國立虎尾科技大學 |

Time-Restricted Feeding Attenuates Obesity-Induced Muscle Dysfunction Through Energy Metabolism and Microbiota Modulation.

紀錄類型:	書目-語言資料,手稿 : Monograph/item
正題名/作者:	Time-Restricted Feeding Attenuates Obesity-Induced Muscle Dysfunction Through Energy Metabolism and Microbiota Modulation./
作者:	Livelo, Christopher.
面頁冊數:	1 online resource (170 pages)
附註:	Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
Contained By:	Dissertations Abstracts International85-06B.
標題:	Biomedical engineering. -
電子資源:	click for full text (PQDT)
ISBN:	9798381187809

Time-Restricted Feeding Attenuates Obesity-Induced Muscle Dysfunction Through Energy Metabolism and Microbiota Modulation.
Livelo, Christopher.

Time-Restricted Feeding Attenuates Obesity-Induced Muscle Dysfunction Through Energy Metabolism and Microbiota Modulation. - 1 online resource (170 pages)

Source: Dissertations Abstracts International, Volume: 85-06, Section: B.

Thesis (Ph.D.)--The University of Alabama at Birmingham, 2023.

Includes bibliographical references

Obesity is a global epidemic that affects countless numbers of people caused by genetic and environmental factors including circadian disruption, which poses significant health risks to skeletal muscle physiology and other tissues. While a feeding fasting intervention known as time-restricted feeding (TRF) has been shown to mitigate obesity-related muscle dysfunction, the underlying mechanisms remain a subject of investigation. In this study, we delve into potential mechanisms underlying TRF's protective effects on muscle physiology in the context of diet- and genetic-induced obesity using Drosophila models. Our findings reveal that TRF triggers the upregulation of key genes involved in glycine production (Sardh and CG5955) and utilization (Gnmt). Muscle-specific knockdown of Gnmt, Sardh, and CG5955 resulted in muscle dysfunction, ectopic lipid accumulation, and the loss of TRF-mediated benefits. Furthermore, our investigations unveiled distinct pathways affected by TRF under different obesogenic challenges. While TRF was found to enhance the purine cycle in diet-induced obesity (HFD), TRF activated AMPK and downstream signaling predominantly in genetic-induced obesity.Additionally the microbiome, which is sensitive to lifestyle changes like diet and obesity, can also play a role in muscle physiology. We explored TRF's modulation of the microbiome and the consequences of microbiota removal on skeletal muscle physiology in wildtype and obese Drosophila models, highlighting the intricate interplay between diet, microbiota, and muscle physiology. Notably, (axenic) wildtype Drosophila exhibited reduced muscle performance, elevated insulin resistance and glucose levels, ectopic lipid accumulation, and decreased ATP levels compared to their conventional counterpart. Interestingly, in Drosophila obesity models, improved muscle performance, lower glucose levels, and increased ATP levels in axenic conditions was observed. TRF showed changes in the abundances of specific bacterial species, Acetobacter Pasteurianus and Staphylococcus Aureus, which, when supplemented, led to improvement/worsening (respectively) of skeletal muscle physiology.In summary, our study investigates the pleiotropic impacts of TRF benefits on muscle physiology under varying obesogenic challenges. We investigate the intricate relationship between TRF and the microbiome, pathway modulation, and its impacts on skeletal muscle physiology. These findings provide insights into potential targets for obesity treatment and furthers our understanding in regards to TRF modulated attenuation of obese associated phenotypes in muscle.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2024

Mode of access: World Wide Web

ISBN: 9798381187809Subjects--Topical Terms:

588770
Biomedical engineering.
Subjects--Index Terms:

Glycine metabolismIndex Terms--Genre/Form:

554714
Electronic books.

Time-Restricted Feeding Attenuates Obesity-Induced Muscle Dysfunction Through Energy Metabolism and Microbiota Modulation.
LDR:04145ntm a22004217 4500 001 1149399
005 20241015112542.5
006 m o d
007 cr bn ---uuuuu
008 250605s2023 xx obm 000 0 eng d
020 $a 9798381187809
035 $a (MiAaPQ)AAI30811105
035 $a AAI30811105
040 $a MiAaPQ $b eng $c MiAaPQ $d NTU
100 1 $a Livelo, Christopher. $3 1475619
245 1 0 $a Time-Restricted Feeding Attenuates Obesity-Induced Muscle Dysfunction Through Energy Metabolism and Microbiota Modulation.
264 0 $c 2023
300 $a 1 online resource (170 pages)
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
500 $a Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
500 $a Advisor: Melkani, Girish C.;Bailey, Shannon M.
502 $a Thesis (Ph.D.)--The University of Alabama at Birmingham, 2023.
504 $a Includes bibliographical references
520 $a Obesity is a global epidemic that affects countless numbers of people caused by genetic and environmental factors including circadian disruption, which poses significant health risks to skeletal muscle physiology and other tissues. While a feeding fasting intervention known as time-restricted feeding (TRF) has been shown to mitigate obesity-related muscle dysfunction, the underlying mechanisms remain a subject of investigation. In this study, we delve into potential mechanisms underlying TRF's protective effects on muscle physiology in the context of diet- and genetic-induced obesity using Drosophila models. Our findings reveal that TRF triggers the upregulation of key genes involved in glycine production (Sardh and CG5955) and utilization (Gnmt). Muscle-specific knockdown of Gnmt, Sardh, and CG5955 resulted in muscle dysfunction, ectopic lipid accumulation, and the loss of TRF-mediated benefits. Furthermore, our investigations unveiled distinct pathways affected by TRF under different obesogenic challenges. While TRF was found to enhance the purine cycle in diet-induced obesity (HFD), TRF activated AMPK and downstream signaling predominantly in genetic-induced obesity.Additionally the microbiome, which is sensitive to lifestyle changes like diet and obesity, can also play a role in muscle physiology. We explored TRF's modulation of the microbiome and the consequences of microbiota removal on skeletal muscle physiology in wildtype and obese Drosophila models, highlighting the intricate interplay between diet, microbiota, and muscle physiology. Notably, (axenic) wildtype Drosophila exhibited reduced muscle performance, elevated insulin resistance and glucose levels, ectopic lipid accumulation, and decreased ATP levels compared to their conventional counterpart. Interestingly, in Drosophila obesity models, improved muscle performance, lower glucose levels, and increased ATP levels in axenic conditions was observed. TRF showed changes in the abundances of specific bacterial species, Acetobacter Pasteurianus and Staphylococcus Aureus, which, when supplemented, led to improvement/worsening (respectively) of skeletal muscle physiology.In summary, our study investigates the pleiotropic impacts of TRF benefits on muscle physiology under varying obesogenic challenges. We investigate the intricate relationship between TRF and the microbiome, pathway modulation, and its impacts on skeletal muscle physiology. These findings provide insights into potential targets for obesity treatment and furthers our understanding in regards to TRF modulated attenuation of obese associated phenotypes in muscle.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2024
538 $a Mode of access: World Wide Web
650 4 $a Biomedical engineering. $3 588770
650 4 $a Public health. $3 560998
650 4 $a Molecular biology. $3 583443
650 4 $a Physiology. $3 673386
653 $a Glycine metabolism
653 $a Microbiome
653 $a Obesity
653 $a Skeletal muscle physiology
653 $a Obesogenic challenges
653 $a Lipid metabolism
655 7 $a Electronic books. $2 local $3 554714
690 $a 0719
690 $a 0307
690 $a 0541
690 $a 0573
710 2 $a The University of Alabama at Birmingham. $b Pathology. $3 1475520
710 2 $a ProQuest Information and Learning Co. $3 1178819
773 0 $t Dissertations Abstracts International $g 85-06B.
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30811105 $z click for full text (PQDT)