Up-regulation of Neuropeptide Y Receptors in the Hypothalamus of Monosodium Glutamate-lesioned Sprague-Dawley Rats

2004 ◽  
Vol 7 (4) ◽  
pp. 241-245 ◽  
Author(s):  
A. Stricker-Krongrad ◽  
B. Beck
1991 ◽  
Vol 203 (2) ◽  
pp. 165-171 ◽  
Author(s):  
Agnes Modin ◽  
John Pernow ◽  
Jan M. Lundberg

2010 ◽  
Vol 103 (3) ◽  
pp. 1337-1349 ◽  
Author(s):  
Vijay Lyall ◽  
Tam-Hao T. Phan ◽  
ZuoJun Ren ◽  
Shobha Mummalaneni ◽  
Pamela Melone ◽  
...  

Regulation of the putative amiloride and benzamil (Bz)-insensitive TRPV1t salt taste receptor by phosphatidylinositol 4,5-bisphosphate (PIP2) was studied by monitoring chorda tympani (CT) taste nerve responses to 0.1 M NaCl solutions containing Bz (5 × 10−6 M; a specific ENaC blocker) and resiniferatoxin (RTX; 0–10 × 10−6 M; a specific TRPV1 agonist) in Sprague-Dawley rats and in wildtype (WT) and TRPV1 knockout (KO) mice. In rats and WT mice, RTX elicited a biphasic effect on the NaCl + Bz CT response, increasing the CT response between 0.25 × 10−6 and 1 × 10−6 M. At concentrations >1 × 10−6 M, RTX inhibited the CT response. An increase in PIP2 by topical lingual application of U73122 (a phospholipase C blocker) or diC8-PIP2 (a short chain synthetic PIP2) inhibited the control NaCl + Bz CT response and decreased its sensitivity to RTX. A decrease in PIP2 by topical lingual application of phenylarsine oxide (a phosphoinositide 4 kinase blocker) enhanced the control NaCl + Bz CT response, increased its sensitivity to RTX stimulation, and inhibited the desensitization of the CT response at RTX concentrations >1 × 10−6 M. The ENaC-dependent NaCl CT responses were not altered by changes in PIP2. An increase in PIP2 enhanced CT responses to sweet (0.3 M sucrose) and bitter (0.01 M quinine) stimuli. RTX produced the same increase in the Bz-insensitive Na+response when present in salt solutions containing 0.1 M NaCl + Bz, 0.1 M monosodium glutamate + Bz, 0.1 M NaCl + Bz + 0.005 M SC45647, or 0.1 M NaCl + Bz + 0.01 M quinine. No effect of RTX was observed on CT responses in WT mice and rats in the presence of the TRPV1 blocker N-(3-methoxyphenyl)-4-chlorocinnamide (1 × 10−6 M) or in TRPV1 KO mice. We conclude that PIP2 is a common intracellular effector for sweet, bitter, umami, and TRPV1t-dependent salt taste, although in the last case, PIP2 seems to directly regulate the taste receptor protein itself, i.e., the TRPV1 ion channel or its taste receptor variant, TRPV1t.


1990 ◽  
Vol 611 (1 Central and P) ◽  
pp. 58-72 ◽  
Author(s):  
RÉMI QUIRION ◽  
JEAN-CLAUDE MARTEL ◽  
YVAN DUMONT ◽  
ALAIN CADIEUX ◽  
FRANCOIS JOLICOEUR ◽  
...  

2001 ◽  
Vol 307 (2) ◽  
pp. 113-116 ◽  
Author(s):  
Ee-Hwa Kim ◽  
Younhee Kim ◽  
Mi-Hyun Jang ◽  
Baek-Vin Lim ◽  
Youn-Jung Kim ◽  
...  

1987 ◽  
Vol 74 (2) ◽  
pp. 237-242 ◽  
Author(s):  
Anita Westlind-Danielsson ◽  
Anders Undén ◽  
Janis Abens ◽  
Siv Andell ◽  
Tamas Bartfai

Peptides ◽  
1992 ◽  
pp. 152-153
Author(s):  
J. J. Leban ◽  
D. Heyer ◽  
J. Matthews ◽  
A. J. Daniels

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