHRH and NPY neurons were visualized using GFP fluorescence. Specific co-localization experiments between GHRH or NPY and cFos were performed as follows. Ninety minutes after i.p injection of the peptides, the mice were anaesthetized (5.47 mg/30 g BW of sodium pentobarbital) and perfused transcardially with 0.9% saline followed by fixative containing 4% paraformaldehyde (PFA) in PB (0,1 M). The brains were removed, post-fixed in 4% PFA in PB for 2 hours at room temperature and cryoprotected in 30% sucrose for 2 days at 4°C before freezing in 2-methyl-butane (at −35°C). Serial coronal sections, 25 µm thick, were cut using a freezing microtome (Frigomobile, Leica, Wetzlar, Germany). Immunofluorescence was performed on free-floating sections, separated by 100 µm for the entire rostro-caudal extent of the hypothalamic arcuate nucleus (ARC) and the nucleus solitary tract (NTS) of the brainstem. The sections were first incubated with primary antibody: anti-cFos raised in rabbit (1∶20000, Ab-5, Jackson Laboratories, West Grove, PA, USA) and then with Cy3 conjugated donkey anti-rabbit antiserum (1∶800, Jackson Laboratories, West Grove, PA, USA). Sections were examined using a Zeiss Axioplan microscope (Carl Zeiss, Le Pecq, France). The number of cFos positive cell nuclei and GFP positive cell bodies were counted bilaterally under a 40× magnification, in ARC (interaural line: 2.2 to 1.6 mm from Paxinos and Watson's mouse brain atlas, 1997) and in the NTS (interaural line: −3.78 to −3.98 mm). GFP positive cell bodies expressing cFos were visualized using a confocal SP5 microscope (Leica, Wetzlar, Germany). The number of cells showing co-localization was determined using the Image-J software (http://rsbweb.nih.gov/ij/) on series of continuous optical sections with 0.5 µm increment along the z-axis of the section under a 40× magnification. Confocal images presented were obtained from individual optical slices.
Electrophysiological experiments were conducted as described previously . Briefly, recordings were performed at room temperature on 200 µm thick hypothalamic coronal slices from 8–13 week-old male GHRH-eGFP transgenic CB57Bl/6J placed in a bath solution containing 124 mM NaCl, 3 mM KCl, 1.25 mM NaH2PO4, 1 mM MgSO4, 2 mM CaCl2, 26 mM NaHCO3, 10 mM Glucose, 10 µM CNQX (6-cyano-7nitroquinoxaline-2,3-dione, AMPA-R antagonist) and 50 µM D-AP-5 (2-amino-5-phosphonovalerate, NMDA-R antagonist), pH 7.3, 300–310 mOsm/L, and perfused at a rate of 2 ml/minutes. GHRH-eGFP ARC neurons were visually identified by fluorescent microscopy. To record electrically induced synaptic responses, patch recording pipettes were filled with 131 mM CH3O3SCs, 6 mM CsCl (intracellular Cs was used to block potassium channels), 2 mM Mg Cl2, 10 mM HEPES, 1.1 EGTA, 5 mM Lidocaine N-ethyl bromide (QX-314, to block sodium channels), 4 mM ATP-Mg, pH 7.3 (adjusted with 1 M CsOH) and 290–300 mOsm/L. Neurons were voltage-clamped at −20 mV. GABA synaptic responses were recorded using an Axopatch 1D amplifier (Axon Instruments, Union City, CA, USA), digitized using a Digidata 1200 interface (Axon Instruments) and stored on a computer. On-line analysis and storage of current data into data files performed using the pClamp 6.0.4 software from Axon Instruments. In all experiments, stimuli (0.2 msec duration, 0.3–1 mA intensity, 0.25 Hz) were applied to determine the postsynaptic response amplitudes and to measure the time-dependent effects of drugs. Drugs were diluted in the external medium to the desired concentration and applied by bath perfusion (ghrelin: 300 nM, hOb/hObQ90L: 10, 30, 100 and 300 nM). After acquisition of a 10 minutes baseline of current amplitudes, hOb and hObQ90L were applied for 5–6 minutes, followed by 10 minutes washing periods. Amplitudes of induced synaptic currents were normalized relative to the baseline prior to the application of drugs.
Values are given as mean±SEM, and statistical analysis were performed using ANOVA, repeated measure ANOVA followed by a Fisher post-hoc test when the p value of the ANOVA was significant (P<0.05) using statview software (SAS institute Inc., Cary, NC, USA).
Areas Under the Curve (AUC) were calculated by the trapezoidal method.
The effects of the drugs in electrophysiological experiments were determined by comparing the best-fit values of two dose-response curves using Student T-test in the GraphPad PRISM 5 software (GraphPad Software, San Diego, CA, USA). The effect were different if P<0.05.
(A) Mean cumulative 4 h food intake after the different treatments in low responders. (B–D) Meal number, size and duration within 4 h following treatment in low responders. Data represent mean±SEM. *P<0.05 vs saline, **P<0.01 vs saline, #P<0.05 vs ghr.
(A) Mean GH secretion in response to the different treatments in low responders. (B) Area Under the curve of GH secretion over 4 h in low responders. Data represent mean±SEM.
Effect of native (h/rOb) and Q90L obestatin (hObQ90L) on ghrelin-induced (Ghr) cFos immunoreactivity in ARC NPY and GHRH neurons in C57BL/6 mice.
We are grateful to Dr ICAF Robinson (National Institute for Medical Research, Mill Hill, London, England) for providing the GHRH-EGFP mice and to Dr Parlow (NHPP, Los Angeles, USA) for the GH reagents. We are thankful to Alice Cougnon for animal care.
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