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Intestinal dopaminergic activity in obese and lean zucker rats: Response to high salt intake

Title
Intestinal dopaminergic activity in obese and lean zucker rats: Response to high salt intake
Type
Article in International Scientific Journal
Year
2002
Authors
Lucas Teixeira, VA
(Author)
Other
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Hussain, T
(Author)
Other
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Maria Paula Serrão
(Author)
FMUP
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soares-da-silva, p
(Author)
FMUP
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Lokhandwala, MF
(Author)
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Journal
Vol. 24
Pages: 383-396
ISSN: 1064-1963
Publisher: Taylor & Francis
Other information
Authenticus ID: P-000-NS6
Abstract (EN): The present study examined intestinal dopaminergic activity and its response to high salt (HS, 1% NaCl over a period of 24 hours) intake in obese (OZR) and lean Zucker rats (LZR). The basal Na+,K+-ATPase activity (nmol Pi/mg protein/min) in the jejunum of OZR was higher than in LZR on normal salt (NS) (OZR-NS = 111.3 +/- 6.0 vs. LZR-NS = 88.0 +/- 8.3). With the increase in salt intake, the basal Na+,K+-ATPase activity significantly increased in both animals (OZR-HS=145.9 +/- 11.8; LZR-HS=108.8 +/- 6.7). SKF 38393 (10 nM), a specific D-1-like dopamine receptor agonist, inhibited the jejunal Na+,K+-ATPase activity in OZR on HS intake, but failed to inhibit enzyme activity in OZR on NS intake and LZR on NS and HS intakes. The aromatic L-amino acid decarboxylase (AADC) activity in OZR was lower than in LZR on NS intake. The HS intake increased AADC activity in OZR, but not in LZR. During the NS intake the jejunal monoamine oxidase (MAO) activity in OZR was similar to that in LZR. The HS intake significantly decreased MAO activity in both OZR and LZR. The jejunal COMT activity in OZR was higher than in LZR on NS intake. The HS intake reduced COMT activity in OZR but not LZR. It is concluded that inhibition of jejunal Na+,K+-ATPase activity through D, dopamine receptors is dependent on salt intake in OZR, whereas in LZR, the enzyme failed to respond to the activation of D, dopamine receptors irrespective of their salt intake.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 14
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