1993
DOI: 10.1016/s0022-2275(20)37695-1
|View full text |Cite
|
Sign up to set email alerts
|

Fat cell adrenergic receptors and the control of white and brown fat cell function

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

3
79
0
4

Year Published

1999
1999
2021
2021

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 565 publications
(86 citation statements)
references
References 253 publications
3
79
0
4
Order By: Relevance
“…These results lend further support to the hypothesis that the sympathetic drive to WAT selectively increases during fasting. As shown by immunohistochemical analysis, such an increase involves both parenchymal nerves, from which the spillover of noradrenaline likely causes adipocyte lipolysis via adrenergic receptors (Lafontan and Berlan 1993) and blood vessel nerves.…”
Section: Discussionmentioning
confidence: 97%
“…These results lend further support to the hypothesis that the sympathetic drive to WAT selectively increases during fasting. As shown by immunohistochemical analysis, such an increase involves both parenchymal nerves, from which the spillover of noradrenaline likely causes adipocyte lipolysis via adrenergic receptors (Lafontan and Berlan 1993) and blood vessel nerves.…”
Section: Discussionmentioning
confidence: 97%
“…BAT thermogenesis is a neurally controlled process. Norepinephrine, released by parenchymal sympathetic nerves (Norman et al 1988), interacts with noradrenergic receptors located on the cell membrane of brown adipocytes and induces expression and functional activation of uncoupling protein 1 (UCP1) (Lafontan and Berlan 1993). A member of the mitochondrial inner membrane carrier family, UCP1 uncouples oxidative phosphorylation (Klingenberg and Huang 1999).…”
mentioning
confidence: 99%
“…β 3 -ARs have been mostly studied in adipose cells to increase cAMP levels, activation of lipase, and thermogenesis [ 330 , 331 ]. Most studies suggest that the β 3 -AR produces a negative inotropy in opposition to positive inotropy regulated by the β 1 - or β 2 -AR [ 14 , 16 ], is cardioprotective [ 59 ], and upregulated during human HF [ 60 , 332 ].…”
Section: Ars In Cardiac Metabolism and As Potential Therapeuticsmentioning
confidence: 99%