Literature DB >> 23710594

Differential sensitivity of Pak5, Pak6, and Pak5/Pak6 double-knockout mice to the stimulant effects of amphetamine and exercise-induced alterations in body weight.

Melody A Furnari, Michelle L Jobes, Tanya Nekrasova, Audrey Minden, George C Wagner.   

Abstract

OBJECTIVES: PAK5 and PAK6 are protein kinases highly expressed in the brain. Previously, we observed that Pak6 knockout mice gained significantly more weight during development than Pak5 knockout mice as well as wild-type controls and double-knockout mice lacking both Pak5 and Pak6. In this study, we assessed the effects of exercise on food intake and weight gain of these mice as well as their sensitivity to the stimulant effects of amphetamine.
METHODS: Mice of each genotype were placed in cages with free access to run wheel exercise or in cages without run wheels for a total of 74 days. Food and fluid intake as well as body weight of each mouse were measured on a weekly basis. Finally, mice were given a high dose of amphetamine and activity levels were observed immediately thereafter for 90 minutes. Brains and testes of mice were assayed for protein levels of the estrogen alpha and progesterone receptors.
RESULTS: While run wheel mice consumed significantly more food, they weighed less than non-run wheel mice. In addition, although Pak6 knockout mice consumed the same amount of food as wild-type mice, they were significantly heavier regardless of run wheel condition. Pak5 knockout mice were found to be more active than other genotypes after amphetamine treatment. Finally, protein levels of the progesterone and estrogen alpha receptors were altered in brain and testes of the Pak6 knockout mice. DISCUSSION: Collectively, these data suggest that PAK6 play a role in weight gain unrelated to exercise and caloric intake and that Pak5 knockout mice are more sensitive to the stimulant effects of amphetamine.

Entities:  

Keywords:  Amphetamine; Body Weight; Exercise; PAK; Run wheel

Mesh:

Substances:

Year:  2013        PMID: 23710594      PMCID: PMC4365912          DOI: 10.1179/1476830513Y.0000000072

Source DB:  PubMed          Journal:  Nutr Neurosci        ISSN: 1028-415X            Impact factor:   4.994


  21 in total

Review 1.  p21-activated protein kinase: a crucial component of morphological signaling?

Authors:  R H Daniels; G M Bokoch
Journal:  Trends Biochem Sci       Date:  1999-09       Impact factor: 13.807

2.  PAK4 kinase is essential for embryonic viability and for proper neuronal development.

Authors:  Jian Qu; Xiaofan Li; Bennet G Novitch; Ye Zheng; Matthew Kohn; Jian-Ming Xie; Spencer Kozinn; Roderick Bronson; Amer A Beg; Audrey Minden
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

3.  Targeted disruption of the gene for the PAK5 kinase in mice.

Authors:  Xiaofan Li; Audrey Minden
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

4.  The CAG repeat polymorphism in the androgen receptor gene modulates body fat mass and serum concentrations of leptin and insulin in men.

Authors:  M Zitzmann; J Gromoll; A von Eckardstein; E Nieschlag
Journal:  Diabetologia       Date:  2002-12-20       Impact factor: 10.122

5.  Stimulatory effect of oral administration of green tea and caffeine on locomotor activity in SKH-1 mice.

Authors:  Laura Michna; Yao-Ping Lu; You-Rong Lou; George C Wagner; Allan H Conney
Journal:  Life Sci       Date:  2003-08-01       Impact factor: 5.037

6.  Voluntary exercise and tail shock have differential effects on amphetamine-induced dopaminergic toxicity in adult BALB/c mice.

Authors:  Kirsten M Carlson; George C Wagner
Journal:  Behav Pharmacol       Date:  2006-09       Impact factor: 2.293

7.  Emerging from the Pak: the p21-activated protein kinase family.

Authors:  M A Sells; J Chernoff
Journal:  Trends Cell Biol       Date:  1997-04       Impact factor: 20.808

8.  Androgen receptor null male mice develop late-onset obesity caused by decreased energy expenditure and lipolytic activity but show normal insulin sensitivity with high adiponectin secretion.

Authors:  WuQiang Fan; Toshihiko Yanase; Masatoshi Nomura; Taijiro Okabe; Kiminobu Goto; Takashi Sato; Hirotaka Kawano; Shigeaki Kato; Hajime Nawata
Journal:  Diabetes       Date:  2005-04       Impact factor: 9.461

9.  Targeted disruption of the Pak5 and Pak6 genes in mice leads to deficits in learning and locomotion.

Authors:  Tanya Nekrasova; Michelle L Jobes; Jenhao H Ting; George C Wagner; Audrey Minden
Journal:  Dev Biol       Date:  2008-07-16       Impact factor: 3.582

Review 10.  Current research on methamphetamine-induced neurotoxicity: animal models of monoamine disruption.

Authors:  Taizo Kita; George C Wagner; Toshikatsu Nakashima
Journal:  J Pharmacol Sci       Date:  2003-07       Impact factor: 3.337

View more
  2 in total

1.  Normal mammary gland development after MMTV-Cre mediated conditional PAK4 gene depletion.

Authors:  Parisa Rabieifar; Ting Zhuang; Tânia D F Costa; Miao Zhao; Staffan Strömblad
Journal:  Sci Rep       Date:  2019-10-08       Impact factor: 4.379

2.  Pdx1-Cre-driven conditional gene depletion suggests PAK4 as dispensable for mouse pancreas development.

Authors:  Miao Zhao; Parisa Rabieifar; Tânia D F Costa; Ting Zhuang; Audrey Minden; Matthias Löhr; Rainer Heuchel; Staffan Strömblad
Journal:  Sci Rep       Date:  2017-08-01       Impact factor: 4.379

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.