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1.
Biosci Biotechnol Biochem ; 72(9): 2476-80, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18776662

ABSTRACT

The extract of the stem bark of Siberian ginseng, Acanthopanax senticosus Harms (ASH), is believed to play a body-coping role in stress through a brain noradrenergic mechanism. The present study was carried out to investigate the effect of ASH on the neuronal activation patterns of c-Fos expression in the rat brain. With ASH administration, c-Fos accumulated in both the supraoptic nuclei (SON) and paraventricular nuclei (PVN), which regulate stress response. Only the caudal regions in the nucleus of the solitary tract (NTS), a locus innervating both the SON and PVN, were activated. Such a neuro-anatomical pattern associated with ASH suggests the possible involvement of these stress-related brain loci.


Subject(s)
Brain/metabolism , Eleutherococcus/metabolism , Paraventricular Hypothalamic Nucleus/drug effects , Plant Extracts/pharmacology , Solitary Nucleus/metabolism , Supraoptic Nucleus/drug effects , Animals , Eleutherococcus/genetics , Male , Paraventricular Hypothalamic Nucleus/metabolism , Rats , Rats, Sprague-Dawley , Supraoptic Nucleus/metabolism
2.
Neurosci Res ; 57(3): 462-6, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17188385

ABSTRACT

Orexins, recognized for their diverse functions in sleep/wakefulness/arousal and appetite regulation, may play provocative roles in stress response. Although the PVN of the hypothalamus expresses an abundance of orexin-2 receptor (OX-2R), the involvement of OX-2R in regulating ACTH response to stress remains unclear. To address this, we examined effects of a selective antagonist to OX-2R (N-{(1S)-1-[6,7-dimethoxy-3,4-dihydro-2(1H)-isoquinolinyl]carbonyl}-2,2-dimethylpropyl)-N-{4-pyridinylmethyl}amine upon plasma ACTH concentrations after administration of orexin A and swimming stress. Increases in ACTH levels with orexin A or swimming stress were attenuated with prior administration of an OX-2R antagonist. These results suggest that swimming stress facilitates ACTH release, at least in part via activation of OX-2R.


Subject(s)
Adrenocorticotropic Hormone/metabolism , Hypothalamus/metabolism , Intracellular Signaling Peptides and Proteins/metabolism , Neuropeptides/metabolism , Neurosecretory Systems/metabolism , Receptors, G-Protein-Coupled/metabolism , Receptors, Neuropeptide/metabolism , Stress, Psychological/metabolism , Animals , Consciousness/physiology , Hypothalamo-Hypophyseal System/drug effects , Hypothalamo-Hypophyseal System/metabolism , Hypothalamus/drug effects , Male , Neurons/drug effects , Neurons/metabolism , Neurosecretory Systems/drug effects , Orexin Receptors , Orexins , Proto-Oncogene Proteins c-fos/metabolism , Rats , Rats, Wistar , Receptors, G-Protein-Coupled/antagonists & inhibitors , Receptors, Neuropeptide/antagonists & inhibitors , Stress, Psychological/physiopathology , Time Factors
3.
Pflugers Arch ; 453(2): 203-10, 2006 Nov.
Article in English | MEDLINE | ID: mdl-16941139

ABSTRACT

To determine whether IGF-I Ea, MGF, and myostatin mRNAs are related to GH-independent overload-induced muscle growth, we examined the expressions of IGF-I Ea and MGF mRNAs in the plantaris muscle after compensatory overload in hypophysectomized rats. The muscles were divided into four groups: normal-control, normal-overloaded, hypophysectomized-control, and hypophysectomized-overloaded. The weights of the plantaris muscle in the normal-overloaded were significantly higher than those of the normal-control. The weights of the hypophysectomized-overloaded were also significantly higher than those of the hypophysectomized-control. IGF-I Ea and MGF mRNAs in normal-overloaded and hypophysectomized-overloaded 3 days after overload were significantly higher than those of normal-control and hypophysectomized-control, respectively. Myostatin mRNAs in normal-overloaded and hypophysectomized-overloaded 3 days after the overload were significantly lower than those of normal-control and hypophysectomized-control, respectively. Thus, it was shown that IGF-I Ea, MGF, and myostatin mRNAs were expressed in association with muscle enlargement after compensatory overload independently of pituitary state. These observations suggest that the expression of IGF-I Ea, MGF, and myostatin mRNAs due to compensatory overload would be associated in a growth-hormone-independent manner.


Subject(s)
Insulin-Like Growth Factor I/metabolism , Muscle Development/physiology , Muscle, Skeletal/metabolism , Transforming Growth Factor beta/metabolism , Animals , Gene Expression , Hypophysectomy , Male , Myostatin , Rats , Rats, Wistar
4.
Neurosci Lett ; 389(1): 25-9, 2005 Nov 25.
Article in English | MEDLINE | ID: mdl-16055265

ABSTRACT

The potential usefulness of c-fos gene expression as an indicator of the activity level of spinal alpha motoneurons was examined in loaded locomotive rats. The motor pools of the plantaris (PL) and soleus muscles (SOL), mainly composed respectively of fast- and slow-twitch muscle fibers, were investigated in rats under locomotion at 25 m/min on a 20% incline. We first labeled motoneurons with a retrograde tracer, Nuclear Yellow (NY), and then quantified the c-fos mRNA expression level in the NY-labeled alpha motoneurons by means of in situ hybridization. Electromyographic (EMG) activities were also recorded. The c-fos expression level per alpha motoneuron showed a greater increase in the PL (75%) than in the SOL motor pool (38%). EMG activities also showed a greater increase in the PL (159%) than in the SOL (43%). Taken together, these results suggest that c-fos expression levels in alpha motoneurons are associated with the activity levels of their corresponding muscle. This cytochemical method for identifying the c-fos expression level has potential for use as a tool for estimating the activity level of large populations of alpha motoneurons in unrestricted animals.


Subject(s)
Genes, fos , Hindlimb/innervation , Locomotion/physiology , Motor Activity/physiology , Motor Neurons/physiology , Muscle, Skeletal/innervation , Animals , Gene Expression Regulation/physiology , Rats
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