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1.
Public Health Nutr ; 27(1): e107, 2024 Mar 20.
Article in English | MEDLINE | ID: mdl-38504524

ABSTRACT

OBJECTIVES: Individuals often use self-directed strategies to manage intake of tempting foods, but what these strategies are and whether they are effective is not well understood. This study assessed the frequency of use and subjective effectiveness of self-directed strategies in relation to BMI and snack intake. DESIGN: A cross-sectional and prospective study with three time points (T1: baseline, T2: 3 months and T3: 3 years). At T1, demographics, frequency of use and subjective effectiveness of forty-one identified strategies were assessed. At T2 and T3, current weight was reported, and at T2 frequency of snack intake was also recorded. SETTING: Online study in the UK. PARTICIPANTS: Data from 368 participants (Mage = 34·41 years; MBMI = 25·06 kg/m2) were used for analysis at T1, n = 170 (46·20 % of the total sample) at T2 and n = 51 (13·59 %) at T3. RESULTS: Two strategy factors were identified via principal axis factoring: (1) diet, exercise, reduction of temptations, and cognitive strategies, and (2) planning, preparation and eating style. For strategy 1, frequency of use, but not subjective effectiveness, was positively related to BMI at T1. Subjective effectiveness predicted an increase in BMI from T1 and T2 to T3. No relationship to snack intake was found. For strategy 2, frequency of use was negatively related to BMI at T1. Neither frequency of use nor subjective effectiveness were related to changes in BMI over time, but subjective effectiveness was negatively correlated with unhealthy snack intake. CONCLUSION: Self-directed strategies to reduce the intake of tempting foods are not consistently related to BMI or snack intake.


Subject(s)
Diet , Snacks , Humans , Adult , Body Mass Index , Cross-Sectional Studies , Prospective Studies , Energy Intake , Feeding Behavior/psychology
2.
Br J Nutr ; 130(7): 1267-1277, 2023 10 14.
Article in English | MEDLINE | ID: mdl-36645103

ABSTRACT

'Dietary variety' has been identified as a factor associated with food intake. Whilst this relationship may have longer-term benefits for body weight management when eating low-energy, nutrient-dense foods, it may increase the risk of overconsumption (and body adiposity) when foods are high energy density. This study sought to further explore pathways underpinning the relationship between dietary variety and body weight, by considering energy density as a moderating factor and portion size as a mediating factor in this relationship. Using prospective data from the UK Biobank, dietary variety scores (DVS), cumulative portion size and energy density were derived from 24-h dietary recall questionnaires at baseline and follow-up. BMI, whole-body fat percentage and fat-free mass were included as outcomes. Contrary to predictions, linear multiple regression models found some evidence of a negative, direct association between DVS and body weight outcomes at baseline (b = -0·13). Though dietary variety was significantly associated with larger portions across time points (b = 41·86-82·64), a moderated mediation effect was not supported at baseline or follow-up (Index ≤ 0·035). Taken together, these findings provide population-level evidence to support a positive association between variety and food intake, which in turn has potential implications for body weight management, both in terms of moderating food intake and benefitting diet quality.


Subject(s)
Biological Specimen Banks , Portion Size , Humans , Body Mass Index , Prospective Studies , Energy Intake , Body Weight , Diet , United Kingdom
3.
Foods ; 11(12)2022 Jun 10.
Article in English | MEDLINE | ID: mdl-35741901

ABSTRACT

Overconsumption of meat has been recognised as a key contributing factor to the climate emergency. Algae (including macroalgae and microalgae) are a nutritious and sustainable food source that may be utilised as an alternative to animal-based proteins. However, little is known about the consumer awareness and acceptance of algae as a protein alternative. The aim of this qualitative study was to develop a rich and contextualised understanding of consumer beliefs about the use of algae in novel and innovative food products. A total of 34 participants from the UK assisted with our study. Each participant engaged in one focus group, with six focus groups conducted in total. Existing consumer knowledge of algae was discussed before participants explored the idea of algae-based food products. Reflexive (inductive) thematic analysis was used to analyse these data. Results showed that consumers have limited pre-existing knowledge of algae as a food source; however, participants were open to the idea of trying to consume algae. This anticipated acceptance of algae was influenced by several product attributes, including perceived novelty, edibility, healthiness, sustainability, and affordability. These findings highlight algae as a promising protein alternative to support plant-forward diets in the UK and identify key attributes to consider in future product development and marketing strategies.

4.
Appetite ; 175: 106039, 2022 Aug 01.
Article in English | MEDLINE | ID: mdl-35429581

ABSTRACT

Previous research has suggested differences in psychological traits and eating behaviours between groups of individuals with varying weight management profiles, for example, differences between individuals who have maintained weight loss compared to those who have not. However, no study has looked at differences in traits across a sample with a broad range of characteristics including variations in bodyweight and its management. Across two studies, we identified and validated weight management profiles using a clustering approach and examined trait differences across groups. Data were collected using online questionnaires (Study 1: secondary data analysis; Study 2: primary data analysis allowing for cluster validation). Cluster analysis was implemented with BMI, diet history, weight suppression (difference between highest and current weight) as primary grouping variables, and age and gender as covariates. Differences in psychological and eating behaviour traits (e.g., restraint) were explored across clusters. In study 1, 423 participants (27.21 ± 9.90 years) were grouped into 5 clusters: 'lean men', 'lean young women', 'lean middle-aged women', 'successful' and 'unsuccessful dieters'. The cluster structure was broadly replicated with two additional groups identified ('lean women without dieting' and 'very successful dieters') in study 2 with 368 participants (34.41 ± 13.63 years). In both studies, unsuccessful dieters had higher restrained and emotional eating scores than lean individuals, and in study 1, they also had higher food addiction scores than successful dieters. Individuals could be grouped in terms of their weight management profiles and differences in psychological and eating behaviour traits were evident across these groups. Considering the differences in traits between the clusters may further improve the effectiveness and adherence of weight management advice.

5.
Appetite ; 168: 105718, 2022 01 01.
Article in English | MEDLINE | ID: mdl-34587544

ABSTRACT

Multi-component food-items are single food products that comprise more than one food class, brought together usually via some form of processing. Importantly, individual components of the food-item remain discernible and sensorially distinguishable from each other (e.g., chocolate chip cookies or 'choc ice'). Despite a sizable research literature on the formulation of such products, there lacks a concomitant research literature on the effect(s) of multi-component food-items (compared to single component food-items) on eating behaviour. Considerable previous research has investigated the effect of multiple separate food items on food intake, portion size selection and palatability. However, studies rarely use test foods that capture the physical or chemical interactions between components that are characteristic of multi-component foods. Nevertheless, previous research and relevant theory allow us to generate hypotheses about how multi-component foods may affect eating behaviour; consideration of food variety and perceived sensory complexity suggest that consumption of multi-component foods are likely to increase perceived palatability of such foods, self-selected portion size and food intake. Moreover, many (but not all) multi-component foods would be considered ultra-processed, which is a driver of food intake in and of itself. One possibility is that food components brought together as part of a multi-component food-item interact to strongly drive eating behaviour. To explore this idea, researchers will need to work across disciplines to address various practical and methodological barriers including the technical preparation of test foods.


Subject(s)
Feeding Behavior , Portion Size , Eating , Energy Intake , Food , Food Handling , Humans
6.
Pilot Feasibility Stud ; 7(1): 177, 2021 Sep 17.
Article in English | MEDLINE | ID: mdl-34535184

ABSTRACT

BACKGROUND: Portion size is known to be a key driver of food intake. As consumed portions are often pre-planned, 'ideal portion size'-an individual's preferred meal size selected prior to eating-has been identified as a strong predictor of actual consumption. However, assessments of ideal portion size have predominantly relied on laboratory-based computer tasks, limiting use online. Therefore, this cross-sectional study sought to pilot test the validity of a web-based tool to measure ideal portion size. METHODS: In an online study (N = 48), participants responded to images of a range of foods. Each food was photographed in a series of different portions and loaded into an 'image carousel' that would allow participants to change the size of the displayed portion by moving a slider left-to-right. Using this image carousel, participants selected their ideal portion size. They also completed measures of expected satiety and expected satiation and self-reported their age and body mass index (BMI). A non-parametric correlation matrix was used to explore associations between ideal portion size and identified predictors of food intake. RESULTS: Supporting convergent validity of this measure, ideal portion size was significantly correlated with expected satiety (rs = .480) and expected satiation (rs = -.310) after controlling for effects of baseline hunger and fullness, consistent with past research. Similarly, supporting divergent validity of this measure, ideal portion size was not significantly correlated with age (rs = -.032) or BMI (rs = -.111,). CONCLUSIONS: Pilot results support the validity of this web-based portion size selection tool used to measure ideal portion size, though further research is needed to validate use with comparisons to actual food intake.

7.
BMC Public Health ; 20(1): 1449, 2020 Sep 24.
Article in English | MEDLINE | ID: mdl-32972376

ABSTRACT

BACKGROUND: 'Food variety' is a key term that is frequently used in dietary guidelines around the world. Consuming a variety of foods - be it within a meal, across meals, or as part of the whole diet - is one factor that has been shown to increase food intake. However, little is known about consumer understanding of variety, and this may be a potential barrier to the success of dietary guidelines in today's 'obesogenic' environment. This research sought to explore 1) consumer recognition of different forms of variety, and 2) consumer definitions of variety. METHODS: In an online study (N = 240), participants were asked to discuss a range of photographs depicting different forms of variety, and to directly define the term 'food variety'. They were unaware of the research aim. RESULTS: Using a mixed methods approach, directed content analysis of these data showed that individuals referenced multiple forms of variety in the presence of food photographs. However, when asked to define variety, participants tended to only discuss variety in the context of the whole diet. CONCLUSIONS: These findings emphasise a need to educate consumers about variety to encourage adherence to dietary guidelines and help consumers better manage their own food intake.


Subject(s)
Diet , Meals , Consumer Behavior , Food Preferences , Humans , Perception , United Kingdom
8.
Appetite ; 147: 104504, 2020 04 01.
Article in English | MEDLINE | ID: mdl-31689448

ABSTRACT

Attachment orientation is a psychological factor concerning our expectations of ourselves and others in interpersonal relationships. An emerging literature has suggested that attachment orientation may influence a range of outcomes associated with bariatric surgery. The purpose of this scoping review was to map the literature and examine the role of attachment orientation in the context of bariatric surgery. Studies conducted with patients who are undergoing or have undergone bariatric surgery, with a measure of attachment orientation and published by 21st July 2019, were located through electronic searches including Scopus, PubMed and Web of Science. 21180 studies were identified, of which 18 were retained for narrative synthesis. The major outcome themes reported were (1) post-surgery weight-loss/body mass index (k = 10), (2) eating behaviour (k = 9), (3) attachment orientation differences in bariatric surgery patients compared with control groups (k = 4) and 4) other mental and physical health outcomes (k = 12). Overall, the results showed that there was little evidence to suggest that poor attachment orientation is predictor of weight-loss following surgery. There was evidence to suggest that poorer attachment orientation relates to poorer eating behaviours both before and after surgery, that patients undergoing bariatric surgery are more likely to have a poorer attachment orientation and attachment orientation is related to mental health outcomes but not physical health outcomes for patients. However, where relationships were identified, there were considerable inconsistencies regarding the dimension of attachment orientation that drove the relationship. Future studies should consider appropriate sample sizes for studies, replication of key findings and longer durations for longitudinal studies.


Subject(s)
Bariatric Surgery/psychology , Feeding Behavior/psychology , Obesity, Morbid/psychology , Object Attachment , Adult , Body Mass Index , Female , Humans , Male , Middle Aged , Obesity, Morbid/physiopathology , Obesity, Morbid/surgery , Outcome Assessment, Health Care , Postoperative Period , Treatment Outcome , Weight Loss
9.
Eur J Public Health ; 20(2): 231-5, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19667052

ABSTRACT

BACKGROUND: To investigate the association between breastfeeding duration and socio-economic status as measured by the English and Welsh Indices of Multiple Deprivation (IMD). METHODS: Total 216 multiparous women whose youngest or only child was between 6 and 24 months completed a retrospective questionnaire study of infant feeding between birth and 26 weeks. Measurements included breast-feeding history; socio-economic demography and IMD. RESULTS: Breastfeeding duration was associated with levels of multiple deprivation in both English and Welsh samples. Deprivation level and breastfeeding duration were associated with traditional indicators of socio-economic status. When considered in combination with other socio-economic indicators of breastfeeding duration, the deprivation level remained a strong predictor of breastfeeding duration over and above other socio-economic measures. CONCLUSIONS: Deprivation, as assessed by the IMD is predictive of breastfeeding duration. Postcode and thus deprivation level can be used as a non-intrusive way to identify women most at risk of low breastfeeding rates. Service provision can be targeted directly at women in areas recognized at being high in deprivation.


Subject(s)
Breast Feeding/epidemiology , England/epidemiology , Female , Humans , Socioeconomic Factors , Surveys and Questionnaires , Time Factors , Wales/epidemiology
10.
Eur J Neurosci ; 25(10): 3115-24, 2007 May.
Article in English | MEDLINE | ID: mdl-17561825

ABSTRACT

5-Hydroxytryptamine (5-HT)(2C) and 5-HT(1B) receptors are implicated in the inhibitory modulation of feeding behaviour. However, their respective, and possibly different, roles have not been clearly identified because of a lack of selective 5-HT(2C) receptor agonists. Here, using the putative, selective 5-HT(2C) receptor agonist VER23779, we show that its effects on feeding are fully reversed by pretreatment with a selective 5-HT(2C) receptor antagonist, but unaffected by pretreatment with either a 5-HT(1B) or a 5-HT(2A) receptor antagonist. In mice eating a palatable mash, feeding ends earlier, inactivity is increased but the behavioural satiety sequence is preserved. In a second-order schedule of reinforcement with an initial, non-food-reinforced appetitive phase, VER23779 produces a much greater relative reduction in appetitive responding than the 5-HT(1B) receptor agonist CP-94,253. Increased c-fos immunoreactivity patterns following VER23779 also differ from those described for CP-94,253, in particular showing strong activation of the basolateral amygdala. The different behavioural consequences of 5-HT(2C) and 5-HT(1B) receptor activation may relate to the patterns of c-fos immunoreactivity. In particular, the basolateral amygdala may have a role in maintaining response in the appetitive phase of the second-order schedule and also be susceptible to serotonergic modulation through activation of 5-HT(2C) receptors.


Subject(s)
Appetite/physiology , Brain/metabolism , Feeding Behavior/physiology , Proto-Oncogene Proteins c-fos/metabolism , Receptor, Serotonin, 5-HT2C/metabolism , Serotonin/metabolism , Amygdala/drug effects , Amygdala/metabolism , Animals , Appetite/drug effects , Brain/drug effects , Feeding Behavior/drug effects , Immunohistochemistry , Male , Mice , Mice, Inbred C57BL , Neural Inhibition/drug effects , Neural Inhibition/physiology , Receptor, Serotonin, 5-HT1B/drug effects , Receptor, Serotonin, 5-HT1B/metabolism , Satiety Response/drug effects , Satiety Response/physiology , Serotonin 5-HT2 Receptor Agonists , Serotonin 5-HT2 Receptor Antagonists , Serotonin Antagonists/pharmacology , Serotonin Receptor Agonists/pharmacology , Synaptic Transmission/drug effects , Synaptic Transmission/physiology , Up-Regulation/drug effects , Up-Regulation/physiology
11.
Eur J Neurosci ; 19(11): 3017-25, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15182309

ABSTRACT

Activation of 5-HT(1B) receptors is thought to play an important role in the inhibitory influence of serotonin on feeding behaviour and body weight in mammals. Earlier studies have shown that 5-HT(1B)-knockout (KO) mice eat more and are heavier than wild-type (WT) controls and that the selective 5-HT(1B) receptor agonist CP-94,253 reduces food intake in food-deprived mice. Here we characterize the behavioural effects of both CP-94,253 and the selective 5-HT(1B) receptor antagonist SB224289 on feeding and other behaviours within the behavioural satiety sequence, and also report a c-fos mapping study using CP-94,253. CP-94,253 produced a dose-dependent suppression of food intake with a profile consistent with a selective effect on feeding behaviour. These effects were absent or reduced in 5-HT(1B)-KO mice and in WT mice pretreated with SB224289. SB224289 administered alone enhanced food intake consistent with impaired satiation; a similar effect was apparent in 5-HT(1B)-KO mice compared to WT. CP-94,253 induced c-fos in a range of structures previously implicated in the expression of feeding behaviour. These results suggest that the activation of 5-HT(1B) receptors is an important component of endogenous satiation mechanisms in the mouse.


Subject(s)
Feeding Behavior/physiology , Proto-Oncogene Proteins c-fos/metabolism , Receptor, Serotonin, 5-HT1B/physiology , Animals , Behavior, Animal , Body Weight/drug effects , Body Weight/physiology , Brain/anatomy & histology , Brain/drug effects , Brain/metabolism , Dose-Response Relationship, Drug , Drug Interactions , Eating/drug effects , Feeding Behavior/drug effects , Gene Expression Regulation/drug effects , Immunohistochemistry/methods , Mice , Mice, Knockout , Oxadiazoles/pharmacology , Piperazines/pharmacology , Piperidones/pharmacology , Pyridines/pharmacology , Serotonin Antagonists/pharmacology , Serotonin Receptor Agonists/pharmacology , Spiro Compounds/pharmacology , Time Factors
12.
Psychopharmacology (Berl) ; 176(1): 39-49, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15138762

ABSTRACT

RATIONALE: The possible role of compensatory changes in 5-HT2C receptors in the reduced hypophagic action of d-fenfluramine in 5-HT1B knockout (KO) mice was assessed by comparing their response to d-fenfluramine and the 5-HT2C receptor agonist mCPP. In addition we measured 5-HT(2C/A) receptor binding in 5-HT1B KO and wild-type (WT) mice and examined the effects of 5-HT1B receptor antagonists on d-fenfluramine-induced hypophagia in WT mice. METHODS: Hypophagic responses to d-fenfluramine (1-30 mg/kg) and mCPP (1-5.6 mg/kg) were measured using a behavioural satiety sequence paradigm. The effects of the 5-HT1B receptor antagonists GR 127,935 and SB 224289 in opposing the hypophagic action of d-fenfluramine were evaluated in WT mice. The binding of [3H]-mesulergine was compared in the brains of both mouse strains. RESULTS: The hypophagic effects of moderate doses of d-fenfluramine and mCPP were attenuated in 5-HT1B KO mice. Pretreatment of WT mice with the 5-HT(1B/1D) receptor antagonist GR 127,935, or food-deprived WT mice with the 5-HT1B receptor antagonist SB 224289, did not reproduce the reduction in sensitivity to the effects of d-fenfluramine on feeding behaviour observed in 5-HT1B KO mice. Estimates of 5-HT2C receptor binding were similar in 5-HT1B KO and WT mice. CONCLUSIONS: The hypophagic effect of d-fenfluramine in mice is unlikely to be mediated by the 5-HT1B receptor. Instead, the evidence suggests that an adaptive change in 5-HT2C receptor function occurs in 5-HT1B receptor KO mice and contributes to their reduced response to d-fenfluramine.


Subject(s)
Fenfluramine/pharmacokinetics , Mice, Knockout/genetics , Piperazines/pharmacokinetics , Receptor, Serotonin, 5-HT1B/deficiency , Receptor, Serotonin, 5-HT1B/genetics , Satiation/drug effects , Serotonin 5-HT2 Receptor Agonists , Animals , Binding Sites/drug effects , Binding Sites/physiology , Cerebral Cortex/drug effects , Cerebral Cortex/metabolism , Cerebral Cortex/ultrastructure , Dose-Response Relationship, Drug , Drug Administration Schedule , Drug Evaluation, Preclinical/methods , Eating/drug effects , Ergolines/administration & dosage , Ergolines/pharmacokinetics , Fenfluramine/administration & dosage , Genotype , Injections, Intraperitoneal , Injections, Subcutaneous , Isomerism , Mianserin/pharmacology , Mice , Piperazines/administration & dosage , Piperidones/administration & dosage , Piperidones/pharmacokinetics , Receptor, Serotonin, 5-HT2A , Receptor, Serotonin, 5-HT2C/administration & dosage , Satiation/physiology , Satiety Response/drug effects , Satiety Response/physiology , Species Specificity , Spiperone/pharmacology , Spiro Compounds/administration & dosage , Spiro Compounds/pharmacokinetics , Time Factors , Tritium , United Kingdom
13.
Eur J Neurosci ; 17(1): 185-90, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12534984

ABSTRACT

Although null mutant ('knockout') mice have provided valuable animal models to complement traditional approaches to psychopharmacology, such animals may also show complex adaptations to the induced mutation. Here we demonstrate that serotonin1B (5-HT1B) receptor knockout (KO) mice show adaptations in serotonin2C (5-HT2C) receptor-mediated functions. They show smaller reductions in food intake and locomotor activity in response to administration of 5-HT2C receptor agonists that are not accounted for by altered drug disposition. These effects are not mimicked by pretreatment of wildtype (WT) mice with a 5-HT1B receptor antagonist showing that they result from a longer term adaptation to the loss of 5-HT1B receptor function and not from a short-term interaction between 5-HT1B- and 5-HT2C-mediated functions. In addition, we show that 5-HT1B receptor KO mice have a lowered hypothalamic c-fos response to the administration of 5-HT2C receptor agonists. These results demonstrate that compensatory adaptations to the constitutive loss of 5-HT1B receptors may be an important determinant of the altered response of 5-HT1B KO mice to a variety of pharmacological challenges.


Subject(s)
Hypothalamus/metabolism , Proto-Oncogene Proteins c-fos/metabolism , Receptors, Serotonin/deficiency , Receptors, Serotonin/metabolism , Animals , Cell Count , Dose-Response Relationship, Drug , Down-Regulation , Eating/drug effects , Ethylamines/pharmacology , Hypothalamus/drug effects , Indoles/pharmacology , Male , Mice , Mice, Knockout , Motor Activity/drug effects , Piperazines/pharmacokinetics , Piperazines/pharmacology , Proto-Oncogene Proteins c-fos/drug effects , Receptor, Serotonin, 5-HT1B , Receptor, Serotonin, 5-HT2C , Receptors, Serotonin/physiology , Serotonin Agents/pharmacology , Serotonin Receptor Agonists/pharmacology , Time Factors
14.
Eat Behav ; 4(4): 369-83, 2003 Nov.
Article in English | MEDLINE | ID: mdl-15000963

ABSTRACT

Previous laboratory studies of disinhibited eating in response to stress have had varied outcomes. Since recent research implies that disinhibited eating might be observed when using the Thre-Factor Eating Questionnaire restraint (TFEQ-R) measure when scores on the TFEQ disinhibition (TFEQ-D) scale were also used, the present study investigated the disinhibitory effects of stress on eating in women classified using both TFEQ-R [high R (HR) vs. low R (LR)] and TFEQ-D [high D (HD) vs. low D (LD)] scores. Twenty women in each restraint (R) or disinhibition (D) combination were tested in either a stress or no-stress condition followed by a test lunch. Women classified as LR-HD consumed more than the other groups in the no-stress condition and reduced intake in response to stress, whereas HR-HD and LR-LD both ate more in the stress than no-stress conditions. HD consumed more sweet foods regardless of stress, whereas HR ate less savoury foods than LR. Mood data confirmed the success of the stress manipulation on affective state and also suggested that HD were more responsive to stress. Overall, these data imply that tendency to overeat, as measured by the TFEQ-D scale, is a better predictor than restraint in predicting short-term eating in response to stress.

15.
Psychopharmacology (Berl) ; 164(1): 49-60, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12373419

ABSTRACT

RATIONALE: 5-HT(1B) receptors are thought to be one of the receptor subtypes that mediate the inhibitory control of serotonin on food intake and satiety. OBJECTIVE: To use the selective 5-HT(1B) receptor agonist, CP-94,253 as a probe of 5-HT(1B) receptor function in feeding behaviour, and to confirm the pharmacological selectivity of CP-94,253-induced hypophagia with a range of antagonists. METHODS: Dose-response functions for CP-94,253 (0, 1.25, 2.5, 5.0 mg/kg; IP) were determined in animals consuming wet mash in a 40-min test session during which time-sampled behavioural observations were collected to evaluate satiety sequences. A meal patterning study was carried out in a separate group of rats. The 5-HT(1A) antagonist WAY 100,635 (0, 1.0, 3.0 mg/kg; SC), the 5-HT(1B/1D)antagonist GR 127,935 (0, 3 mg/kg; IP), and the 5-HT(1B) antagonist SB 224289 (0, 2.5, 5.0 mg/kg; IP) were used to confirm that 5-HT(1B) receptor subtypes were responsible for the action of CP-94,253 on feeding behaviour. RESULTS: CP-94,253 (2.5 mg/kg) reduced food intake and preserved the satiety sequence in animals consuming a diet of mash. GR 127,935 (3.0 mg/kg) and SB 224289 (2.5 mg/kg), but not WAY 100,635, attenuated the hypophagic effect of the 5-HT(1B) agonist, and returned the changes in satiety sequence to control patterns. Meal patterning analyses indicated that CP-94,253 (2.5 mg/kg) reduced food intake through a decrease in meal size and duration in the absence of any alteration in the rate of eating. A hypodipsic action of CP-94,253 was also observed (2.5 and 5.0 mg/kg). CONCLUSION: These findings imply that 5-HT(1B) receptors regulate discrete elements of satiety. We discuss the potential role of 5-HT(1B) agonists for the treatment of obesity.


Subject(s)
Pyridines/pharmacology , Receptors, Serotonin/physiology , Satiety Response/drug effects , Serotonin Receptor Agonists/pharmacology , Animals , Dose-Response Relationship, Drug , Drinking/drug effects , Drinking/physiology , Eating/drug effects , Eating/physiology , Rats , Receptor, Serotonin, 5-HT1B , Satiety Response/physiology
16.
Pharmacol Biochem Behav ; 71(4): 691-700, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11888560

ABSTRACT

The studies reported here examined the role of the 5-hydroxytryptamine (5-HT)(2C) receptor subtype in the control of ingestive behaviour in mice. Behavioural satiety sequence (BSS) and food intake measurements were taken, comparing the selective 5-HT(2C) receptor agonist (S)-2-(6-chloro-5-fluoro-indol-l-yl)-l-methylethylamine hydrochloride (Ro 60-0175; 1.0, 3.0 and 10.0 mg/kg) and D-fenfluramine (3.0 mg/kg). Ro 60-0175 produced a dose-dependent decrease in food intake. The effects of Ro 60-0175 (3.0 mg/kg) on the BSS were similar to the hypophagic effects of D-fenfluramine (3.0 mg/kg). In a second experiment, the specific effects on feeding produced by Ro 60-0175 (5.6 mg/kg) were attenuated by pretreatment with the selective 5-HT(2C) receptor antagonist 6-chloro-5-methyl-1-[2(2-methylpyridyl-3-oxy)-pyrid-5-yl carbamoyl] indoline (SB 242084; 0.5 mg/kg). The 5-HT(1B/2C) receptor agonist 1-(m-chlorophenyl)piperazine (mCPP; 3 mg/kg) also produced a substantial decrease in food intake, which was attenuated by SB 242084 (0.5 mg/kg). A dose of the selective 5-HT(1B/1D) antagonist 2'-methyl-4'(5-methyl-[1,2,4]oxadiazol-3-yl)-biphenyl-4-carboxylic acid [4-(5-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]amide (GR 127935; 3.0 mg/kg) that successfully attenuated the action of the 5-HT(1B) agonist 5-methoxy-3(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (RU 24969; 5.0 mg/kg) failed to attenuate mCPP-induced hypophagia. These data suggest that Ro 60-0175- and mCPP-induced hypophagia in mice are mediated via activation of 5-HT(2C) receptors and that stimulation of 5-HT(1B) receptors plays only a minor role in mCPP-induced hypophagia.


Subject(s)
Receptors, Serotonin/drug effects , Satiety Response/drug effects , Serotonin Receptor Agonists/pharmacology , Aminopyridines/pharmacology , Animals , Diet , Dose-Response Relationship, Drug , Ethylamines/pharmacology , Feeding Behavior/drug effects , Indoles/pharmacology , Mice , Oxadiazoles/pharmacology , Piperazines/pharmacology , Receptor, Serotonin, 5-HT1B , Receptor, Serotonin, 5-HT2C , Serotonin Antagonists/pharmacology
17.
Pharmacol Biochem Behav ; 71(1-2): 147-54, 2002.
Article in English | MEDLINE | ID: mdl-11812517

ABSTRACT

Selective dopamine D(2) antogonists increase meal size and decrease the rate of feeding within a meal. Three experiments investigated the extent to which the atypical antipsychotics, clozapine and olanzapine, and the prototypical antipsychotic, haloperidol, affected meal size and feeding rate. Microstructural analyses of meal patterning were made over a range of drug doses administered to free feeding male Lister hooded rats. Haloperidol and clozapine produced a short-term increase in food intake. Haloperidol (0.05-0.2 mg/kg) enhanced meal size (maximal at 0.1 mg/kg) and reduced feeding rate (monotonic decrease with increasing dose). Neither clozapine (1-10 mg/kg) nor olanzapine (0.3-3 mg/kg) enhanced meal size, although both drugs produced similar reductions in feeding rate to haloperidol. These data suggest that enhancement of meal size may be correlated with a high level of extrapyramidal side effects in an antipsychotic drug. The absence of an increase in meal size by two atypical compounds suggests that the increase in body weight associated with clinical treatment with these drugs cannot be modelled by acute stimulation of meal size in the rat.


Subject(s)
Antipsychotic Agents/pharmacology , Clozapine/pharmacology , Feeding Behavior/drug effects , Haloperidol/pharmacology , Pirenzepine/analogs & derivatives , Pirenzepine/pharmacology , Animals , Antipsychotic Agents/adverse effects , Basal Ganglia Diseases/chemically induced , Benzodiazepines , Clozapine/adverse effects , Dose-Response Relationship, Drug , Eating/drug effects , Eating/physiology , Feeding Behavior/physiology , Haloperidol/adverse effects , Male , Olanzapine , Pirenzepine/adverse effects , Rats
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