The knee cartilage of obese mice who ate the oligofructose supplement was indistinguishable from
that of the lean mice.
Macrophages in the adipose tissue
of lean mice were uniformly small, isolated, and widely dispersed among the adipocytes.
«The nondigestible compounds in the Granny Smith apples actually changed the proportions of fecal bacteria from obese mice to be similar to
that of lean mice,» Noratto said.
Scientists reached this conclusion by transferring microbes from bypass - treated obese mice to a group
of lean mice raised in sterile conditions that left them with no intestinal bacteria at all.
Not exact matches
To find out what was going on in the microbiomes
of four sets
of differently shaped identical twins, researchers transferred some gut bacteria from a
lean (human) twin to a sterile
mouse: one with no foreign bacteria at all.
«How obesity dulls the sense
of taste: Obese
mice had about 25 percent fewer taste buds than
lean mice in study.»
In another animal microbiome experiment, Jeffrey Gordon, a biologist at Washington University in St. Louis, took a suite
of microbes from the guts
of both obese and
lean mice and transplanted them into the guts
of microbe - free
mice.
The
mice that received the microbiomes
of the obese
mice gained significantly more weight than did the
mice with the
lean -
mouse microbiomes.
These
mice lived just as long as semi-starved
lean mice, even though they had at least four times the body fat
of normal
mice.
In the
mice that consumed either type
of tea extract, there was less
of the type
of bacteria associated with obesity and more
of the bacteria associated with
lean body mass.
In this study, he exposed
lean, brown - furred female
mice to 50 milligrams
of BPA per kilogram
of body weight daily, and the next generation was transformed: More
of them were fat, with blond fur.
«Importantly, we found that blocking the actions
of the endocannabinoids with pharmacological inhibitors
of cannabinoid receptors in the periphery completely normalized food intake and meal patterns in western diet - induced obese
mice to levels found in control
lean mice fed standard chow.»
«This is the first study to show that current strategies to bolster the effectiveness
of flu vaccines protected
lean mice from serious illness but fell short
of protecting obese
mice from infections,» said corresponding author Stacey Schultz - Cherry, Ph.D., a member
of the St. Jude Department
of Infectious Diseases.
Separate groups
of germfree
mice were colonized with uncultured fecal microbiota from each member
of four twin pairs discordant for obesity or with culture collections from an obese (Ob) or
lean (Ln) co-twin.
Cohousing
mice harboring an obese twin's microbiota (Ob) with
mice containing the
lean co-twin's microbiota (Ln) prevented the development
of increased body mass and obesity - associated metabolic phenotypes in Ob cage mates.
Moreover, obese - phenotype
mice were invaded by members
of the Bacteroidales from the
lean mice, but, happily, the
lean animals resisted invasion by the obese microbiota.
By comparing the behavior
of XBP - 1s in the obese
mice with that in
lean, healthy ones, he discovered an inflammatory protein that modifies XBP - 1s in healthy animals so it can be shuttled into the nucleus.
Associate Professor Amanda Sainsbury - Salis expressed surprise at the impact
of the Y6 gene deletion on
mice, commenting «I find it amazing that one gene, which is expressed in the small part
of the brain that controls the body clock, has such a profound impact on how much fat is stored on the body, and how much
lean tissue is maintained.»
But the babies
of adiponectin - treated
mice were about the same weight as those born to
lean control
mice, the researchers report online today in the Proceedings
of the National Academy
of Sciences.
Now Catherine Suter at Victor Chang Cardiac Research Institute in Sydney and her colleagues have investigated the longer - term effects
of paternal obesity by mating obese male
mice with
lean females.
To explore that question, a team led by Cornell University biomedical engineer Claudia Fischbach first showed that female
mice that were obese, because
of genetics or a high - fat diet, had more fibrous mammary fat pads with straighter collagen fibers than those seen in
lean mice (see image).
The researchers used electron microscopy and other imaging techniques to view thousands
of cells from the liver tissue
of lean and obese
mice.
Based on the observation that obese
mice, rats, and humans all had elevated serum concentrations
of a protein called GDF15 compared to
lean controls, Yumei Xiong and colleagues set out to develop therapies derived from the molecule.
This is interesting, given that muscle /
lean muscle mass ratios
of non-skeletal muscle organs from IL - 15Rα — KO
mice, such as the heart, spleen, and kidneys, were not significantly different from those
of B6129 controls.
Correlation
of gene expression occurred across
lean and obese
mice, defining a common transcriptional response to variations in adiposity.
Our results indicate that the percentage
of macrophages in the adipose tissue that surrounds and infiltrates the extensor digitalis longus muscle is increased in obese
mice compared with
lean mice.
We examined six experimental groups
of 20 - week - old C57BL / 6J
mice: (a)
lean C57BL / 6J female
mice, (b)
lean C57BL / 6J male
mice, (c) moderately obese C57BL / 6J male
mice with diet - induced obesity, (d) moderately obese female B6.Cg Ay / +
mice, (e) severely obese female B6.V Lepob / ob
mice, and (f) severely obese male B6.V Lepob / ob
mice.
We estimate that the percentage
of macrophages in adipose tissue ranges from under 10 % in
lean mice and humans to over 50 % in extremely obese, leptin - deficient
mice and nearly 40 % in obese humans.
Adipose tissue within muscle contained significant numbers
of F4 / 80 + macrophages, and the percentage
of F4 / 80 + cells within this adipose tissue was markedly increased in obese
mice compared with
lean mice (41 % ± 4 %
of macrophages vs. 12 % ± 2 %
of macrophages, respectively; P < 0.005, mean ± SD)(Figure 4).
Macrophages in the liver and muscle
of lean and obese
mice.
Immunohistochemical detection
of cells expressing the macrophage - specific antigen F4 / 80 (arrows) in extensor digitalis longus muscles from C57BL / 6J (a and c) Lepob / ob female and (b and d)
lean female
mice.
This difference may be explained by the reduced levels
of normal CST in obese
mice compared to the
lean control animals.
We calculated the average adipocyte cross-sectional area and the percentage
of F4 / 80 - expressing cells in the perigonadal, perirenal, mesenteric, and subcutaneous inguinal adipose tissue depots from Ay / + female, Lepob / ob female,
lean male, and diet - induced obese (DIO) male
mice.
Results showing C. minuta has an effect
of controlling fat gain in the
mouse match data that reveal
lean people have a greater abundance
of C. minuta in their gut than obese people.
The percentage
of F4 / 80 - positive macrophages within this adipose tissue was markedly increased in obese compared with
lean mice (e, P < 0.005).
In 2005, together with Washington University microbiologist Jeffrey Gordon and others, Knight used the tools to catalog the microbes that inhabit the intestines
of lean and obese
mice, in hopes
of uncovering relationships between microbes and metabolic health.
Treated
mice become
lean, and develop larger muscles and endurance, suggesting a multitude
of therapeutic uses in people.
While IRAB - A produced a decrease in blood glucose in
lean mice, the data in DIO
mice indicated an exacerbation
of insulin resistance; these data were unexpected and suggested the interplay
of complex unknown pharmacology.
Lean and diet - induced obese
mice were used to characterize single - dose in vivo pharmacological effects
of IRAB - A; multiple - dose IRAB - A effects were tested in obese
mice.
Both obese humans and
mice have significantly elevated soluble Fabp4 / aP2 levels, and injection
of recombinant Fabp4 / aP2 into
lean wild type
mice stimulates hepatic glucose production and gluconeogenesis.
After exercising for six weeks, both obese and
lean mice showed a significant reduction in the overall size
of fat cells and the overall amount fat in the marrow.
In one study, researchers took microbiome samples from both
lean and obese
mice and placed them in the gut
of neutral
mice.
Their procedure involved infecting
mice without microbiota with either microbiota
of obese or
lean mice.
Additionally, fecal transplant
of gut microbes from obese
mice to GF
mice results in greater adiposity in the GF recipients than fecal transplants from
lean donors (2).
Actually, the leucine - deprived
mice showed no difference in
lean mass, from either the control
mice or those that were restricted to the same number
of (reduced) calories consumed by the leucine - deprived
mice.
Pair - fed
mice lost only 5 percent
of bodyweight, and their
lean mass did not change appreciably; leucine deprived
mice lost 15 percent
of body - weight, and their
lean mass was the same as the control
mice, and unchanged.There were no strength or endurance challenges, but when one considers that the
mice lost 50 percent
of abdominal fat, 15 percent
of bodyweight, and had no loss
of lean mass, that is incredible.
However — and this part is miraculous — when Dr. Panda and his team restricted the time the
mice were fed the exact same crappy diet to 12 hours (instead
of allowing them to eat whenever they wanted), none
of the negative health benefits occurred; the Time - Restricted Fed
mice were 70 %
leaner, lived longer and were free from diabetes or heart disease.
To explore whether this was a cause
of obesity or the effect
of it, another research team gave
mice the bacteria from sets
of twins where one was obese and the other was
lean.
This study has examined the effect
of alpha - lipoic acid on glucose uptake by cultured L6 muscle cells and different types
of skeletal muscles in normal
lean (+ / +) and severely insulin - resistant, obese - diabetic (ob / ob)
mice.
A game
of cat and
mouse in the Michigan snow means Mick and her unwelcome cohort must learn to
lean on each other — and that closeness leads to an explosive attraction.