Central Administration of Leptin to Ovariectomized Ewes Inhibits Food ...

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BELINDA A. HENRY, JAMES W. GODING, WARREN S. ALEXANDER,. ALAN J. ... Victoria 3181; the Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital. (W.S.A.) ... and in some cases this is associated with a failure to undergo ... Address all correspondence and requests for reprints to: Dr. Iain J.
0013-7227/99/$03.00/0 Endocrinology Copyright © 1999 by The Endocrine Society

Vol. 140, No. 3 Printed in U.S.A.

Central Administration of Leptin to Ovariectomized Ewes Inhibits Food Intake without Affecting the Secretion of Hormones from the Pituitary Gland: Evidence for a Dissociation of Effects on Appetite and Neuroendocrine Function* BELINDA A. HENRY, JAMES W. GODING, WARREN S. ALEXANDER, ALAN J. TILBROOK, BENEDICT J. CANNY, FRANK DUNSHEA, ALEXANDRA RAO, ASHLEY MANSELL, AND IAIN J. CLARKE Prince Henry’s Institute of Medical Research (B.A.H., A.R., I.J.C.), Clayton, Victoria 3168; the Department of Immunology and Pathology, Monash University Medical School (J.W.G.), Prahran, Victoria 3181; the Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital (W.S.A.), Parkville, Victoria 3050; the Department of Physiology, Monash University (A.J.T., B.J.C.), Clayton, Victoria 3168; Victorian Institute of Animal Science (F.D.), Werribee, Victoria 3030; and Swinburne University of Technology (A.M.), Hawthorn, Victoria 3122, Australia ABSTRACT We have studied the effect of leptin on food intake and neuroendocrine function in ovariectomized ewes. Groups (n 5 5) received intracerebroventricular infusions of either vehicle or leptin (20 mg/h) for 3 days and were blood sampled over 6 h on days 21, 2, and for 3 h on day 3 relative to the onset of the infusion. The animals were then killed to measure hypothalamic neuropeptide Y expression by in situ hybridization. Plasma samples were assayed for metabolic parameters and pituitary hormones. Food intake was reduced by leptin, but did not change in controls. Leptin treatment elevated plasma lactate and nonesterified fatty acids, but did not affect glucose or insulin levels, indicating a state of negative energy balance that was met by

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EPTIN is a hormone produced by adipocytes that may signal the brain as a satiety factor (1, 2). Mutations in the leptin gene (3) or in the receptor (4) can lead to obesity, and in some cases this is associated with a failure to undergo puberty. In addition, a number of studies in rodents have shown that leptin can affect endocrine function, especially the secretion of hormones from the anterior pituitary (5– 8), ovary (9, 10), and adrenal (11). Leptin treatment stimulates the secretion of gonadotropins in ob/ob mice (12), reverses the delay in puberty caused by dietary restriction in female rats (13), and may advance puberty in normal mice (14, 15). Intraperitoneal injection of leptin prevents the fall in plasma concentrations of thyroid hormones and gonadotropins that occurs during fasting in mice and also blunts the fastinginduced elevation in plasma ACTH levels (5). Intracerebroventricular (icv) injection of leptin corrected the reduction in Received July 9, 1998. Address all correspondence and requests for reprints to: Dr. Iain J. Clarke, Prince Henry’s Institute of Medical Research, P.O. Box 5152, Clayton, Victoria 3168, Australia. E-mail: [email protected]. * This work was supported by the National Health and Medical Research Council of Australia, The Buckland Foundation, and the Victoria Health Promotion Foundation.

the mobilization of body stores. Pulse analysis showed that the secretion of LH and GH was not affected by leptin treatment, nor were the mean plasma concentrations of FSH, PRL, or cortisol. Expression of messenger RNA for neuropeptide Y in the arcuate nucleus was reduced by the infusion of leptin, primarily due to reduced expression per cell rather than a reduction in the number of cells observed. Thus, the action of leptin to inhibit food intake is dissociated from neuroendocrine function. These results suggest that the metabolic effects of leptin are mediated via neuronal systems that possess leptin receptors rather than via endocrine effects. (Endocrinology 140: 1175– 1182, 1999)

GH in fasted mice (7) and increased GH secretion in pigs (8). It is presumed that any central effect of leptin on the endocrine system would be mediated via the hypophysiotropic hormones, which would, in turn, affect the secretion of the relevant hormones from the anterior pituitary gland. Although this has not been shown in vivo, there is in vitro evidence for leptin regulation of GnRH (6) and somatostatin (16) secretion. There is also in vitro evidence for the action of leptin in the rat pituitary gland to regulate the secretion of LH, FSH, and PRL (6). One question that is central to the issue of how leptin may affect endocrine function is whether there is a direct effect on neuroendocrine cells in the hypothalamus or whether there is an indirect effect via neuronal systems that possess the leptin receptor. For example, neuropeptide Y (NPY) cells express the leptin receptor and could act to regulate appetite (2, 17) and neuroendocrine function (18 –20). Thus, centrally administered leptin could act on appetite regulatory systems within the hypothalamus, which could, in turn, influence the function of neuroendocrine cells. There are various precedents for this, one being that melanin-concentrating hormone regulates appetite (21), but also appears to regulate the secretion of GnRH (22) and CRF (18, 23). Another possibility

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is that leptin could directly affect neuroendocrine cells. Zamorano et al. (24) used RT-PCR to demonstrate the existence of the leptin receptor in GT1–7 cells. Others (Moenter, S., personal communication), however, found that leptin cannot affect the secretion of GnRH from GT cells unless the immortalized neurons are transfected with the receptor. We investigated the effect of centrally administered leptin on the secretion of pituitary hormones in the sheep. It was hypothesized that a dose of leptin that acted to inhibit food intake would be capable of influencing endocrine function. Materials and Methods

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gradient of 0.1% trifluoroacetic acid in water to 70% acetonitrile-0.1% trifluoroacetic acid, followed by lyophilization. A single major peak that eluted late in the gradient was the only species that had biological activity, as assessed by induction of proliferation in the factor-dependent cell line BAF-3 that had been transfected with the human leptin receptor (25). Biological activity per unit mass was comparable to that purified by nondenaturing affinity chromatography from supernatant of the same gene expressed in COS cells, compatible with the idea that refolding was essentially complete. The recombinant leptin had a molecular mass of 16,000 daltons, as determined by SDS-PAGE. Figure 1 shows the bioactivity of this material assessed in the in vitro cell proliferation bioassay. The material was stored in 0.1 m HCl at 4 C before infusion and infused in the same vehicle at a concentration of 0.18 mg/ml. A high dose of leptin was used to ensure a significant reduction in food intake; this was based on the results of preliminary studies.

Ethics This work was approved in advance by the Animal Experimentation Ethics Committees of Monash University and Victoria Institute of Animal Science.

Animals, surgery, infusions, and blood sampling Corriedale ewes with a mean body weight of 44.6 6 1.2 kg were used during the breeding season. The animals were ovariectomized at least 1 month before surgery and were fitted with guide tubes into the third cerebral ventricle (3V) as previously described by Barker-Gibb et al. (19). The animals were tamed and familiarized with the experimental facilities and were housed in individual pens for the duration of the experiment. On the day before commencement of infusions and blood sampling, one external jugular vein was cannulated, and the cannula was kept patent with heparinized (50 U/ml) normal saline. The animals were fed 1.5 kg Lucerne chaff/day, and refusals were weighed to monitor food intake from 5 days before the start of the infusion until the end of the experiment. For the infusion of leptin or vehicle, we used Graseby MS16A infusion pumps (Graseby Medical Ltd., Gold Coast, Australia) strapped onto the backs of the animals. Polyethylene tubing was connected to a 2.5-ml plastic syringe and to a 19-gauge stainless steel tubing assembly that was introduced into the 3V at least 2 mm beyond the end of the guide tube. The patency of the system was verified by checking that cerebrospinal fluid flowed out of the infusion cannulas. Groups of five sheep were randomly assigned to two groups to receive either vehicle or leptin, infused into the 3V at a rate of 110 ml/h (20 mg/h). The infusion syringes were filled once a day, using a side port in the infusion line. Blood samples (8 ml) were taken from the jugular venous cannulas that were extended with a manometer line (Portex Ltd., Kent, UK) and closed with a three-way tap. Samples were collected into heparinized tubes and centrifuged at 4 C to obtain plasma, which was stored at 220 C until assayed. The animals were sampled at 10-min intervals for 6 h (commencing at 0900 h) on days 21 and 2 relative to the start of the infusion and again on day 3 for 3 h. After this, the animals were injected (iv) with an overdose of pentobarbitone (Lethabarb, May and Baker Pty. Ltd., Australia) and decapitated. The hypothalamus was dissected, frozen on dry ice (within 2 min of decapitation), and stored at 280 C for in situ hybridization.

RIAs LH. Plasma samples (100 ml) were assayed in duplicate by the method of Lee et al. (26), using the ovine standard NIH oLH-S18. In nine assays the sensitivity was 0.1 ng/ml; the intraassay coefficient of variation (CV) was less than 10% over the range 0.88 –18.1 ng/ml, and the interassay CV was 17%. FSH. Every tenth sample was assayed (100 ml) in duplicate using the method of Bremner et al. (27) with the ovine standard NIAMMD oFSHRP-1. The sensitivity of two assays was 1.3 ng/ml; the intraassay CV was less than 10% between 0.95–21.8 ng/ml, and the interassay CV was 6.1%. PRL. Samples were assayed in duplicate at a volume of 10 ml following the method of Clarke et al. (28) and with the ovine standard Sigma Chemical Co. (lot 114F-0558, St. Louis, MO). The sensitivity of nine assays was 0.15 ng/ml; the intraassay CV was , 10% over the range 1.5– 6.8 ng/ml, and the interassay CV was 20%. GH. Samples were assayed in duplicate at a volume of 200 ml using the method of Thomas et al. (29) with NIDDK oGH-I-4 as the standard. The

Recombinant human leptin Leptin complementary DNA was isolated from human adipose tissue by the PCR and cloned into the bacterial expression vector pCAL-n (Stratagene, La Jolla, CA), and its authenticity was verified by DNA sequencing. Recombinant leptin was produced by transformation of BL-21(LysS) Escherichia coli, followed by growth in trypton-phosphate broth and induction with isopropyl b-d-galactoside. Bacteria were lysed by freezing and thawing followed by sonication, and DNA was digested with deoxyribonuclease I. Inclusion bodies were washed twice in 10 mm Tris-HCl, pH 8, containing 0.1% Triton X-100, followed by one wash in the same buffer lacking detergent. Inclusion bodies were then solubilized in 9 m urea and 5 mm dithiothreitol at room temperature, and the insoluble material was removed by centrifugation. Leptin was refolded by slow dropwise dilution into 10 vol 10 mm HCl with rapid stirring and was finally purified by reverse phase HPLC using C4-silica and a linear

FIG. 1. Proliferation of the dependent cell line BAF-3 that had been transfected with the human leptin receptor, indicating the activity of a human leptin standard (upper panel) and the recombinant material that was prepared for this study (lower panel).

LEPTIN AND NEUROENDOCRINE FUNCTION IN SHEEP sensitivity of 8 assays was 0.5 ng/ml; the intraassay CV was less than 10% over the range of 1.9 –27.1 ng/ml, and the interassay CV was 20%. Cortisol. All samples were assayed in duplicate at 100 ml, using the RIA outlined by Bocking et al. (30). One hundred microliters from every sample were placed into a daily pool for each individual sheep. These pools were used for cortisol, glucose, lactate, nonesterified fatty acid, and insulin. For four cortisol assays, the sensitivity was 0.2 ng/ml; the intraassay CV was 9.9%, and the interassay CV was 13.3% at 20.7 ng/ml and 10% at 14.8 ng/ml. Insulin. Samples were assayed using a kit (Linco Research, Inc., St. Charles, MO) with human insulin as a standard and validated for ovine insulin in our laboratory. All analyses were performed in a single assay, and the intraassay CV was 2.5%. Nonesterified fatty acids (NEFA). Plasma NEFA were analyzed using an enzymatic kit assay (31). All analyses were performed in a single assay, and the intraassay CV was 4.1%. Glucose and lactate. Blood glucose and lactate concentrations were measured in 25-ml samples of plasma using a YSI2300 STAT glucose/llactate analyzer (Yellow Springs Instrument Co., Yellow Springs, OH). The measurable range for blood glucose was between 0 –30 mm and was 0 –16 mm for lactate.

In situ hybridization Hypothalamic sections (16 mm) were cut on a freezing microtome and were thaw-mounted onto warm slides. In situ hybridization was performed using a 35S-labeled 48-mer oligonucleotide sequence complementary to 159 –206 of the coding region of human NPY, as previously described (32). Hybridization was carried out at 42 C in a humid chamber; after posthybridization treatment, sections were taped to an x-ray cassette. Slides were exposed to Kodak X-omatic AR film (Kodak, Australasia, Coburg, Australia) for 12 days at room temperature before being developed. Carbon14 standards (Americal Radiolabeled Chemicals, Inc., St. Louis, MO) were used to calibrate the index of labeling and therefore quantify the total amount of hybridization. The smallest two standards were plotted against a known index of staining (disintegrations per min/mm2), and the background was defined as zero, providing a standard curve for the quantification of labeling density. Slides were then dipped in Ilford K5 photographic emulsion (Ilford Australia, Mount Waverly, Australia), exposed at 4 C for 7 nights, and developed using Ilford phenisol x-ray developer, stop bath, and Hypam fixer. Sections were counterstained with 1% cresyl violet and coverslipped using DPX (BDH Laboratory Supplies, Melbourne, Australia). Analysis at the cellular level was carried out on the emulsion-dipped slides. Five labeled cells per section were analyzed by counting silver grains under 3400 magnification, and the number of cells expressing NPY messenger RNA (mRNA) was counted at 320 magnification. Densitometry and silver grain counts were performed using the microcomputer imaging device M1 system from the Imaging Research, Inc. (Brock University, St. Catherines, Canada).

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values. Nontransformed data are presented as the mean 6 sem. Repeated measures ANOVA was used to analyze the in vivo data, and paired comparisons were made between groups on each day of the experiment. Least significant differences were used to test for significant differences between means. Data on the expression of NPY mRNA in the arcuate nucleus were analyzed by single factor ANOVA. Data for the number of silver grains per cell were subjected to square root transformation.

Results Food intake (Fig. 2)

Food intake was similar in the control and leptin-treated animals throughout the preinfusion period. Leptin treatment significantly decreased (P , 0.05) food consumption within 24 h, and intake was lower in the leptin-treated group at 48 and 72 h compared with that in control animals. Plasma levels of pituitary hormones and cortisol (Figs. 3 and 4)

Leptin infusion did not significantly affect mean plasma concentrations of either LH or GH and did not affect interpulse interval or pulse amplitude for either of these hormones. The mean plasma concentrations of FSH, PRL, and cortisol were not affected by the infusion of leptin. Metabolic indicators (Fig. 5)

Plasma glucose and insulin concentrations were not significantly altered during the leptin infusion, but plasma lactate concentrations were significantly (P , 0.05) increased after 72 h of leptin treatment. The concentrations of NEFA were significantly (P , 0.01) increased at both 48 and 72 h relative to preinfusion levels, and NEFA concentrations were significantly (P , 0.01) higher in the leptin-treated animals compared with those in the control group at these time points. In situ hybridization for hypothalamic NPY

The total hybridization signal for NPY in the arcuate nucleus of the leptin-treated animals was significantly (P ,

Data analysis Pulse analysis was performed for patterns of LH and GH secretion, and mean daily levels were used to study effects on the other hormones and metabolic parameters. LH pulses were defined as previously described (33). The mean GH concentration, interpulse interval, and pulse amplitude were determined using the TURBOPULSAR program (34). This program enables the selection of both high narrow peaks and smaller broad peaks based on the G parameters. The G parameters used were G(1) 5 4.4, G(2) 5 2.0, G(3) 5 1.0, G(4) 5 0.75, and G(5) 5 0.5. The within-assay CV and assay sensitivity were also taken into consideration, as defined by Fletcher and Clarke (34) in the following quadratic equation: y 5 24.4 (log x)2 2 42.7 log x 1 24.1.

Statistical analysis All data were checked for homogeneity of variance; the average plasma concentrations were subjected to square root transformation, and the data for plasma glucose and lactate were transformed to log

FIG. 2. The effect of icv infusion of vehicle or leptin on the mean (6SEM) daily food intake. *, P , 0.05 compared with pretreatment.

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FIG. 3. The effect of icv infusion of leptin on the mean (6SEM) plasma concentrations of LH and GH and the interpulse intervals and pulse amplitude for these hormones. Open columns represent control (vehicle infusion) data, and shaded columns represent data from leptin-infused animals.

Discussion

FIG. 4. The effect of icv infusion of leptin on the mean (6SEM) plasma concentration of FSH, PRL, and cortisol. Open columns represent control (vehicle infusion) data, and shaded columns represent data from leptin-infused animals.

0.05) lower than that in the vehicle-infused animals (6.45 6 0.55 vs. 9.14 6 0.16 dpm/mm2; Figs. 6 and 7). There was no significant difference in the number of cells labeled for NPY mRNA in the arcuate nucleus between the two groups, but a significant (P , 0.01) decrease was observed in the number of silver grains per cell in the leptin-treated animals (Figs. 6 and 7).

These data show that the appetite-regulating effect of leptin may not necessarily be associated with alterations in neuroendocrine function in the sheep. At the dose used, leptin clearly inhibited food intake, but did not affect any of the endocrine parameters examined. This contrasts with earlier studies in monogastric species and may be a reflection of the efficient gluconeogenic system in the ruminant and the ability to adapt to a number of days of moderate undernutrition. It is now clear that leptin is a satiety factor in a wide range of species, including rodents (1, 2) and pigs (8). In addition, a range of studies in the rodent (5, 7, 8, 12, 35) and pig (8) has shown that leptin may regulate neuroendocrine function. The hypophysiotropic peptides of the hypothalamus regulate pituitary hormone secretion, and it is most likely that the effects of centrally administered leptin on endocrine function would involve some alteration in the secretion of these peptides. In rodents, either centrally (7) or peripherally (5, 12, 36) administered leptin will alter endocrine function. Whether this is due to direct action on the hypophysiotropic cells of the hypothalamus or on the endocrine cells of the pituitary gland is not yet clear. Leptin receptors have been identified in the hypothalamus (17, 24, 37, 38), but there has as yet been no report of these receptors on neuroendocrine cells. Likewise, receptors have been demonstrated at the level of the pituitary gland, but the cell types on which they are found have not been defined. As the hypothalamic receptors can be localized to neurons that contain neuropeptide Y (17) and POMC (39), it would seem most likely that any effects on neuroendocrine function would be relayed through such cells. These neuropeptides affect both endocrine function (20) and appetite (40); it might be supposed that leptin would alter both. This is not necessarily the case in the sheep and raises doubts about extrapolating the data that have been obtained in rodents to nonrodent species. It should be noted, however, that the types of cells that express leptin receptor

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FIG. 5. The effect of icv infusion of leptin on the catabolic state of the animals indicated by mean (6SEM) plasma concentrations of glucose, insulin, lactate, and NEFA. Open columns represent control (vehicle infusion) data, and shaded columns represent data from leptin-infused animals. *, P , 0.05; **, P , 0.01 (compared with the preinfusion).

FIG. 6. Examples of in situ hybridization with a NPY oligonucleotide probe on arcuate nucleus sections from ovariectomized ewes given icv infusions of either vehicle (a) or leptin (b) (counterstained with cresyl violet; magnification, 340).

in the ovine brain remains unknown, and species differences may well exist in this regard. Bronson (41) has indicated that alterations in food intake in rodents have a profound impact on reproductive function in a short time frame (,1 day), because these animals do not generally have large fat reserves. This contrasts with other species in which fat reserves are considerable. For example, the ideal body fat composition of the human female is 22% (42). Likewise, it has been shown that peripheral (5) and central (7) administration of leptin to starved mice/rats has a profound short term effect on the secretion of pituitary hormones. There have, however, been only limited studies carried out on other species. In pigs, an icv injection of 10 mg (and higher doses) leptin increased the secretion of GH. Our present data, in contrast, show no effect on GH levels during a 3-day infusion of a appetite-reducing dose of leptin. The ruminant animal is capable of maintaining glycemia

during periods of moderate negative energy balance (43). In the present study, icv leptin infusion and the associated reduction in food intake moved the sheep into negative energy balance, as indicated by plasma metabolites. For example, the increase in plasma NEFA concentrations that we observed is a clear indication of the mobilization of considerable amounts of fat reserves to spare glucose utilization (44, 45). During a period of extended undernutrition, plasma lactate normally decreases as glycogen stores are depleted (46), but over a period of semiacute undernutrition, as in the present study, plasma lactate concentrations would increase with mobilization of muscle glycogen and an increase in glucose carbon recycling. Accordingly, the sheep in the present study were able to maintain blood glucose levels by using mobilized NEFA as an alternative energy source and increasing gluconeogenesis from mobilized lactate, glycerol, and amino acids. It has been shown previously that restricted

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FIG. 7. Effect of icv infusion of leptin on expression of NPY in the arcuate nucleus of ovariectomized ewes (n 5 5). The mean (6SEM) total index of labeling measured directly from x-ray film (see Materials and Methods for details; upper panel), number of cells (middle panel), and silver grains per cell (lower panel). *, P , 0.05; **, P , 0.01.

food intake does not alter plasma insulin levels in the sheep (43), and the present results are in accord with these earlier findings. The situation is somewhat different from that obtained with food deprivation over 1–2 days in the primate (47), in which plasma glucose and insulin levels fall. Insulin levels probably play a significant role in the production of leptin in nonruminant species (48). Thus, to put the present results in context, we emphasize that the ruminant is a special case. Using the sheep, we have demonstrated the ability of leptin to reduce food intake over a period of 3 days without an effect on the secretion of pituitary hormones. This strongly suggests that when blood glucose and insulin levels are maintained, leptin does not have a direct effect on the neuroendocrine system. The animals of this study were ovariectomized, and this may have a significant bearing on the results, especially with respect to gonadotropin secretion. The secretion of GnRH is not restrained by gonadal hormone feedback in the ovariectomized animal, and the ability of leptin to increase the secretion of GnRH or the gonadotropins (the former was not measured in this study) might be minimal. Yu et al. (6) reported small effects of leptin on the secretion of GnRH from hypothalamic fragments in vitro, but there are, as yet, no studies on the effects of leptin on GnRH secretion in vivo. Although it has been reported that immortalized GnRH neurons contain leptin receptors (24), these cells do not respond to leptin with an increase in GnRH secretion (Moenter, S.,

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personal communication). To warrant the measurement of GnRH secretion in vivo, an effect on gonadotropin secretion would first have to be demonstrated. It is possible that leptin acts directly on the pituitary gland to influence the secretion of the gonadotropins, PRL, and other pituitary hormones, but iv infusion of the same amount of leptin (20 mg) over the same time course (3 days) had no effect (Clarke, I. J., unpublished data). A recent publication (49) showed that leptin prevents the reduction in pulsatile LH secretion that is seen in fasted female rats that received either vehicle or estrogen. As leptin treatment restored the frequency of LH pulses, this suggested action at the central level to influence GnRH secretion. Leptin did not overcome the negative feedback effect of estrogen. It remains possible that an interaction exists between leptin and steroid effects on GnRH secretion in the sheep, and current studies are investigating this. We (21) have previously shown that low dietary intake, which decreased body weight in ewes, elevated plasma GH levels, whereas overweight sheep have reduced GH levels (29, 33). If leptin is to be regarded as the metabolic indicator that signals the amount of fat stores, then it might be expected to reduce plasma GH levels in sheep. It was somewhat surprising, therefore, that leptin did not alter the plasma levels of GH in the present study. Carro et al. (7) showed that leptin could restore plasma levels of GH to normal if administered to starved rats, in which GH secretion is reduced, but an effect was not seen in normally fed animals. Recent in vitro studies (50) have shown that leptin reduces the responsiveness of ovine pituitary somatotropes to GH-releasing hormone, but stimulates GH secretion. In pigs, icv injection of 10 mg leptin (and higher doses) (8) reduced food intake and increased plasma GH levels. Whether this reflects a difference between monogastric species and ruminants is not clear at this stage. It would seem likely that these doses in rodents are probably supraphysiological. Continuous infusion of smaller doses, rather than large bolus doses, of leptin may be expected to have different effects. As mentioned above, a single icv injection of leptin caused an increase in GH secretion in pigs (8). This is not consistent with the idea that leptin signals an increase in adiposity that is associated with reduced plasma GH levels in most species. On the other hand, it is consistent with the well documented effect of fasting, which increases plasma GH levels (51). Thus, it might be the case that the effect of leptin in the pig is an indirect effect of reduced food intake rather than a direct action of the satiety factor. It should also be noted that these results were obtained with a single injection of leptin. We have been unable to show an effect of a 24-h infusion of 8.3 mg/h leptin on food intake or hormone levels in sheep (Henry, B., and I. J. Clarke, unpublished data). This suggests that a longer infusion time might be required to obtain any meaningful effect in this species. It was not possible to do this in the current study with the dose that we used, because food intake was severely reduced in some animals, and continuation would not have been ethically acceptable. Using lower doses of leptin would enable a longer period of treatment and could yield different results. In addition to the effects on the reproductive axis and GH levels in rodents, leptin has been shown to influence the function of the hypothalamo-pituitary-adrenal (5, 36) and the

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hypothalamo-pituitary-thyroid (5, 35) axis. The importance of leptin in maintaining endocrine function is evident in ob/ob mice, which suffer a number of anomalies, including diabetes, hypercorticoidism, and hypothyroidism (52). Consistent with the lack of an effect of icv leptin infusion on plasma gonadotropin and GH levels, we have also shown that this treatment does not affect plasma PRL and cortisol levels. The latter gives some representation of the hypothalamo-pituitary-adrenal axis. Thus, we conclude that satiety-inducing doses of leptin do not affect the neuroendocrine systems, although we have not studied the hypothalamo-pituitarythyroid axis. Leptin treatment decreased the expression of NPY mRNA in the arcuate nucleus, which is consistent with previous studies in the rodent species (5, 53). The decrease was due to a reduction in the expression of NPY and not to a decrease in the number of NPY-labeled cells. The leptin receptor is expressed in NPY-containing cells in the rodent (17), and this neuropeptide plays a central role in the control of appetite. The obesity syndrome in ob/ob mice is attenuated in NPY gene knockout mouse. Double mutant mice (ob/ob NPY2/2) are less obese, have lowered food intake and increased energy expenditure, and do not show the same incidence of diabetes, sterility, and somatotropic defects that is seen in ob/ob (54). In the sheep, there is evidence that NPY regulates the GnRH-LH axis (19) and CRF-arginine vasopressin secretion (18). In the present study, however, we observed a decrease in the expression of NPY, but this was without effect on the secretion of pituitary hormones or cortisol. One possible explanation could be that leptin acts on a subset of NPY cells that regulates appetite, but not on those NPY cells that regulate hypophysiotropic neurons. Other cells (e.g. POMC) in the arcuate nucleus (39, 55, 56) or in other parts of the brain (57, 58) may also mediate the effect of leptin. In conclusion, we have shown that leptin can inhibit food intake in sheep, but, in contrast to the results obtained in other species, the satiety-inducing dose of leptin was unable to alter plasma levels of LH, FSH, GH, PRL, and cortisol. A catabolic state was achieved with leptin treatment, but this did not alter the plasma glucose concentration. These results suggest that the metabolic factors that regulate food intake may be different from those that regulate neuroendocrine function. Acknowledgments We thank Mr. Bruce Doughton and Ms. Karen Perkins for animal care. Hormone reagents and standards were supplied by the National Hormone and Pituitary Program of the NIDDK.

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