Metabolic parameters of Id1−/− and wild-type mice fed a standard chow diet (hatched bars and striped bars, respectively) or a high-fat diet (black bars.

Slides:



Advertisements
Similar presentations
The FATZO mouse as a Translational Model for the Development of Drugs for Obesity, Metabolic Syndrome and Diabetes. PreClinOmics, Inc. 1.
Advertisements

Supplemental figure 1 Adipocyte SVF E CD AB Supplemental figure 1: Impaired expression of Am2 and Ramps in obese mice (A-E) mRNA levels of Am2, Crlr, Ramp1,
Volume 6, Issue 4, Pages (April 2017)
Role of thyroid hormone homeostasis in obesity-prone and obesity-resistant mice fed a high-fat diet  Shu-Fang Xia, Xiao-Mei Duan, Li-Yue Hao, Li-Ting.
Volume 6, Issue 8, Pages (August 2017)
Volume 5, Issue 10, Pages (October 2016)
Differential effects of angiopoietin-like 4 in brain and muscle on regulation of lipoprotein lipase activity  Sara Gry Vienberg, André Kleinridders, Ryo.
Lecture 14: Two-Way ANOVA
Valsartan Protects Pancreatic Islets and Adipose Tissue From the Inflammatory and Metabolic Consequences of a High-Fat Diet in Mice by Banumathi K. Cole,
Arterioscler Thromb Vasc Biol
Volume 26, Issue 4, Pages e4 (October 2017)
Volume 15, Issue 1, Pages (January 2012)
Volume 16, Issue 10, Pages (September 2016)
CALCULATING THE ATHLETE’S DAILY CALORIC INTAKE
Volume 6, Issue 3, Pages (September 2007)
The adipose tissue of BALB/c scid mice is quantitatively, but not qualitatively, different than that of BALB/c control mice. The adipose tissue of BALB/c.
Volume 16, Issue 7, Pages (August 2016)
Protection against High-Fat-Diet-Induced Obesity in MDM2C305F Mice Due to Reduced p53 Activity and Enhanced Energy Expenditure  Shijie Liu, Tae-Hyung.
Volume 17, Issue 10, Pages (December 2016)
Intra‐eWAT administration of FGF21 vectors in ob/ob mice
Volume 9, Issue 2, Pages (February 2009)
Volume 3, Issue 2, Pages (February 2006)
Volume 14, Issue 5, Pages (November 2011)
Volume 6, Issue 4, Pages (October 2007)
Volume 8, Issue 4, Pages (October 2008)
Volume 9, Issue 1, Pages (January 2009)
Volume 49, Issue 2, Pages (January 2006)
Volume 6, Issue 3, Pages (September 2007)
Volume 16, Issue 3, Pages (July 2016)
Volume 8, Issue 5, Pages (November 2008)
Volume 9, Issue 6, Pages (June 2009)
Mitofusin 2 in Mature Adipocytes Controls Adiposity and Body Weight
PPARγ in Vagal Neurons Regulates High-Fat Diet Induced Thermogenesis
Fig. 6 Transmissibility of adiposity from humanized mice to germ-free recipients. Transmissibility of adiposity from humanized mice to germ-free recipients.
Cellularity of epididymal adipose tissue.
Body weight, blood glucose, and iron status in STZ-induced type 1 diabetic rats with or without insulin therapy. Body weight, blood glucose, and iron status.
Lipin, a lipodystrophy and obesity gene
Chronic brain insulin infusion reduces liver TG content independent of changes in body weight and food intake. Chronic brain insulin infusion reduces liver.
Skeletal muscle characteristics of HFD-induced obese mice.
Dietary regulation of apical GLUT2.
Loss of protection by linagliptin against obesity-related inflammation and insulin resistance in MIP-1α−/− mice. Loss of protection by linagliptin against.
Transgenic restoration of long-chain n-3 PUFA protects against obesity-linked insulin resistance and glucose intolerance. Transgenic restoration of long-chain.
Effect of berberine on white adipose tissue mass.
Reduced β-cell mass in MCH-KO mice on normal chow and high-fat diets.
AgRP-ATF4 KO mice have decreased food intake and enhanced energy expenditure. AgRP-ATF4 KO mice have decreased food intake and enhanced energy expenditure.
Effect of Id1 deletion on insulin action in wild-type and Id1−/− mice fed a chow diet (white triangle/striped bar and black triangle/hatched bar, respectively)
Hepatic fuel metabolism in male 5αR1-KO and WT mice
Mice fed GP-SPI diet show improved fasting glucose and oral glucose tolerance. Mice fed GP-SPI diet show improved fasting glucose and oral glucose tolerance.
Treatment of high-fat diet–fed mice with TTR-ASOs decreases circulating TTR and RBP4 levels, and improves insulin sensitivity. Treatment of high-fat diet–fed.
MϕRIP140KD mice exhibit improved metabolic phenotypes.
Effects of Rosi treatment on ASKO mice.
Effects of chow-diet feeding on control and TRIB3 MOE mice.
Effects of berberine on in vivo metabolism in two animal models of insulin resistance. Effects of berberine on in vivo metabolism in two animal models.
Leucine deprivation increases energy expenditure.
Energy stores in quadriceps muscles at rest (white bars) and after treadmill exercise (black bars) in WT and HSL KO mice. Energy stores in quadriceps muscles.
AP2-Cre–mediated IKKβ deletion results in similar defects in adipose remodeling and accentuated inflammatory responses after HF feeding. aP2-Cre–mediated.
Relative gene expression levels in MIN6 cells.
Metabolic outcomes associated with DIO in E3FAD and E4FAD mice.
High-fat diet–induced glucose intolerance is prevented in ghrelin knockout (Ghr-KO) mice. High-fat diet–induced glucose intolerance is prevented in ghrelin.
β-Cell–specific deletion of Phb2 renders mice diabetic.
Mice lacking Y1 receptor in the hematopoietic compartment remain healthy under normal chow feeding conditions. Mice lacking Y1 receptor in the hematopoietic.
Decreased M1 and increased M2 macrophages in eWAT and liver of DIO mice due to linagliptin administration. Decreased M1 and increased M2 macrophages in.
EPA+DHA supplementation does not alter body composition, body weight, or feed intake. EPA+DHA supplementation does not alter body composition, body weight,
Fig. 4 Effects of hematopoietic restoration of TLR9 on adipose tissue inflammation and insulin resistance. Effects of hematopoietic restoration of TLR9.
Fig. 1. GDF15 is up-regulated with obesity, and AAV-GDF15 improves metabolic parameters in DIO mice. GDF15 is up-regulated with obesity, and AAV-GDF15.
Brown Adipose Tissue Thermogenic Capacity Is Regulated by Elovl6
Volume 26, Issue 1, Pages 1-10.e7 (January 2019)
Volume 6, Issue 6, Pages (December 2007)
Fig. 3. Effects of SFN in mice with diet-induced diabetes.
Volume 4, Issue 4, Pages (October 2006)
Presentation transcript:

Metabolic parameters of Id1−/− and wild-type mice fed a standard chow diet (hatched bars and striped bars, respectively) or a high-fat diet (black bars and white bars, respectively) for 6 weeks. Metabolic parameters of Id1−/− and wild-type mice fed a standard chow diet (hatched bars and striped bars, respectively) or a high-fat diet (black bars and white bars, respectively) for 6 weeks. A: Body weight for wild-type (n = 22) and Id1−/− (n = 22) mice fed a chow diet and wild-type (n = 16) and Id1−/− (n = 11) mice fed a high-fat diet. *P < 0.05 for effect of diet in wild-type and Id1−/− mice. B: Epididymal fat pad weight. Results are expressed as a percentage of body weight for wild-type (n = 5) and Id1−/− (n = 6) mice fed a chow diet and wild-type (n = 7) and Id1−/− (n = 7) mice fed a high-fat diet. **P < 0.01 for effect of diet in wild-type and Id1−/− mice. C: Liver weight for wild-type (n = 10) and Id1−/− (n = 6) mice fed a chow diet and wild-type (n = 8) and Id1−/− (n = 6) mice fed a high-fat diet. D: Energy intake of wild-type (n = 9) and Id1−/− (n = 6) mice fed a chow diet and wild-type (n = 12) and Id1−/− (n = 8) mice fed a high-fat diet. ANOVA: P < 0.05 for effect of diet. Mia C. Åkerfeldt, and D. Ross Laybutt Diabetes 2011;60:2506-2514 ©2011 by American Diabetes Association