|1.||Baeyens, José M: 2 articles (01/2014 - 03/2013)|
|2.||Cendán, Cruz M: 2 articles (01/2014 - 03/2013)|
|3.||Baeyens, José Manuel: 2 articles (11/2012 - 06/2009)|
|4.||Entrena, José Manuel: 2 articles (11/2012 - 06/2009)|
|5.||Zamanillo, Daniel: 2 articles (11/2012 - 06/2009)|
|6.||Nieto, Francisco Rafael: 2 articles (11/2012 - 06/2009)|
|7.||Cobos, Enrique José: 2 articles (11/2012 - 06/2009)|
|8.||Cendán, Cruz Miguel: 2 articles (11/2012 - 06/2009)|
|9.||Steardo, Luca: 1 article (01/2015)|
|10.||Hayashi, T: 1 article (01/2015)|
|1.||Body Weight (Weight, Body)
01/01/2015 - "Administration of the selective Sig-1R antagonist BD-1063 dramatically reduced the acquisition of alcohol drinking behavior as well as the preference for alcohol in genetically selected TSRI Sardinian alcohol preferring (Scr:sP) rats; the treatment had instead no effect on total fluid intake, food intake or body weight gain, proving selectivity of action. "
10/01/2014 - "administration of BD-1063 or S1RA had no effect on thermal hyperalgesia in σ1-KO mice, supporting on-target mechanisms for the effects of both drugs. "
10/01/2014 - "The subcutaneous (s.c.) administration of the selective σ1 antagonists BD-1063 and S1RA to wild-type mice dose-dependently and fully reversed inflammatory mechanical (paw pressure) and thermal (radiant heat) hyperalgesia. "
03/01/2013 - "Subcutaneous administration of the σ1 receptor antagonists BD-1063 (16-64 mg/kg), S1RA (32-128 mg/kg), and NE-100 (8-64 mg/kg) dose-dependently reduced the number of behavioral responses (by 53, 62, and 58%, respectively) and reversed the referred hyperalgesia to mechanical control threshold (0.53 ± 0.05 g) in WT mice. "
11/01/2012 - "The administration of BD-1063 or S1RA 30 minutes before each paclitaxel dose prevented the development of cold and mechanical allodynia in WT mice. "
06/01/2009 - "The high-affinity and selective sigma(1) antagonists BD-1063, BD-1047 and NE-100, administered subcutaneously (s.c.), dose-dependently inhibited mechanical allodynia induced by capsaicin (1 microg,i.pl.), yielding ED(50) (mg/kg) values of 15.80+/-0.93, 29.31+/-1.65 and 40.74+/-7.20, respectively. "
03/01/2013 - "The authors evaluated the role of σ1 receptors in intracolonic capsaicin-induced visceral pain (pain-related behaviors and referred mechanical hyperalgesia to the abdominal wall) using wild-type (WT) (n = 12 per group) and σ1 receptor knockout (σ1-KO) (n = 10 per group) mice, selective σ1 receptor antagonists (BD-1063, S1RA, and NE-100), and control drugs (morphine and ketoprofen). "
|4.||Neuralgia (Stump Neuralgia)
|4.||N,N- dipropyl- 2- (4- methoxy- 3- (2- phenylethoxy)phenyl)ethylamine monohydrochloride
|5.||Morphine (MS Contin)