Anne Raben, Lisa Agerholm-Larsen, Anne Flint, Jens J Holst, Arne Astrup, Meals with comparable vitality densities however wealthy in protein, fats, carbohydrate, or alcohol have completely different results on vitality expenditure and substrate metabolism however not on urge for food and vitality consumption, The American Journal of Medical Diet, Quantity 77, Challenge 1, January 2003, Pages 91–100, https://doi.org/10.1093/ajcn/77.1.91
ABSTRACT
INTRODUCTION
The prevalence of weight problems is growing dramatically, making a rising world well being downside (1). Weight problems is considered a multifactorial dysfunction. Two main causes of the event of chubby and weight problems are a discount in bodily exercise and a rise in vitality consumption, primarily from fat-rich, energy-dense meals (1). Within the vitality stability equation, vitality consumption might be way more delicate to dietary adjustments than is vitality expenditure (2, 3). The mechanisms concerned within the regulation of meals consumption are, nevertheless, advanced and suggest a number of completely different mechanisms, involving inside in addition to exterior elements. Some are macronutrient associated (eg, glucostatic and lipostatic mechanisms) and others are associated to hormones and afferent indicators [eg, insulin, glucagon-like peptide 1 (GLP-1), and leptin]. Moreover, vitality density (kJ/g) in all probability has a robust preabsorptive impact on meals consumption and thereby on vitality consumption (4).
The measured thermic impact of separate vitamins is highest and most extended for protein (20–30%), adopted by carbohydrate (5–10%) and fats (0–3%) (5, 6). The place of alcohol remains to be unclear. There additionally appears to be a line of proof suggesting a hierarchy in macronutrient oxidation charge through the postprandial state with the sequence alcohol > protein > carbohydrate > fats (3). Moreover, protein could create greater satiety sensations than carbohydrate, which can be extra satiating than fats (7–11). This has due to this fact result in the suggestion {that a} excessive satiating effectivity of a macronutrient is expounded to its oxidation charge—with the place of alcohol nonetheless being unclear.
To our data, all 4 macronutrients haven’t earlier than been included in a examine investigating their results on urge for food, vitality consumption and expenditure, and macronutrient metabolism on the identical time. The aim of the current examine was due to this fact to research the consequences of meals wealthy in both protein, carbohydrate, fats, or alcohol on postprandial vitality and substrate metabolism, subjective urge for food sensations, and advert libitum vitality consumption. Blood samples have been taken in one-half of the topics for substrate and hormone analyses to clarify doable variations within the main consequence variables. Younger, normal-weight ladies and men have been included.
SUBJECTS AND METHODS
Experimental design
The examine used a crossover design through which baseline and postprandial variables have been measured over a interval of 5 h after consumption of the 4 take a look at meals. The take a look at meals got in random order to the topics on separate days with ≥ 4 wk and not more than 8 wk separating the take a look at days. The themes weren’t allowed to have interaction in strenuous bodily exercise for two d earlier than the take a look at day. The day earlier than every take a look at day, topics got a person standardized, weight-maintenance, carbohydrate-rich food regimen for 1 d. These measures have been taken to make sure equally crammed glycogen shops and comparable macronutrient stability in every particular person on the 4 completely different take a look at days (12).
Topics
In line with our earlier reproducibility examine on urge for food scores, 8–15 topics are wanted to acquire statistically vital variations in imply postprandial scores when utilizing a crossover design (13). To account for dropouts, 20 wholesome topics (10 feminine and 10 male) have been enrolled after announcement on the Royal Veterinary and Agricultural College and the College of Copenhagen. Inclusion standards have been as follows: aged 20–30 y; regular weight (physique mass index, in kg/m2, > 18.5 however < 25.0); nonsmoker; not an elite athlete; regular alcohol habits; no historical past of weight problems, diabetes, or liver illnesses; regular blood strain; and no common use of medicines (aside from contraception tablets). Earlier than coming into the examine, the topics have been screened to make sure that they fulfilled the inclusion standards. The ladies have been screened for an everyday menstrual cycle, and through the examine the 4 separate take a look at days have been positioned on the identical time of the ladies's cycle (between days 7 and 11 within the follicular section) in order that hormonal fluctuations wouldn't have an effect on the measurements (14, 15). Blood samples have been collected through the take a look at days from 10 randomly chosen topics (5 girls, 5 males). All topics gave written consent after the experimental process had been defined to them. The examine was authorized by the Municipal Moral committees of Copenhagen and Frederiksberg to be in accordance with the Helsinki-II declaration. Of the 20 enrolled topics, 1 topic (a lady) was excluded due to sickness (migraine) on a take a look at day. Thus, 19 topics accomplished the examine and carried out 4 take a look at days every. The topic traits are offered in Desk 1. Diets The usual food regimen contained 49.2% of vitality as carbohydrate, 37.4% of vitality as fats, 13.2% of vitality as protein, and 1.7 g dietary fiber/MJ, and had an vitality density of 8.5 kJ/g. The food regimen was ready on the Analysis Division of Human Diet from regular Danish meals gadgets in response to every topics' particular person vitality necessities, adjusted to the closest 0.5 MJ. The themes' vitality necessities for the usual food regimen and the take a look at meals have been decided through the use of World Well being Group tables in response to age, weight, and intercourse (16). We used the multiplication elements of 1.64 for ladies and 1.78 for males to account for the medium bodily exercise of the topics. The themes have been instructed to stick strictly to the usual food regimen. 4 completely different take a look at meals wealthy in protein, carbohydrate, fats, or alcohol, respectively, have been examined in a randomized order (Desk 2). Dietary fiber content material and vitality density have been an identical in all 4 meals. The take a look at meals provided contained 2500 kJ (26% of vitality expenditure) for ladies and 3000 kJ (22% of vitality expenditure) for males. The protein-rich meal consisted of crisp bread with cheese, yogurt with muesli, boiled egg, and skim milk. The carbohydrate-rich meal consisted of corn flakes with skim milk, white bread with butter, cheese, jam, and honey. The fat-rich meal consisted of yogurt blended with double cream and grated apple, honeydew melon, rye bread with butter, cream cheese, and complete milk. The alcohol-rich meal consisted of rye bread and whole-grain bread with butter and cheese, yogurt with muesli, honeydew melon, and orange juice with vodka. Males got 24 g and girls 20 g alcohol. The identical time (a most of 15 min) was spent on the meal on every take a look at day. On the finish of the take a look at day, the topics have been provided a sizzling lunch meal advert libitum in a eating room on the division. The meal consisted of pasta and meat sauce with greens and was provided in 6- and 8-MJ variations for ladies and men, respectively. The take a look at meal contributed 13.3% of vitality as protein, 50.0% of vitality as carbohydrate, 36.8% of vitality as fats, 0.7 g dietary fiber/MJ, and eight.2 kJ/g. Topics have been instructed to eat as a lot as they wished to really feel comfortably satiated. The trainer registered the quantities eaten through the use of a digital meals weight. The pc database of meals from the Nationwide Meals Company of Denmark (Dankost 2.0) was used within the calculations of vitality and nutrient composition of the diets. Experimental protocol On the take a look at day, the topics arrived on the division at 0800 with a minimal of exercise (by automobile or bus) and after having fasted for 10 h from the night earlier than. After the topics voided, physique weight was measured (to the closest 100 g) with topics carrying underwear and through the use of the identical digital scale every time (SECA mannequin 707; Seca, Copenhagen). Physique composition was subsequently estimated by bioelectrical impedance with an Animeter (HTS-Engineering Inc, Odense, Denmark). For one-half of the topics, a Venflon catheter (Viggo, Gothenburg, Sweden) was inserted in an antecubital arm vein. The themes then rested for 30 min in a supine place on a mattress coated with an antidecubitus mattress and with a slight elevation of the pinnacle, and resting metabolic charge was measured for 45 min (0845–0930). A fasting blood pattern was taken at 0935–0940.
The meal was served at 0945 (time = 0) and was consumed inside 15 min. Precisely the identical time was spent on the 4 take a look at meals for every particular person topic. Earlier than, after (at 1000), and each 30 min till 5 h after the meal (at 1500), questionnaires to evaluate starvation, satiety, fullness, potential meals consumption, and needs for one thing salty, candy, or fatty or for meat or fish have been crammed out by every topic. Scores have been made on 10-cm visible analogue scales (VAS scores) offered as a small folder with one query per web page. Phrases have been anchored at every finish of the VAS, expressing probably the most constructive (ie, good, nice) or probably the most adverse (dangerous, disagreeable) score (13, 17). Instantly after the take a look at meal, topics recorded their analysis of style, aftertaste, scent, visible enchantment, and general impression of the take a look at meals by VAS scores. Postprandial blood samples have been taken at 15, 45, 75, 105, 135, 165, 195, 255, 285, and 315 min from meal initiation. Through the postprandial section (15–315 min), vitality expenditure was measured constantly. The themes have been allowed to observe mild leisure motion pictures and to have small breaks of ≈5 min as soon as each hour if wanted. Through the break the topics may lie down in a supine place with out the hood, sit, stroll quietly, or go to the bathroom if wanted. All urine, besides morning urine, was pooled in the identical container through the whole 7-h measurement interval (800–1500) for later nitrogen analyses. A minor quantity of water consumption was allowed through the take a look at day (most: 200 mL), however the whole quantity consumed was famous along with the breaks, and each situations have been repeated on the following 3 take a look at days. Vitality expenditure and oxidation charges The speed of protein oxidation was assumed to be fixed all through the take a look at day. One gram nitrogen was assumed to correspond to six.25 g protein, and ≈81% of the ingested nitrogen was assumed to be excreted within the urine (20). Protein oxidation ought to have been calculated for every particular person take a look at interval. Nevertheless, as a result of we didn't have full nitrogen information from all topics (n = 16–18 per meal), we determined to make use of the identical imply worth of nitrogen for a person for the 4 take a look at meals. The error was in all probability small, as a result of the typical nitrogen recovered for the 4 meals was comparable (vary: 2.89–3.09 g; NS). Alcohol was assumed to be completely oxidized through the 5-h postprandial measurements (19, 21, 22), and its oxidation charge was estimated to be fixed with 1.89 kJ/min (totaling 595.4 kJ/315 min) for ladies and a pair of.26 kJ/min (totaling 711.9 kJ/315 min) for males. Laboratory evaluation Blood was sampled with out stasis by way of an indwelling catheter into iced syringes. Inside 30 min, samples have been centrifuged for 10 min at 3000 × g and 4 °C, and the supernatant fluid was saved at −80 or −20 °C till analyzed. Blood for dedication of plasma glucose and lactate was collected in fluoride-EDTA ready tubes (Vacurette; Greiner labortechnik, Kremsmoenster, Austria) and was analyzed by commonplace endpoint enzymatic strategies (MPR3 Gluco-Quant Glucose/HK and MPR3 Hexokinase/G&P-DH take a look at kits; Boehringer Mannheim GmbH Diagnostica, Copenhagen) (23, 24). Serum was extracted for the evaluation of nonesterified fatty acids, and the extracts have been saved at −20 °C till later evaluation by an enzymatic, quantitative colorimetric technique (Wako NEFA take a look at equipment, NEFA C, ACS-ACOP technique; Wako, Interkemi, Denmark). Serum triacylglycerol was extracted and measured by an enzymatic endpoint technique [Test-Combination Triacylglycerol (GPO-PAP) kit, Boehringer Mannheim, GmbH-Diagnostica] (25). Insulin was measured towards requirements of mouse monoclonal antibodies by immunoassay (DAKO insulin, enzyme-linked immunosorbent assay technique; DAKO, Cambridgeshire, United Kingdom) (26). A Cobas Mira (Roche Diagnostica System, Basel, Switzerland) was used to research these samples. For dedication of the concentrations of the hormones glucagon, glucose-dependent insulinotropic polypeptide (GIP), GLP-1, glucagon-like peptide 2 (GLP-2), and leptin, blood was sampled in syringes containing EDTA and aprotinin. Plasma was saved at −20 °C. Earlier than evaluation the samples have been extracted by ethanol. The focus of GIP was decided through the use of human GIP and 125I-labeled human GIP as requirements and tracer (27). GLP-1 was measured towards requirements of an artificial GLP-1 amide particular for the carboxyl-terminal finish of GLP-1, which reacts with GLP-1 of intestinal origin (28). GLP-2 was measured through the use of an antiserum towards the amino terminus of human GLP-2, which measures solely absolutely processed, nondegraded GLP-2 (29). Leptin was decided in serum with a human leptin radioimmunoassay equipment (DRG Diagnostic, Marburg, Germany) (30, 31). Urine quantity was decided, and nitrogen focus was measured with a nitrogen analyzer (NA 1500; Carlo Erba Strumentazione, Milan, Italy) (32). Statistical analyses All outcomes are given as means ± SEMs. Postprandial values are expressed as adjustments from fasting values. Response curves after the 4 take a look at meals have been in contrast by evaluation of variance (ANOVA) with the GLM process in SAS (model 6.12; SAS Institute Inc, Cary, NC). We examined for meal × time × intercourse, meal × intercourse, and meal × time interactions and the consequences of time, intercourse, and meal individually. Topic (meal) was used as an error time period for meal results. Submit hoc exams have been executed on least-squares means through the use of Tukey changes for a number of comparisons. Space below (or above) the curves, Δ-AUC, was calculated individually for every topic because the distinction between the built-in space of the response curve and the oblong space decided by the basal values. Unfavorable (or constructive) areas have been included. For urge for food scores, the imply change in postprandial scores from fasting stage, Δ-mean, was calculated. The extent of statistical significance was set at P < 0.05. STATGRAPHICS software program (model 4.2; Graphic Software program Techniques, Inc, Rockville, MD) and SAS (SAS Institute Inc) have been used for the statistical calculations.RESULTS
Analysis of the take a look at meals
The questionnaire, given to the topics instantly after they consumed the take a look at meals, confirmed that each the ladies and the boys evaluated the take a look at meals alike. The scores for general look and scent weren’t considerably completely different between the 4 take a look at meals (Desk 3). Nevertheless, the topics discovered that the alcohol meal had a extra disagreeable style and was much less appetizing general than was the carbohydrate meal and had extra aftertaste than did the opposite 3 meals.
Satiety scores
There have been no vital variations in postprandial sensations of starvation or satiety (Determine 1) or in potential meals consumption and fullness (information not proven) after the 4 meals. Nevertheless, need for one thing candy confirmed a big interplay between meal and time (P < 0.05), with an initially decrease need after the carbohydrate meal and the next need after the protein meal (Determine 1). The themes' need for some meat or fish confirmed an interplay between time, intercourse, and meal (P < 0.0001; Determine 1). The Δ-mean scores weren't considerably completely different between the meals (Desk 4), however the girls reported to be much less hungry and extra full than did the boys (intercourse impact: P < 0.05), and the boys had the next need for one thing fatty than did the ladies (intercourse impact: P < 0.05).
Advert libitum vitality consumption As a result of the evaluations of the breakfast meals have been completely different, these evaluations have been included as covariates within the statistical evaluation of the next advert libitum consumption. There was a meal × intercourse impact for advert libitum vitality consumption (P < 0.05; Determine 2), however publish hoc exams confirmed no vital variations between meals for every intercourse individually. On common, vitality consumption was twice as excessive within the males as within the girls (intercourse impact: P < 0.001). Vitality expenditure and substrate oxidation Postprandial vitality expenditure was initially highest after the alcohol meal, however on the finish, vitality expenditure was highest for the protein meal (meal × time impact: P <0.001; Determine 3). Common DIT was 17% greater after the protein meal (NS) and 27% greater after the alcohol meal (P < 0.01) than after the carbohydrate and fats meals (meal impact: P <0.01; Determine 3). When expressed as a share of vitality consumption, DIT averaged 8.3% after the protein meal, 9.0% after the alcohol meal, and seven.1% after each the fats and carbohydrate meals (meal impact: P < 0.01). There have been no intercourse or intercourse × meal results. The carbohydrate oxidation curve was highest and lasted the longest after consumption of carbohydrate (meal × time impact: P < 0.0001; Determine 3). Likewise, the Δ-AUC was 2–3 instances bigger after the carbohydrate meal than after the opposite 3 meals (meal impact: P < 0.0001; Determine 3). Postprandial fats oxidation was initially enormously suppressed after each the carbohydrate and alcohol meals in contrast with the fats and protein meals, and remained suppressed after the alcohol meal (meal × time impact: P < 0.0001; Determine 3). The Δ-AUC was considerably decrease after the alcohol meal than after the carbohydrate meal and was nearly unchanged after the fats and protein meals (meal impact: P < 0.0001; Determine 3). Glucose, lactate, insulin, and glucagon Postprandial plasma glucose elevated extra after the carbohydrate meal than after the opposite 3 meals (meal × time impact: P < 0.0001; Determine 4). Glucose decreased barely beneath fasting concentrations after the protein, fats, and alcohol meals however not after the carbohydrate meal. The Δ-AUC was additionally highest after the carbohydrate meal in contrast with the opposite meals (meal impact: P <0.001). There was a bent towards a distinction in response between the sexes, with a 3 instances greater imply focus within the girls than within the males (intercourse impact: P = 0.053; information not proven). The postprandial lactate response confirmed an interplay between meal and time (P < 0.0001; Determine 4), with the best focus after the carbohydrate meal adopted by the alcohol meal. The Δ-AUCs have been additionally completely different between meals, with the next Δ-AUC after each the carbohydrate and alcohol meals than after the fats and protein meals (meal impact: P < 0.0001). The plasma insulin response confirmed the best improve after the carbohydrate meal adopted by the alcohol meal (meal × time impact: P < 0.01; Determine 4). There was additionally a big time × intercourse impact (P < 0.05), with steeper will increase within the girls than within the males (information not proven). The insulin Δ-AUCs have been highest after the carbohydrate meal and lowest after the fats meal (meal impact: P < 0.0001). On the whole, Δ-AUCs have been twice as excessive within the girls as within the males (intercourse impact: P < 0.01; information not proven). Glucagon concentrations have been discovered to be nearly unchanged from fasting concentrations after the carbohydrate meal, however elevated after the three different meals, though with completely different time patterns and a late peak after the alcohol meal (meal × time impact: P < 0.0001; Determine 4). A major distinction within the Δ-AUCs was discovered, with excessive responses after the protein, fats, and alcohol meals and a adverse Δ-AUC after the carbohydrate meal (meal impact: P < 0.0001). The imply glucagon Δ-AUC was 5 instances greater within the males than within the girls (intercourse impact: P < 0.001; information not proven). Triacylglycerol, nonesterified fatty acids, and leptin For triacylglycerol, interactions between meal and time (P < 0.0001) and time and intercourse (P < 0.05) have been noticed (Determine 5). The fats and alcohol meals induced the best responses, though the alcohol meal precipitated a slower postprandial improve. The Δ-AUCs for triacylglycerol have been additionally bigger after the fats and alcohol meals than after the protein and carbohydrate meals (meal impact: P < 0.0001; Determine 5). On the whole, plasma nonesterified fatty acids decreased from fasting concentrations after the onset of all 4 meals, however extra so and with a later return to fasting concentrations after the protein and carbohydrate meals (meal × time impact: P <0.05; Determine 5). The Δ-AUC was decrease after the protein meal than after the fats meal (P < 0.05). For leptin, a big interplay was noticed between meal, time, and intercourse (P < 0.001) and between time and meal (P < 0.0001). A marked suppression was seen the primary 4 h after the alcohol meal in contrast with a slight suppression the primary 3 h after the opposite meals (Determine 5). The Δ-AUC for leptin was considerably decrease after the alcohol meal than after the protein and carbohydrate meals (meal impact: P <0.05). GIP, GLP-1, and GLP-2 The GIP response confirmed an interplay between meal and time (P < 0.0001) and meal and intercourse (P < 0.05; Determine 6). The fats meal produced probably the most fast and steepest response curve, adopted by the carbohydrate meal. The Δ-AUCs have been highest after the fats meal, adopted by the carbohydrate meal (meal impact: P < 0.0001; meal × intercourse interplay: P < 0.05). The ladies had a decrease GIP than did the boys after the protein meal (P < 0.05; information not proven). GLP-1 confirmed an interplay between meal and time (P < 0.0001; Determine 6). The protein meal gave the best response, whereas the alcohol meal induced each a decrease and slower response in contrast with the opposite meals. The protein meal created the best Δ-AUC, adopted by the carbohydrate meal, and the alcohol meal produced the bottom Δ-AUC (meal impact: P < 0.01). GLP-2 was nearly unchanged after the alcohol meal, however elevated after the fats and protein meals (meal × time impact: P < 0.001; Determine 6). After the carbohydrate meal, GLP-2 elevated much less and appeared to succeed in a plateau 1 h after the meal. The Δ-AUCs confirmed a distinction between the meals (P < 0.05), with the best Δ-AUCs after the protein and fats meals.DISCUSSION – “like proteins carbohydrates and fat alcohol”
Food plan-induced thermogenesis
A transparent discovering within the current examine was a 27% bigger DIT after the alcohol meal than after the carbohydrate and fats meals. DIT was additionally bigger after protein meal (by 17%), however this was not considerably completely different from the opposite meals. That DIT remained elevated after the alcohol and protein meals on the finish of the 5-h measurement interval means that the consequences of those meals might need been extra pronounced had our measurement interval been longer. The excessive DIT after the alcohol meal is presumably associated to the reoxidation of cytoplasmic NADH not being tightly linked to ATP technology. Alcohol oxidation begins immediately after consumption, and alcohol is ultimately utterly eradicated by oxidation (22, 33). Nonetheless, the outcomes of earlier research aren’t concordant on the magnitude of DIT after alcohol consumption, and reported DIT values vary between 9% and 28% (22, 34–36). Moreover, a long-term examine reported comparable metabolizable vitality after alcohol and carbohydrate (37), so discrepancies do exist.
Though DIT was 17% greater after the protein meal, it was not considerably elevated in contrast with the carbohydrate and fats meals. The dearth of a bigger DIT after the protein meal, as was anticipated from earlier ideas (5) and short-term research (38–40), could relate to using a extra stringent publish hoc take a look at (Tukey’s) within the current than within the earlier research or to using extra compound meals as an alternative of single macronutrients. The dearth of distinction in DIT between the fats and carbohydrate meals was, nevertheless, much like different research through which the ratio of fats to carbohydrate was manipulated (41, 42). On the premise of the current 5-h outcomes, our oxidation hierarchy might be summarized as follows: alcohol > protein = fats = carbohydrate.
Urge for food and advert libitum consumption
We have been unable to indicate vital variations within the subjective sensations of satiety, starvation, fullness, or potential meals consumption in our examine. VAS scores may due to this fact not be used to indicate the satiety hierarchy of protein > carbohydrate > fats. Nor may we suggest a place for alcohol on this hierarchy on the premise of the VAS scores. The dearth of variations was considerably stunning as a result of greater satiety after protein than after carbohydrate and fats has been proven earlier than (7, 8, 11, 43, 44), though not constantly (45–48). Our use of meals with comparable vitality densities may, nevertheless, be a significant purpose for the shortage of variations in starvation and satiety scores (4). Discrepancies within the earlier examine outcomes in all probability relate to completely different strategies, eg, using fluid moderately than strong meals, variations in vitality masses (an quantity > 1.5 MJ could also be wanted), preload versus take a look at meal, completely different measurement intervals, and variations in topic traits (reminiscent of intercourse, age, and physique mass index).
It was fascinating to notice that through the first interval after breakfast, the topics had a decrease need for one thing candy after the carbohydrate meal and the next need for one thing candy after the protein meal. This phenomenon in all probability displays sensory-specific satiety (45). A carbohydrate-rich food regimen could due to this fact lower the urge for candy snacks between meals.
We didn’t observe any vital variations in advert libitum vitality consumption after the 4 meals. On the premise of earlier research, we had anticipated to discover a decreased vitality consumption after the protein meal (10, 43–45) in contrast with the carbohydrate and fats meals. This could even have been in step with the outcomes of a 6-mo advert libitum examine exhibiting a higher discount in physique weight after a low-fat, high-protein food regimen than after a low-fat, high-carbohydrate food regimen (49) and with the findings of routine protein consumption being negatively correlated with vitality consumption (50). That protein didn’t suppress vitality consumption right here is, nevertheless, in settlement with different short-term research (7, 11, 46, 51).
In our examine, the impact of the alcohol-rich meal on vitality consumption was not considerably completely different from the consequences of the opposite meals. Thus, alcohol didn’t stimulate vitality consumption, as was been reported when alcohol was given as an aperitif (52) or with dinner (B Buemann, S Toubro, A Astrup, unpublished observations, 2002). Different research didn’t, nevertheless, report any distinction in vitality consumption after alcohol in contrast with carbohydrate or fats consumption (53). When the alcohol is served could due to this fact play a job, ie, whether or not it’s given earlier than or with a meal, along with whether or not it’s given along with or as an alternative to different macronutrients. On the premise of our advert libitum information, we additionally couldn’t suggest a satiety hierarchy for the 4 macronutrients.
We noticed that vitality consumption was twice as excessive within the males as within the girls. As a result of the thermogenic response was comparable within the ladies and men, nonphysiologic mechanisms could have been concerned within the girls’s advert libitum meals consumption. These girls could have been steered by psychological mechanisms (dietary restraint and considerations about physique weight) moderately than physiologic wants for vitality. This speculation is supported by the outcomes of earlier research (54–56) and could also be particularly related as a result of our topics ate below supervision.
Substrates and hormones
As anticipated, carbohydrate oxidation was greater after the carbohydrate meal than after the opposite meals. This was additionally mirrored in greater postprandial glucose, lactate, and insulin concentrations after this meal. The suppression of fats oxidation and nonesterified fatty acids and the minor impact on triacylglycerol and glucagon all agree with the stimulation of insulin after carbohydrate consumption. Though each insulin and GLP-1 have been elevated after the carbohydrate meal, starvation and vitality consumption weren’t decrease after this food regimen than after the opposite meals, as might need been anticipated (57, 58).
After the alcohol meal, web fats oxidation was enormously suppressed, much more than after the carbohydrate meal. Additionally, carbohydrate oxidation was comparatively low after the alcohol meal contemplating the carbohydrate content material on this meal (43% of vitality). This was in all probability because of the destiny of acetate, the main product of ethanol metabolism within the liver (59). Acetate is launched to the circulation and primarily oxidized, in all probability with precedence over different substrates. Moreover, acetate launched into plasma inhibits lipolysis (59). We additionally noticed a rise in triacylglycerol, occurring later, however with as excessive a Δ-AUC as after the fats meal, regardless of a large distinction in fats consumption (24% in contrast with 65% of vitality). This improve may have been attributable to a stimulation of hepatic lipogenesis, growing the contribution of fatty acids to circulating VLDL-triacylglycerol (59). Leptin concentrations have been additionally enormously suppressed after the alcohol meal in distinction with the opposite 3 meals. This remark has not been printed earlier than within the literature. In distinction, routine alcohol consumption was reported to be positively related to circulating leptin in younger, wholesome males (60). Moreover, main adjustments in leptin are usually not seen acutely after meal consumption (61). The rationale could also be associated to the above-mentioned results of alcohol on fats metabolism, inflicting a suppression of leptin launch from adipose tissue. No or solely small results of alcohol have been seen on GIP, GLP-1, and GLP-2. This will relate to alcohol being largely absorbed by way of the abdomen wall and never coming into the small gut.
After the fats meal we noticed the anticipated improve in triacylglycerol, with a peak ≈3 h postprandially, whereas fats oxidation was nearly unchanged. Moreover, we noticed a rise in each GIP and GLP-2 after the fats meal. This will clarify why insulin elevated regardless of comparatively low carbohydrate (24% of vitality) and protein (12% of vitality) intakes with the fats meal. Fats consumption has been proven to stimulate GIP earlier than (62). The elevated GIP could activate lipoprotein lipase and thereby improve chylomicron clearance from the circulation (63).
The carbohydrate oxidation charge was low and fats oxidation nearly unchanged after the protein meal. Nevertheless, the protein meal suppressed nonesterified fatty acids as a lot as did the carbohydrate meal and stimulated GLP-1 and GLP-2. GLP-1 has been proposed to have satiating properties (58), however the variations right here have been apparently not massive sufficient to supply variations in urge for food scores or advert libitum vitality consumption.
Conclusion
The next thermogenic response was noticed after a meal wealthy in alcohol than after meals wealthy in protein, fats, or carbohydrate with comparable vitality densities and dietary fiber contents. Regardless of measurable variations in substrate oxidation, plasma substrates, and hormones, we noticed no vital variations in subjective starvation and satiety sensations or in advert libitum vitality consumption. Our information from compound meals, due to this fact, don’t help the existence of a satiety hierarchy resembling the oxidative hierarchy of the 4 macronutrients. The apparently constructive results of alcohol on vitality expenditure needs to be thought of along with the enormously suppressed fats oxidation and leptin concentrations and elevated triacylglycerol concentrations after the alcohol meal. The response patterns in a 5-h interval may change if longer measurement intervals are used
We gratefully thank Ulla Pedersen, Inge Timmermann, Jannie Møller Larsen, Lars Paaske, John Lind, Charlotte Kostecki, and Trine Jessen from the Analysis Division of Human Diet for skilled technical help and the topics for his or her prepared participation.
REFERENCES
FOOTNOTES
“like proteins carbohydrates and fat alcohol”