scholarly journals The Contribution of Serotonergic Receptors and Nitric Oxide Systems in the Analgesic Effect of Acetaminophen: An Overview of the Last Decade

2020 ◽  
Vol 17 (1) ◽  
pp. 119-126
Author(s):  
Yeşim HAMURTEKİN ◽  
Ammar NOUILATI ◽  
Cansu DEMİRBATIR ◽  
Emre HAMURTEKİN
1999 ◽  
Vol 127 (4) ◽  
pp. 1039-1047 ◽  
Author(s):  
Daniel Karila-Cohen ◽  
Eric Delpy ◽  
Jean-Luc Dubois-Randé ◽  
Louis Puybasset ◽  
Luc Hittinger ◽  
...  

2011 ◽  
Vol 89 (2) ◽  
pp. 89-95 ◽  
Author(s):  
Ercan Ozdemir ◽  
Ihsan Bagcivan ◽  
Nedim Durmus ◽  
Ahmet Altun ◽  
Sinan Gursoy

Although the phenomenon of opioid tolerance has been widely investigated, neither opioid nor nonopioid mechanisms are completely understood. The aim of the present study was to investigate the role of the nitric oxide (NO)–cyclic guanosine monophosphate (cGMP) pathway in the development of morphine-induced analgesia tolerance. The study was carried out on male Wistar albino rats (weighing 180–210 g; n = 126). To develop morphine tolerance, animals were given morphine (50 mg/kg; s.c.) once daily for 3 days. After the last dose of morphine was injected on day 4, morphine tolerance was evaluated. The analgesic effects of 3-(5′-hydroxymethyl-2′-furyl)-1-benzylindazole (YC-1), BAY 41-2272, S-nitroso-N-acetylpenicillamine (SNAP), NG-nitro-l-arginine methyl ester (L-NAME), and morphine were considered at 15 or 30 min intervals (0, 15, 30, 60, 90, and 120 min) by tail-flick and hot-plate analgesia tests (n = 6 in each study group). The results showed that YC-1 and BAY 41-2272, a NO-independent activator of soluble guanylate cyclase (sGC), significantly increased the development and expression of morphine tolerance, and L-NAME, a NO synthase (NOS) inhibitor, significantly decreased the development of morphine tolerance. In conclusion, these data demonstrate that the nitric oxide–cGMP signal pathway plays a pivotal role in developing tolerance to the analgesic effect of morphine.


2018 ◽  
Vol 18 ◽  
pp. 120-133 ◽  
Author(s):  
Zoltán Péterfi ◽  
Imre Farkas ◽  
Raphael G.P. Denis ◽  
Erzsébet Farkas ◽  
Motokazu Uchigashima ◽  
...  

1995 ◽  
Vol 67 ◽  
pp. 304
Author(s):  
Yasuko S. Yamashita ◽  
Kimihiro Ysamashita ◽  
Yasufumi Kataoka ◽  
Masami Niwa ◽  
Kohtaro Taniyama

2006 ◽  
Vol 23 (2) ◽  
pp. 175-177 ◽  
Author(s):  
D. Dal ◽  
M. A. Salman ◽  
A. E. Salman ◽  
A. B. Iskit ◽  
Ü. Aypar

2007 ◽  
Vol 30 (2) ◽  
pp. 67-80 ◽  
Author(s):  
Barry B. McGuire ◽  
R. William G. Watson ◽  
Fernando Pérez-Barriocanal ◽  
John M. Fitzpatrick ◽  
Neil G. Docherty

2008 ◽  
Vol 294 (3) ◽  
pp. R842-R850 ◽  
Author(s):  
Zaid Abassi ◽  
Bishara Bishara ◽  
Tony Karram ◽  
Samer Khatib ◽  
Joseph Winaver ◽  
...  

Increased intra-abdominal pressure (IAP) during laparoscopy adversely affects kidney function. The mechanism underlying this phenomenon is largely unknown. This study was designed to investigate the involvement of endothelin (ET)-1 and nitric oxide (NO) systems in IAP-induced renal dysfunction. Rats were subjected to IAP of 14 mmHg for 1 h, followed by a deflation for 60 min (recovery). Four additional groups were pretreated with 1) ABT-627, an ETA antagonist; 2) A-192621, an ETB antagonist; 3) nitroglycerine; and 4) NG-nitro-l-arginine methyl ester, a NO synthase inhibitor, before IAP. Urine flow rate (V), absolute Na+ excretion (UNaV), glomerular filtration rate (GFR), and renal plasma flow (RPF) were determined. Significant reductions in kidney function and hemodynamics were observed when IAP was applied. V decreased from 8.1 ± 1.0 to 5.8 ± 0.5 μl/min, UNaV from 1.08 ± 0.31 to 0.43 ± 0.10 μeq/min, GFR from 1.84 ± 0.12 to 1.05 ± 0.06 ml/min (−46.9 ± 2.7% from baseline), and RPF from 8.62 ± 0.87 to 3.82 ± 0.16 ml/min (−54 ± 3.5% from baseline). When the animals were pretreated with either ABT-627 or A-192621, given alone or combined, the adverse effects of IAP on GFR, RPF, V, and UNaV were significantly augmented. When the animals were pretreated with nitroglycerine, the adverse effects of pneumoperitoneum on GFR and RPF were substantially improved. In contrast, pretreatment with NG-nitro-l-arginine methyl ester remarkably aggravated pneumoperitoneum-induced renal dysfunction. In conclusion, decreased renal excretory function and hypofiltration are induced by increased IAP. These effects are related to impairment of renal hemodynamics and could be partially ameliorated by pretreatment with nitroglycerine and aggravated by NO and ET blockade.


Life Sciences ◽  
2000 ◽  
Vol 68 (4) ◽  
pp. 401-415 ◽  
Author(s):  
Marco Carmignani ◽  
Anna Rita Volpe ◽  
Paolo Boscolo ◽  
Niu Qiao ◽  
Mario Di Gioacchino ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document