Coconut Oil (Lauric
Acid) - Weight Loss and
Anti-Inflammation Nutritional Benefits of MCT, Medium Chain
Triglycerides
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Coconut Oil contains a special kind of saturated fat that is usually
healthy to eat, called lauric acid, with a mixture of MCT fats
called medium chain triglycerides (which may have from 8 to 12
carbon atoms). While these fats are "saturated" with hydrogen atoms,
they often act differently in the human body than other, longer
saturated fats. Lauric Acid is a medium-chain triglyceride, with 12
carbon atoms (also called dodecanoic acid). These shorter-length
acid molecules, unlike many saturated fats, often actually SPEED UP
WEIGHT LOSS. They also may help reduce the risk for heart disease,
high blood pressure, and many other health problems. In some studies
MCT's have been shown to fight various infections, and help minimize
damage to organs from some drug therapies. Replacing other saturated
fats in your diet with a small daily amount of coconut oil is part
of our Food Guide Football eating plan.
Coconut Oil consists of medium chain fatty acids MCFA, such as
lauric acid. These fats contain only about 8, 10 or 12 carbon atoms,
instead of the 18 or 20 contained in other vegetable oils such as
corn oil, safflower oil, peanut oil, cottonseed oil, etc. As a
result of the shorter molecule length, the body does not need to use
a relatively scarce CPT enzyme as it does for the longer 18-20
carbon oils. Medium chain triglycerides from coconut oil are
digested rapidly in the liver, instead of circulating in the body
and being stored as fat tissue deposits.
For cooking, coconut oil has a higher smoke point than does butter.
It is also less sensitive to spoiling or becoming rancid, although
it should still be handled with care.
How Much Coconut Oil Should You Eat Per Day?
Studies support replacing other fats in your diet with coconut oil,
up to 2 or 3 tablespoons per day. It is important not to add more
oil into your diet, if possible. Instead, simply replace "long-chain
triglyceride" poly-unsaturated vegetable oils like corn, safflower,
cottonseed, sunflower and soybean oils with coconut oil. You may
continue to use extra virgin olive oils as usual -- trade coconut
oil for the other oils in your diet. If you have already removed the
other oils and you're using nothing but olive oil now, simply add a
total of two or three tablespoons of coconut oil to your drinks,
vegetables, salad dressings, and so on each day. Be creative... it's
healthy!
Which Kind Of Coconut Oil Is Best?
Avoid Hydrogenated or partially-hydrogenated coconut oil that is
often used in non-dairy creamers, and snack foods. Buy only "virgin
coconut oil" -- a natural, organic and purified coconut oil that has
never been "hydrogenated", heated or exposed to long storage and
other processing. Buy the freshest oil you can find. Be picky.
Lauric acid and other medium-chain fatty acids can spoil and become
horrible tasting; even becoming unhealthy if things go far enough.
Never store your coconut oil for more than 2 months. Refrigerate
after opening, if your room temperature often rises above 75
degrees. A cooler, dry, dark place inside a cabinet is usually a
good place, unless it is uncommonly warm. Don't keep coconut oil
near your oven or range. Store it only in tightly sealed screw-on or
snap-on lids. Glass bottles are preferred to plastic or metal
containers.
Where to buy Virgin Coconut Oil
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Coconut Oil Health Benefits
Over the last 40 years, scientific peer reviewed studies have shown
these benefits to coconut oil medium chain fatty acids:
(1,2,3,4,5...)
Fights many bacterial infections, including H.Pylori (the cause of
most ulcers) (43)
Fights many viral infections, including Vesicular Stomatitis Virus (VSV)
(44)
Increases daily energy expenditure (22)
Increases dietary taste and "mouth feel" appeal
Makes reduced portion size meals appetizing
Reduces overall food intake by extending post-meal satiation period
(37)
Improves overall glucose metabolism (27-34, 40)
Improves NIDDM (type 2 diabetes) glycemic metabolism, by increasing
insulin sensitivity and insulin controlled glucose disposal (40)
Normalizes weight gain, compared to corn oil (42)
Leads to reduced blood pressure
Reduces the number of fat cells, and amount of fats stored (36)
Obesity is caused by eating too much long-chain fatty acids
(vegetable oil); medium-chain fatty acids (as in coconut oil)
reverse this condition, reducing obesity (38)
Speeds up metabolism after meals (41)
Improves athletic endurance exercise performance (39)
Reduces liver's production of LDL "bad" cholesterol
Has no effect on production of HDL "good" cholesterol
Reduces circulating triglycerides and free fatty acids FFAs
Reduces intra-cellular lipids in muscle tissue, reducing insulin
resistance (35)
Accelerates or catalyzes burning and oxidation of other oils by the
liver
Absorbed from intestines directly into liver by portal vein
Does not circulate in blood like other vegetable oils
Rapidly oxidized or burned by the liver -- as fast as pure glucose
Does not require rate-limiting enzyme CPT (carnitine
palmitoyltransferase) for metabolism, as would long-chain fatty
acids found in vegetable oils
Results in steady weight loss for obese individuals, and weight
maintenance for healthy people
Peer Reviewed Scientific Studies of Coconut Oil, Lauric Acid,
and Medium Chain Triglycerides
1. JULY 2007: Effects of dietary medium-chain triglyceride on weight
loss and insulin sensitivity in a group of moderately overweight
free-living type 2 diabetic Chinese subjects. Authored by: Han JR,
Deng B, Sun J, Chen CG, Corkey BE, Kirkland JL, Ma J, Guo W.
Department of Medicine, Obesity Research Center, Boston University
School of Medicine, Boston, MA 02118, USA. Published in: Metabolism.
2007 Jul;56(7):985-91.
Prior studies of medium-chain triglyceride (MCT) suggest that MCT
might be a useful tool for body fat mass management in obese
nondiabetic humans. We now report a pilot study that tests if MCT is
beneficial for moderately overweight subjects with type 2 diabetes
mellitus. The study was conducted in a group of 40 free-living
subjects in an urban area of China. The subjects were randomized
into 2 test groups, with one given MCT and the other corn oil as
control for long-chain triglycerides (LCTs). The test oil (18 g/d)
was administered as part of daily food intake for 90 days. All
subjects completed the study with self-reported full compliance.
Body weight, waist circumference (WC), and serum samples were
analyzed on days 0, 45, and 90. The MCT group showed an across-time
reduction in body weight and WC, an increase in serum C-peptide
concentration, a reduction in homeostasis model assessment of
insulin resistance, and a decrease in serum cholesterol
concentration (P < .05, repeated measures). No significant
across-time difference for the above parameters was detected for the
LCT group. These changes were associated with an involuntary
reduction in energy intake in the MCT group (P < .05, repeated
measures). A between-group comparison also shows reduced body
weight, WC, and homeostasis model assessment of insulin resistance
in the MCT group compared with the LCT group at the end of the
study. Collectively, our results suggest a link between moderate
consumption of MCT and improved risk factors in moderately
overweight humans in a low-cost, free-living setting.
2. MARCH 2006: Phytosterols mixed with medium-chain triglycerides
and high-oleic canola oil decrease plasma lipids in overweight men.
Authored by: Rudkowska I, Roynette CE, Nakhasi DK, Jones PJ. School
of Dietetics and Human Nutrition, Faculty of Agricultural and
Environmental Sciences, McGill University, Montreal, Québec, Canada
H9X 3V9. Published in: Metabolism. 2006 Mar;55(3):391-5.
Phytosterols (PSs) have been recently added to various mediums.
Nevertheless, matrices with functional properties, such as
medium-chain triglycerides (MCTs), should be precisely examined for
supplementary advantages. The objective of this study was to
identify the existence of combined biological actions of a
functional oil enriched in PSs within MCTs and high-oleic canola
(HOC), relative to a control (olive oil), in overweight,
hyperlipidemic men using a rigorously controlled dietary
intervention. Twenty-three overweight, hyperlipidemic men consumed
both types of oil in a randomized, crossover trial for 6 weeks each.
Fasted plasma samples were collected on the first and last 2 days of
each study period. Body weight decreased -1.22 +/- 0.35 kg (P =
.0019) and -1.68 +/- 0.47 kg (P = .0016) after the 6-week study
period in the olive oil and functional oil groups, respectively. The
end points for total cholesterol and low-density lipoprotein
cholesterol (LDL-C) in the functional oil group (P = .0006) were
lower than in the olive oil group (P = .0002). Total cholesterol
values decreased from comparable baseline to end point of 4.71 +/-
0.16 mmol/L (P < .0001) in the functional oil phase and 5.14 +/-
0.19 mmol/L (P = .0001) in the olive oil phase (P = .0592). In
addition, LDL-C demonstrated a similar drop, to an end point of 3.12
+/- 0.16 mmol/L (P < .0001) and 3.54 +/- 0.18 mmol/L (P = .0002),
for the functional oil and olive oil groups, respectively, with
significant changes (P = .0221). High-density lipoprotein
cholesterol levels did not change in either treatment.
Triacylglycerol end points decreased in functional oil and olive oil
groups (P = .0195 and .0105, respectively) to the same extent from
baseline. Results indicate that PSs mixed within an MCT- and
HOC-rich matrix lower plasma LDL-C, without significantly changing
the high-density lipoprotein cholesterol concentrations, in
hyperlipidemic, overweight men, and may therefore decrease the risk
of cardiovascular events.
3. FEBRUARY 2006: Metabolic effects of intravenous LCT or MCT/LCT
lipid emulsions in preterm infants. Authored by: Lehner F,
Demmelmair H, Röschinger W, Decsi T, Szász M, Adamovich K, Arnecke
R, Koletzko B. Dr. von Hauner Children's Hospital, Ludwig-Maximilians-University,
Munich, Germany. Published in: J Lipid Res. 2006 Feb;47(2):404-11.
Epub 2005 Nov 18.
Most lipid emulsions for parenteral feeding of premature infants are
based on long-chain triacylglycerols (LCTs), but inclusion of
medium-chain triacylglycerols (MCTs) might provide a more readily
oxidizable energy source. The influence of these emulsions on fatty
acid composition and metabolism was studied in 12 premature
neonates, who were randomly assigned to an LCT emulsion (control) or
an emulsion with a mixture of MCT and LCT (1:1). On study day 7, all
infants received [13C]linoleic (LA) and [13C]alpha-linolenic acid
(ALA) tracers orally. Plasma phospholipid (PL) and triacylglycerol
(TG) fatty acid composition and 13C enrichments of plasma PL fatty
acids were determined on day 8. After 8 days of lipid infusion,
plasma TGs in the MCT/LCT group had higher contents of C8:0 (0.50
+/- 0.60% vs. 0.10 +/- 0.12%; means +/- SD) and C10:0 (0.66 +/-
0.51% vs. 0.15 +/- 0.17%) than controls. LA content of plasma PLs
was slightly lower in the MCT/LCT group (16.47 +/- 1.16% vs. 18.57
+/- 2.09%), whereas long-chain polyunsaturated derivatives (LC-PUFAs)
of LA and ALA tended to be higher. The tracer distributions between
precursors and products (LC-PUFAs) were not significantly different
between groups. Both lipid emulsions achieve similar plasma
essential fatty acid (EFA) contents and similar proportional
conversion of EFAs to LC-PUFAs. The MCT/LCT emulsion seems to
protect EFAs and LC-PUFAs from beta-oxidation.
4. JULY 2005: Impairment of VLDL secretion by medium-chain fatty
acids in chicken primary hepatocytes is affected by the chain
length. Authored by: Sato K, Cho Y, Tachibana S, Chiba T, Schneider
WJ, Akiba Y. Laboratory of Animal Nutrition, Graduate School of
Agricultural Science, Tohoku University, Japan.kan@bios.tohoku.ac.jp.
Published in: J Nutr. 2005 Jul;135(7):1636-41.
To determine the effect of the chain length of medium-chain fatty
acids (MCFAs) on VLDL secretion, the media of chicken hepatocyte
cultures were supplemented with hexanoate (6:0), octanoate (8:0),
decanoate (10:0), or dodecanoate (12:0). The supplementation of
palmitate (16:0) or bovine serum albumin (BSA) alone in media was
used as the positive control or the control, respectively. Palmitate
significantly increased intracellular triacylglycerol (TG)
accumulation and VLDL-TG, -cholesterol, and -apolipoprotein (apo)B
secretion. On the other hand, the addition of hexanoate did not
affect these variables relative to control cultures supplemented
with BSA alone, whereas octanoate, decanoate, and dodecanoate
decreased apoB secretion from the chicken hepatocytes. ApoB
secretion from hepatocytes cultured with 1.0 mmol/L MCFA, in
particular decanoate and dodecanoate, in the presence of 0.2 mmol/L
palmitate was significantly lower than that obtained with 0.2 mmol/L
palmitate alone. Decanoate at 0.25-1.0 mmol/L dose dependently
reduced apoB mRNA expression compared with the control (BSA alone).
The levels of 3-hydroxy-3-metylglutaryl-CoA reductase and apoA-I
mRNA were significantly lower in cultures supplemented with
hexanoate, octanoate, and decanoate than in cultures with
dodecanoate and palmitate. These changes did not correspond to the
reduction in VLDL-apoB secretion. We suggest that MCFAs with
different chain lengths differentially affect apoB secretion and
mRNA expression, with decanoate being the most effective at
decreasing VLDL-apoB secretion by regulating apoB mRNA expression at
the transcriptional level.
5. FEBRUARY 2005: A comparison of the effect of medium- vs.
long-chain triglycerides on the in vitro solubilization of
cholesterol and/or phytosterol into mixed micelles. Authored by: von
Bonsdorff-Nikander A, Christiansen L, Huikko L, Lampi AM, Piironen
V, Yliruusi J, Kaukonen AM. Faculty of Pharmacy, University of
Helsinki, Finland. anna.vonbonsdorff@helsinki.fi. Published in:
Lipids. 2005 Feb;40(2):181-90.
Despite clinical evidence of the cholesterol-lowering effects of
phytosterols, the exact mechanisms involved are still unclear.
Displacement of cholesterol by phytosterols from mixed micelles,
which is due to their greater hydrophobicity, is one of the
hypotheses for the lumenal effects contributing to the reduction of
intestinal cholesterol absorption. In this study a dynamic in vitro
lipolysis method was used to examine the solubilization behavior of
cholesterol and/or phytosterols during lipolysis to probe the
efficacy of cholesterol displacement from mixed micelles by
phytosterols. The effects of lipid chain length on sterol
solubilization were studied by using microcrystalline suspensions
containing 17% phytosterol or cholesterol, formulated in long-chain
TG (LCT) and medium-chain TG (MCT). When digesting
cholesterol-suspended in LCT, the entire cholesterol dose was
incorporated into the micellar phase. For the cholesterol
formulation suspended in MCT, 50.3% of the initial dose was
recovered in the micelles. Under the respective conditions, we
observed lower solubilization of phytosterols than of cholesterol
(roughly fourfold). Only 25% of the initial phytosterol dose was
solubilized from suspensions formulated with LCT, and 13% was
solubilized from MCT formulations. Co-administration of phytosterol
and cholesterol suspensions showed a significant reduction of
cholesterol solubilization, particularly when dosed in MCT, with
approximately 25% of the cholesterol dose solubilized. Insignificant
amounts of cholesterol were displaced by phytosterols when
cholesterol was presolubilized in the mixed micelles. The results
show that, compared with LCT, mixed micelles containing MCT
lipolysis products have a reduced solubilizing capacity for
cholesterol, which adds to the effectiveness of the phytosterols in
displacing cholesterol. This suggests potential benefits of using
medium chain length lipids in cholesterol-lowering phytosterol
products.
6. SEPTEMBER 2003: Effects of highly purified structured lipids
containing medium-chain fatty acids and linoleic acid on lipid
profiles in rats. Authored by: Nagata J, Kasai M, Watanabe S, Ikeda
I, Saito M. Division of Food Science, Incorporated Administrative
Agency, National Institute of Health and Nutrition, Tokyo, Japan.
jnagata@nih.go.jp. Published in: Biosci Biotechnol Biochem. 2003
Sep;67(9):1937-43.
The purpose of this study is to examine the effects of highly
purified structured lipids on serum and liver lipid profiles in
rats. We also investigated in vitro hydrolysis of lipid emulsions by
porcine pancreas. Hydrolysis rates of medium chain (M)-linoleic
(L)-medium chain (M) types were 2 to 3 times higher than those of
L-M-L types. The diet containing structured lipids or corn oil was
administered to rats for 4 weeks. There were no significant
differences in growth and food efficiency. Serum cholesterol levels
were significantly lower (P<0.05) in the
2-octanoyl-1,3-dilinoleoyl-glycerol,
2-linoleoyl-1,3-didecanoyl-glycerol, and
2-decanoyl-1,3-dilinoleoyl-glycerol groups than in the corn-oil
group. Serum triglyceride levels were significantly lower (P<0.05)
in rats fed L-M-L types than those in the other groups. Serum non-esterified
fatty acid (NEFA) and beta-hydroxybutylate levels were significantly
higher (P<0.01) in rats fed M-L-M types than those of the other
groups. These results indicate that the feeding of highly purified
L-M-L types could effectively improve serum and liver lipid profiles
and that M-L-M types may be a preferable substrate for the pancreas
and contribute to energy supply in rats.
7. JUNE 2003: Consumption of a functional oil rich in phytosterols
and medium-chain triglyceride oil improves plasma lipid profiles in
men. Authored by: St-Onge MP, Lamarche B, Mauger JF, Jones PJ.
School of Dietetics and Human Nutrition, McGill University,
Ste-Anne-de-Bellevue, Québec, Canada, H9X 3V9. Published in: J Nutr.
2003 Jun;133(6):1815-20.
Medium-chain triglycerides (MCT) have been proposed as
weight-lowering agents, although there is some concern regarding
their hyperlipidemic effect. This study evaluates the effects of a
combination of MCT oil, phytosterols and flaxseed oil [functional
oil (FctO)] on plasma lipid concentrations and LDL particle size.
Twenty-four healthy overweight men (body mass index 28.2 +/- 0.4
kg/m(2)) consumed controlled diets designed to maintain weight for
two periods of 29 d each. Diets contained 40% of energy as fat, 75%
of which was added fat, either FctO or olive oil (OL). Body
composition and blood samples were analyzed at the baseline and the
endpoint of each period. Total cholesterol concentration decreased
12.5% (-0.68 mmol/L; P < 0.05) when subjects consumed FctO and 4.7%
when they consumed OL. Similarly, FctO consumption lowered LDL
cholesterol concentrations by 13.9%, whereas OL consumption did not.
There was no difference in absolute change in LDL-cholesterol
between FctO and OL consumption. Peak LDL particle size was greater
in those who consumed FctO than in those who consumed OL (P < 0.05),
with no effect of diet on proportion of large, medium or small
particles. We conclude that those who consume a diet containing FctO
have a better lipid profile than those who consume a diet rich in OL,
which also leads to a larger lipoprotein particle size. Functional
oil consumption can therefore help reduce the risk of cardiovascular
disease.
8. JUNE 2003: Consumption of an oil composed of medium chain
triacyglycerols, phytosterols, and N-3 fatty acids improves
cardiovascular risk profile in overweight women. Authored by:
Bourque C, St-Onge MP, Papamandjaris AA, Cohn JS, Jones PJ. School
of Dietetics and Human Nutrition, McGill University,
Ste-Anne-de-Bellevue, Quebec, Canada. Published in: Metabolism. 2003
Jun;52(6):771-7.
Medium chain triacylglycerols (MCT) have been suggested as
efficacious in weight management because they possess greater
thermogenic qualities relative to long chain triacylglycerols;
however, MCT may also increase circulating lipid concentrations,
possibly increasing risk of cardiovascular disease (CVD). The
present objective was to examine the effect of a diet supplemented
with a functional oil (FctO) composed of energy
expenditure-enhancing MCT (50% of fat), cholesterol-lowering
phytosterols (22 mg/kg body weight), and triacylglycerol-suppressing
n-3 fatty acids (5% of fat), versus a beef tallow-based diet (BT),
on plasma lipid and aminothiol concentrations. In a randomized,
single-blind, crossover design, partially-inpatient trial, 17
overweight women consumed each oil as part of a controlled,
supervised, targeted energy balance diet for 27 days, with 4 or 8
weeks of washout between phases. Mean plasma total cholesterol
concentration was lower (P <.0001), by 9.1%, on FctO (4.37 +/- 0.20
mmol/L) versus BT (4.80 +/- 0.20 mmol/L). Mean plasma low-density
lipoprotein (LDL) cholesterol was also lower (P <.0001) following
FctO (2.39 +/- 0.15 mmol/L) versus BT (2.86 +/- 0.16 mmol/L),
representing a 16.0% difference between diets. High-density
lipoprotein (HDL) cholesterol and circulating triacylglycerol
concentrations remained unaffected by treatment. Ratios of HDL:LDL
and HDL:total cholesterol were higher (P <.01) by 22.0% and 11.0%,
respectively, on FctO versus BT. Plasma total homocysteine remained
unchanged with FctO, but decreased (P <.05) with control, hence
higher (P <.05) end points were observed with FctO (6.95 +/- 0.33
micromol/L) versus BT (6.27 +/- 0.28 micromol/L). Plasma glutathione
increased (P <.05) by 0.44 micromol/L with FctO supplementation. In
conclusion, despite equivocal effects on homocysteine levels,
consumption of a functional oil composed of MCT, phytosterols, and
n-3 fatty acids for 27 days improves the overall cardiovascular risk
profile of overweight women.
9. MARCH 2003: Medium-chain triglycerides increase energy
expenditure and decrease adiposity in overweight men. Authored by:
St-Onge MP, Ross R, Parsons WD, Jones PJ. School of Dietetics and
Human Nutrition, McGill University, Ste-Anne-de-Bellevue, Quebec,
Canada. Published in: Obes Res. 2003 Mar;11(3):395-402.
OBJECTIVE: The objectives of this study were to compare the effects
of diets rich in medium-chain triglycerides (MCTs) or long-chain
triglycerides (LCTs) on body composition, energy expenditure,
substrate oxidation, subjective appetite, and ad libitum energy
intake in overweight men. RESEARCH METHODS AND PROCEDURES:
Twenty-four healthy, overweight men with body mass indexes between
25 and 31 kg/m(2) consumed diets rich in MCT or LCT for 28 days each
in a crossover randomized controlled trial. At baseline and after 4
weeks of each dietary intervention, energy expenditure was measured
using indirect calorimetry, and body composition was analyzed using
magnetic resonance imaging. RESULTS: Upper body adipose tissue (AT)
decreased to a greater extent (p < 0.05) with functional oil (FctO)
compared with olive oil (OL) consumption (-0.67 +/- 0.26 kg and
-0.02 +/- 0.19 kg, respectively). There was a trend toward greater
loss of whole-body subcutaneous AT volume (p = 0.087) with FctO
compared with OL consumption. Average energy expenditure was 0.04
+/- 0.02 kcal/min greater (p < 0.05) on day 2 and 0.03 +/- 0.02
kcal/min (not significant) on day 28 with FctO compared with OL
consumption. Similarly, average fat oxidation was greater (p =
0.052) with FctO compared with OL intake on day 2 but not day 28.
DISCUSSION: Consumption of a diet rich in MCTs results in greater
loss of AT compared with LCTs, perhaps due to increased energy
expenditure and fat oxidation observed with MCT intake. Thus, MCTs
may be considered as agents that aid in the prevention of obesity or
potentially stimulate weight loss.
10. 2003: Effect of dietary medium- and long-chain triacylglycerols
(MLCT) on accumulation of body fat in healthy humans. Authored by:
Kasai M, Nosaka N, Maki H, Negishi S, Aoyama T, Nakamura M, Suzuki
Y, Tsuji H, Uto H, Okazaki M, Kondo K. Division of Healthcare
Science Research Laboratory, Nisshin Oillio LTD., Yokosuka,
Kanagawa, Japan. m-kasai@nisshin.oilliogroup.com. Published in: Asia
Pac J Clin Nutr. 2003;12(2):151-60.
We investigated whether a structured medium- and long-chain
triacylglycerols (MLCT) diet could decrease accumulation of body fat
in healthy humans. The study was conducted under a double-blind
randomized design. Ninety-three subjects participated in this study.
However, 10 subjects could not consume the specified meal, and one
subject wished to opt out. Consequently, the study included 82
subjects. The experimental subjects consumed the test bread, which
was made with 14 g of MLCT containing 1.7 g MCFA, daily at breakfast
during the study period of 12 weeks, and the control subjects
consumed bread made with long-chain triacylglycerols (LCT). All
subjects consumed the same standard packaged meals. Body composition
parameters were body weight, total body fat and abdominal fat, and
blood analyses included serum cholesterol, triacylglycerols and
phospholipids. Significant decreases of body weight, the amount of
body fat, subcutaneous and visceral fat were noted in the MLCT group
as compared with those of the LCT group for 12 weeks (P<0.05).
Furthermore, a significant decrease in serum total cholesterol was
noted in the MLCT group as compared with that of the LCT group at 8
weeks (P<0.05). However, other serum parameters were not different
between the MLCT and LCT groups. The results suggest that the daily
intake of MLCT diet could result in a reduction in body weight and
in accumulation of body fat, and, moreover, it could reduce serum
total cholesterol.
11. NOVEMBER 2001: Dietary medium-chain triacylglycerols suppress
accumulation of body fat in a double-blind, controlled trial in
healthy men and women. Authored by: Tsuji H, Kasai M, Takeuchi H,
Nakamura M, Okazaki M, Kondo K. Division of Healthcare Science
Research Laboratory, Nisshin Oil Mills, Ltd., Kanagawa 239-0832,
Japan. Kagawa Nutrition University, Saitama 350-0288, Japan.
hiroaki.tsuji@nisshin-seiyu.co.jp. Published in: J Nutr. 2001
Nov;131(11):2853-9.
We investigated the effect of long-term ingestion of dietary
medium-chain triacylglycerols (MCT) on body weight and fat in
humans. Using a double-blind, controlled protocol, we assessed the
potential health benefits of MCT compared with long-chain
triacylglycerols (LCT) in 78 healthy men and women [body mass index
(BMI) > or = 23 kg/m(2): n = 26 (MCT), n = 30 (LCT); BMI < 23
kg/m(2): n = 15 (MCT), n = 7 (LCT)]. Changes in anthropometric
variables, body weight and body fat during the 12-wk MCT treatment
period were compared with those in subjects consuming the LCT diet.
The subjects were asked to consume 9218 kJ/d and 60 g/d of total
fat. The energy, fat, protein and carbohydrate intakes did not
differ significantly between the groups. Body weight and body fat in
both groups had decreased by wk 4, 8 and 12 of the study. However,
in the subjects with BMI > or = 23 kg/m(2), the extent of the
decrease in body weight was significantly greater in the MCT group
than in the LCT group. In subjects with BMI > or = 23 kg/m(2), the
loss of body fat in the MCT group (-3.86 +/- 0.3 kg) was
significantly greater than that in the LCT group (-2.75 +/- 0.2 kg)
at 8 wk. In addition, in subjects with BMI > or = 23 kg/m(2), the
decrease in the area of subcutaneous fat in the MCT group was
significantly greater than that in the LCT group at wk 4, 8 and 12.
These results suggest that the MCT diet may reduce body weight and
fat in individuals (BMI > or = 23 kg/m(2)) more than the LCT diet.
12. JANUARY 2003: Effect of medium-chain triglycerides on the
postprandial triglyceride concentration in healthy men. Authored by:
Kasai M, Maki H, Nosaka N, Aoyama T, Ooyama K, Uto H, Okazaki M,
Igarashi O, Kondo K. Division of Healthcare Science Research
Laboratory, Nisshin Oil Mills LTD., 1 Shinmei-cho, Yokosuka,
Kanagawa 239-0832, Japan. m-kasai@nisshin.oilliogroup.com. Published
in: Biosci Biotechnol Biochem. 2003 Jan;67(1):46-53.
This study compared the serum lipid concentrations after a single
dose of medium-chain triglycerides (MCT) or long-chain triglycerides
(LCT) between individuals grouped according to the body mass index
(BMI). Twenty-five males participated as volunteers, the test diet
containing 10 g of MCT or LCT. Blood samples were collected up to 6
h after the intake of a test diets. The LCT diet resulted in
significantly greater increases in areas under the curves (AUCs) for
serum and chylomicron triglyceride in the BMI > or = 23 kg/m2 group
than those in the BMI < 23 kg/m2 group. The magnitude of response
after intake of the MCT diet by the BMI > or = 23 kg/m2 group was
significantly lower than that after the LCT diet. These results
suggest that, in subjects with BMI > or = 23 kg/m2, the intake of
MCT is preferable to that of LCT for maintaining postprandial
triglyceride at a low concentration.
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References
Kaunitz, H., C. A. Slanetz, R. E. Johnson, V. K. Babayan, and G.
Barsky. 1958. Relation of saturated, medium and long-chain
triglycerides to growth, appetite, thirst and weight maintenance
requirements. J. Nutr. 64: 513-524.
Bach, A. C., and V. K. Babayan. 1982. Mediumchain triglycerides: an
update. Am. J. Clin. Nutr. 36 950-962.
Megremis, C. J. 1991. Medium chain triglycerides: a non-conventional
fat. Food Technol. 45: 108-114.
Timmermann, F. 1993. Medium chain triglycerides. The unconventional
oil. Znt. Food Ingredients. 3: 11-18.
Bach, A. C., A. Frey, and 0. Lutz. 1989. Clinical and experimental
effects of medium-chain-triglyceride-basedfat emulsions. A review.
Clin. Nutr. 8: 223-235.
Kaunitz, H. 1978. Clinical uses of medium-chain triglycerides. Drug.
Ther. 16: 91-99.
Geliebter, A., N. Torbay, E. F. Bracco, S. A. Hashim, and T. B. Van
Itallie. 1983. Overfeeding with medium-chain triglyceride diet
results in diminished deposition of fat. Am. J. Clin. Nutr. 37: 1-4.
Geliebter, A., E. F. Bracco, T. B. Van Itallie, and S. A. Hashim.
1984. Medium-chain triglyceride diet and obesity. Int. J. Obes. 8:
191-192.
Ling, P. R., K. J. Hamawy, L. L. Moldawer, N. Istfan, B. R. Bistrian,
and G. L. Blackburn. 1986. Evaluation of the protein quality of
diets containing medium and long chain triglyceride in healthy rats.
J. Nutr. 116: 343-349.
Babayan, V. K. 1989. Medium chain trig1ycerides.J. Am. Oil Chem.
SOC. 66: 73-86.
Yost, T. J., and R. H. Eckel. 1989. Hypocaloric feeding in obese
women: metabolic effects of medium-chaintriglyceride substitution.
Am. J. Clin. Nutr. 49: 326-330.
Hamosh, M., M. L. Spear, J. Bitman, N. R. Mehta, D. L. Wood, and P.
Hamosh. 1991. Medium chain triglycerides: advantages and possible
drawbacks. In Inborn Errors of Metabolism. J. Schaub, F. Van Hoof,
and H. L. Vis, editors. Vevey Raven Press, New York. 81-92. 338-345.
Tantibhedhyangkul, P., S. A. Hashim, and T. B. Van Ittalie. 1967.
Effects of ingestion of long-chain and medium-chain triglycerides on
glucose tolerance in man. Diabetes. 16: 796-799.
Rath, R., I. Skala, and E. Rathova. 1972. Metabolic aspects of the
use of medium chain triglycerides in the treatment of obesity. Z.
Emuhrungswiss. 13: 116-124.
Wilson, D. E., I. F. Chan, K. B. Stevenson, S. C. Horton, and C.
Schipke. 1983. Eucaloric substitution of medium chain triglycerides
for dietary long chain Fatty acids in acquired total lipodystrophy:
effects on hyperlipoproteinemia and endogenous insulin resistance.
J. Clin. Endocrinol. Metab. 57: 517-523.
Eckel, R. H., A. S. Hanson, A. Y. Chen, J. N. Berman, T. J. Yost,
and E. P. Brass. 1992. Dietary substitution of medium-chain
triglycerides improves insulin-mediated glucose metabolism in NIDDM
subjects. Diabetes. 41: 641-647.
Mebane, D., and L. L. Madison. 1964. Hypoglycemic action of ketones.
I. Effects of ketones on hepatic glucose output and peripheral
glucose utilization. J. Lab. Clin. Med. 63: 177-192.
Sanbar, S. S., G. Hetenyi, N. Forbath, and J. R. Evans. 1965.
Effects of infusion of octanoate on glucose concentration in plasma
and the rates of glucose production and utilization in dogs.
Metabolism. 14: 131 1-1323.
Guy, D. G., and R. J. Tuley. 1981. Effect of diets high in
carbohydrate, soy oil, mediumchain triglycerides or tripelargonin on
blood and liver lipid and glucose intermediates in meal-eating rats.
J. Nutr. 111: 1437-1445.
Randle, P. J., A. L. Kerberg, and J. Espinal. 1988. Mechanisms
decreasing glucose oxidation in diabetes and starvation: role of
lipid fuels and hormones. Diabetes Metab. REV. 4: 623-638.
Grossman, S. P. 1975. Role of the hypothalamus in the regulation of
food and water intake. Psychol. Rev. 82: 64 1-647. REV. 4: 623-638.
200-224.
Kovacs EM, Westerterp-Plantenga MS, Saris WH. The effects of 2-week
ingestion of hydroxycitrate and hydroxycitrate combined with
medium-chain triglycerides on satiety, fat oxidation, energy
expenditure and body weight. Int J Obes Relat Metab Disord. 2001
Jul;25(7):1087-94.
Dulloo AG, Fathi M, Mensi N, Girardier L. Twenty-four-hour energy
expenditure and urinary catecholamines of humans consuming
low-to-moderate amounts of medium-chain triglycerides: a
dose-response study in a human respiratory chamber. Eur J Clin Nutr.
1996 Mar;50(3):152-8.
Hainer V, Kunesova M, Stich V, Zak A, Parizkova J. The role of oils
containing triacylglycerols and medium-chain fatty acids in the
dietary treatment of obesity. The effect on resting energy
expenditure and serum lipids. Cas Lek Cesk. 1994 Jun
13;133(12):373-5. Czech.
Dias VC, Fung E, Snyder FF, Carter RJ, Parsons HG. Effects of
medium-chain triglyceride feeding on energy balance in adult humans.
Metabolism. 1990 Sep;39(9):887-91.
Tsuji, H., Kasai, M., Takeuchi, H., Nakamura, M., Okazaki, M. &
Kondo, K. (2001) Dietary medium-chain triacylglycerols suppress
accumulation of body fat in a double-blind, controlled trial in
healthy men and women. J. Nutr. 131:2853-2839.
St-Onge, M.-P., Ross, R., Parsons, W. D. & Jones, P.J.H. (2003)
Consumption of a functional oil containing medium chain
triglycerides by overweight men increases energy. Obes. Res.
11:395-402.
Hashim, S. A. (1967) Medium-chain triglycerides-clinical and
metabolic aspects. J. Am. Diet. Assoc. 51:221-227.
Han, J., Hamilton, J. A., Kirkland, J. L., Corkey, B. E. & Guo, W.
(2003) Dietary medium chain oil reduces adipose tissue mass and down
regulates expression of adipogenic genes in rats. Obes. Res. in
press.
Guo, W., Choi, J. K., Kirkland, J. L., Corkey, B. E. & Hamilton, J.
A. (2000) Esterification of free fatty acids in adipocytes: a
comparison between octanoate and oleate. Biochem. J. 349:463-471.
Clore, J. N., Allred, J., White, D., Li, J. & Stillman, J. (2002)
The role of plasma fatty acid composition in endogenous glucose
production in patients with type 2 diabetes mellitus. Metabolism
51:1471-1477.
Berge, R. K., Madsen, L., Vaagenes, H., Tronstad, K. J., Gottlicher,
M. & Rustan, A. C. (1999) In contrast with docosahexaenoic acid,
eicosapentaenoic acid and hypolipidaemic derivatives decrease
hepatic synthesis and secretion of triacylglycerol by decreased
diacylglycerol acyltransferase activity and stimulation of fatty
acid oxidation. Biochem. J. 343:191-197.
Han, J., Farmer, S. R., Kirkland, J. L., Corkey, B. E., Yoon, R.,
Pirtskhalava, T., Ido, Y. & Guo, W. (2002) Octanoate attenuates
adipogenesis in 3T3-L1 preadipocytes. J. Nutr. 132:904-910.
Soboll, S., Grundel, S., Schwabe, U. & Scholz, R. (1984) Influence
of fatty acids on energy metabolism. 2. Kinetics of changes in
metabolic rates and changes in subcellular adenine nucleotide
contents and pH gradients following addition of octanoate and oleate
in perfused rat liver. Eur. J. Biochem. 141:231-236.
Benthem L, Keizer K, Wiegman CH, de Boer SF, Strubbe JH, Steffens
AB, Kuipers F, Scheurink AJ. Excess portal venous long-chain fatty
acids induce syndrome X via HPA axis and sympathetic activation. Am
J Physiol Endocrinol Metab. 2000 Dec;279(6):E1286-93.
Guo W, Choi JK, Kirkland JL, Corkey BE, Hamilton JA. Esterification
of free fatty acids in adipocytes: a comparison between octanoate
and oleate. "...substitution of octanoate for oleate or other
long-chain fatty acids could have the beneficial effect of
diminishing fat-cell number and lipid content." Biochem J. 2000 Jul
15;349(Pt 2):463-71.
Van Wymelbeke V, Himaya A, Louis-Sylvestre J, Fantino M. Influence
of medium-chain and long-chain triacylglycerols on the control of
food intake in men. Am J Clin Nutr. 1998 Aug;68(2):226-34.
Binnert C, Pachiaudi C, Beylot M, Hans D, Vandermander J, Chantre P,
Riou JP, Laville M. Influence of human obesity on the metabolic fate
of dietary long- and medium-chain triacylglycerols. "... Our
conclusion is that obesity is associated with a defect in the
oxidation of dietary LCTs probably related to an excessive uptake by
the adipose tissue of meal-derived long-chain fatty acids. MCTs, the
oxidation of which is not altered in obesity, could therefore be of
interest in the dietary treatment of obesity." Am J Clin Nutr. 1998
Apr;67(4):595-601.
Van Zyl CG, Lambert EV, Hawley JA, Noakes TD, Dennis SC. Effects of
medium-chain triglyceride ingestion on fuel metabolism and cycling
performance. "...These data suggest that MCT oxidation decreased the
direct and/or indirect (via lactate) oxidation of muscle glycogen. A
reduced reliance on CHO (carbohydrate) oxidation at a given O2
uptake is similar to an endurance-training effect, and that may
explain the improved T-trial performances." J Appl Physiol. 1996
Jun;80(6):2217-25.
Eckel RH, Hanson AS, Chen AY, Berman JN, Yost TJ, Brass EP. Dietary
substitution of medium-chain triglycerides improves insulin-mediated
glucose metabolism in NIDDM subjects. "Thus, MCT-containing diets
increased insulin-mediated glucose metabolism in both diabetic
patients and nondiabetic subjects. In diabetic subjects, this effect
appears to be mediated by increases in insulin-mediated glucose
disposal." Diabetes. 1992 May;41(5):641-7.
Scalfi L, Coltorti A, Contaldo F. Postprandial thermogenesis in lean
and obese subjects after meals supplemented with medium-chain and
long-chain triglycerides. "Our study shows that PPT (post prandial
after meal thermogenesis or metabolism rate) is enhanced in both
lean and obese subjects when LCTs (long-chain triglyceride from
vegetable oils) in a mixed meal are replaced with MCTs (medium-chain
triglycerides from tropical oils like coconut oil)." Am J Clin Nutr.
1991 May;53(5):1130-3.
Bray GA, Lee M, Bray TL. Weight gain of rats fed medium-chain
triglycerides is less than rats fed long-chain triglycerides.
"Weight gain was normal when the diet contained MCT, but was
increased with the higher percentage of corn oil in the diet." Int J
Obes. 1980;4(1):27-32.
Petschow BW, Batema RP, Ford LL. Susceptibility of Helicobacter
pylori to bactericidal properties of medium-chain monoglycerides and
free fatty acids. "Collectively, our data demonstrate that H. pylori
is rapidly inactivated by medium-chain MGs and lauric acid and
exhibits a relatively low frequency of spontaneous development of
resistance to the bactericidal activity of MGs." Antimicrob Agents
Chemother. 1996 Feb;40(2):302-6.
Hornung B, Amtmann E, Sauer G. Lauric acid inhibits the maturation
of vesicular stomatitis virus. J Gen Virol. 1994 Feb;75 ( Pt
2):353-61.
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