The effects of kisspeptin on food intake in women with overweight or obesity

Kisspeptin is recognized to have a critical role in the control of reproductive function; however, as reproductive processes require adequate energy stores, there is increasing focus on its interaction with metabolic processes. Female (but not male) kisspeptin receptor knockout mice exhibit reduced food intake, consistent with an orexigenic action of kisspeptin. Furthermore, some of these effects persist even after global female kisspeptin receptor knockout mice are rendered eugonadal via selective re-expression of the kisspeptin receptor in gonadotrophin-releasing hormone neurons. Conversely, in vitro studies show that kisspeptin stimulates anorexigenic pro-opiomelanocortin neurons and inhibits orexigenic neuropeptide Y neurons, indicating that kisspeptin may have anorexigenic effects. Similarly, kisspeptin administration studies in animals have yielded conflicting results. Acute central administration of kisspeptin reduces food intake in male rodents. Acute peripheral kisspeptin administration reduces food intake in both male and female mice. However, chronic central or peripheral kisspeptin administration does not influence food intake in male rats. To date, there are only limited data investigating the effect of kisspeptin on food intake in humans. In young men with normal bodyweight, acute intravenous kisspeptin administration does not affect appetite and food intake. However, there are no studies investigating the effect of kisspeptin on food intake in women, nor in people with overweight or obesity. Therefore, we undertook this study to determine the effect of kisspeptin on appetite and food intake in women with overweight or obesity and test our hypothesis that kisspeptin would have an orexigenic effect in women with overweight or obesity.


| BACKGROUND
Kisspeptin is recognized to have a critical role in the control of reproductive function 1,2 ; however, as reproductive processes require adequate energy stores, there is increasing focus on its interaction with metabolic processes. Female (but not male) kisspeptin receptor knockout mice exhibit reduced food intake, 3,4 consistent with an orexigenic action of kisspeptin. Furthermore, some of these effects persist even after global female kisspeptin receptor knockout mice are rendered eugonadal via selective re-expression of the kisspeptin receptor in gonadotrophin-releasing hormone neurons. 4 Conversely, in vitro studies show that kisspeptin stimulates anorexigenic pro-opiomelanocortin neurons and inhibits orexigenic neuropeptide Y neurons, 5 indicating that kisspeptin may have anorexigenic effects.
Similarly, kisspeptin administration studies in animals have yielded conflicting results. Acute central administration of kisspeptin reduces food intake in male rodents. 6,7 Acute peripheral kisspeptin administration reduces food intake in both male and female mice. 8 However, chronic central or peripheral kisspeptin administration does not influence food intake in male rats. 9 To date, there are only limited data investigating the effect of kisspeptin on food intake in humans. In young men with normal bodyweight, acute intravenous kisspeptin administration does not affect appetite and food intake. 10 However, there are no studies investigating the effect of kisspeptin on food intake in women, nor in people with overweight or obesity. Therefore, we undertook this study to determine the effect of kisspeptin on appetite and food intake in women with overweight or obesity and test our hypothesis that kisspeptin would have an orexigenic effect in women with overweight or obesity.

| METHODS
This single-blinded crossover study was approved by the West London Research Ethics Committee (16/LO/0391) and registered on the ISRCTN Trial Registry (ISRCTN10114288). Written informed consent was given by all participants. Women aged 18-60 years with a body mass index >25 kg/m 2 were recruited via advertisements. Exclusion criteria included pregnancy, breastfeeding, psychological conditions, use of recreational or investigational drugs within the preceding 2 months, use of drugs that are known to affect appetite within the preceding 2 months, use of oral and/or transdermal oestrogen or progestin within the preceding 3 months, blood donation within 3 months of study participation, ingestion or inhalation of nicotine-containing substances, alcoholism and malignancy.
Following a taste test to select the study meal based on Likert scores closest to 'neither like nor dislike', each participant attended two study visits. Each study visit was identical apart from the infusion.
During one study visit, an intravenous infusion of kisspeptin-54 at 1.0 nmol/kg/h was administered (i.e. a dose known to produce reproductive and metabolic effects in humans 10 ), and rate-matched vehicle was administered during the other study visit, with the order of infusions randomly determined using random.org. For each premenopausal woman, both study visits were conducted during the same phase of the menstrual cycle. In the 24-h period preceding each study visit, participants were asked to refrain from strenuous exercise, alcohol and caffeine. Each participant ate their evening meal at 8 pm on the night preceding each study visit and thus attended each study visit after an overnight 14-h fast. Following a period of acclimatization, blood samples were taken regularly via an intravenous cannula Laboratory of Imperial College Healthcare NHS Trust. Chemiluminescent immunoassays were used to measure serum insulin (intra-assay and inter-assay CV: ≤7%), serum LH (intra-assay and inter-assay CV: ≤5%) and serum oestradiol (intra-assay and inter-assay CV: ≤8%).
Based on our previous work, in which acute intravenous hormone infusion reduced food intake in healthy men, 11 a sample size of 16 people would have 90% power (at a significance level of 0.05) to detect a clinically significant reduction in food intake of 2.3 ± 1.3 kcal/kg. For a woman with a weight of 100 kg, 2.3 kcal/kg would equate to 230 kcal/meal, and thus 690 kcal/day assuming three meals are eaten per day (which is equivalent to one-third of the 2000 kcal/day recommended intake for women 12 ). Statistical analysis was performed using Prism 9.4.1 (GraphPad) and data are presented as mean ± SEM. Paired t-tests were performed on parametric data, and Wilcoxon matched-pairs signed rank tests were performed on non-parametric data. Two-way ANOVAs or mixed effects models (if there were incomplete data at some timepoints) were performed on visual analogue scales, LH, oestradiol, glucose and insulin curves. Statistical significance was set at p < .05.

| CONCLUSIONS
In this study, we showed that a biologically active dose of kisspeptin did not affect self-reported appetite and did not affect objectively measured food intake in women with overweight or obesity. In addition, intravenous administration of kisspeptin did not influence preprandial and postprandial glucose and insulin levels in women with overweight or obesity. This is the first study to report on the effect of kisspeptin on appetite, food intake, glucose and insulin levels in women, and in people who are overweight or have obesity. These results are consistent with a study of kisspeptin administration in men with normal bodyweight. 10 Furthermore, as previously reported in men, 10 kisspeptin did not enhance glucose-stimulated insulin secretion when glucose levels remained within physiological limits in women. Kisspeptin administration robustly increased LH levels, in keeping with its known reproductive effects in women with normal weight. 2 Oestradiol is known to influence appetite, 13 but oestradiol levels remained unchanged before consumption of the meal.
Because of the contradictory preclinical literature, [6][7][8][9] it is necessary to conduct studies in humans to determine if there are species-specific effects. Furthermore, as sexually dimorphic effects on food intake in kisspeptin receptor knockout rodents have been reported, 3 this study enhances our knowledge of the metabolic effects of kisspeptin in humans across genders. As the therapeutic potential of kisspeptin for use in metabolic disorders is being investigated, 14 this study provides reassurance that kisspeptin-based treatments are unlikely to be directly orexigenic in women and in people with overweight or obesity.
The strengths of this study include the crossover design, which