ro13-9904 has been researched along with Alcohol-Related-Disorders* in 2 studies
1 review(s) available for ro13-9904 and Alcohol-Related-Disorders
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Meningitis caused by Capnocytophaga canimorsus: when to expect the unexpected.
In this article we review the available data concerning meningitis caused by Capnocytophaga canimorsus. The clinical presentation of this rare condition is described with the emphasis on associated conditions and management issues. Two additional cases, illustrating the difficulties in recognizing this rare disease, are presented. Reviewing a total of 28 reported cases, a preceding bite-incident by a cat or dog, or close contact with these animals, was described in the majority of cases (89%). Patients had a median age of 58 years; splenectomy and alcohol abuse were noted in, respectively, 18% and 25% of patients. Only in one case immune suppressive drug use was reported. The diagnosis C. canimorsus meningitis should be considered in healthy and immunocompromised adults, especially after splenectomy, who present with symptoms attributable to meningitis and a history of recent exposure to dogs or cats. The possibility of this condition has implications for both the diagnostic work-up and the treatment of the patient. Topics: Alcohol-Related Disorders; Animals; Bites and Stings; Capnocytophaga; Cats; Ceftriaxone; Dexamethasone; Diagnosis, Differential; Dogs; Drug Therapy, Combination; Gram-Negative Bacterial Infections; Humans; Male; Meningitis, Bacterial; Middle Aged; Opportunistic Infections; Risk Factors; Splenectomy | 2007 |
1 other study(ies) available for ro13-9904 and Alcohol-Related-Disorders
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Effects of ceftriaxone on hydrocodone seeking behavior and glial glutamate transporters in P rats.
Hydrocodone (HYD) is one of the most widely prescribed opioid analgesic drugs. Several neurotransmitters are involved in opioids relapse. Among these neurotransmitters, glutamate is suggested to be involved in opioid dependence and relapse. Glutamate is regulated by several glutamate transporters, including glutamate transporter 1 (GLT-1) and cystine/glutamate transporter (xCT). In this study, we investigated the effects of ceftriaxone (CEF) (200 mg/kg, i.p.), known to upregulate GLT-1 and xCT, on reinstatement to HYD (5 mg/kg, i.p.) using the conditioned place preference (CPP) paradigm in alcohol-preferring (P) rats. Animals were divided into three groups: 1) saline-saline group (SAL-SAL); 2) HYD-SAL group; and 3) HYD-CEF group. The CPP was conducted as follows: habituation phase, conditioning phase with HYD (i.p.) injections every other day for four sessions, extinction phase with CEF (i.p.) injections every other day for four sessions, and reinstatement phase with one priming dose of HYD. Time spent in the HYD-paired chamber after conditioning training was increased as compared to pre-conditioning. There was an increase in time spent in the HYD-paired chamber with one priming dose of HYD in the reinstatement test. HYD exposure downregulated xCT expression in the nucleus accumbens and hippocampus, but no effects were observed in the dorsomedial prefrontal cortex and amygdala. Importantly, CEF treatment attenuated the reinstatement effect of HYD and normalized xCT expression in the affected brain regions. These findings demonstrate that the attenuating effect of HYD reinstatement with CEF might be mediated through xCT. Topics: Alcohol-Related Disorders; Amino Acid Transport Systems, Acidic; Animals; Ceftriaxone; Central Nervous System Agents; Conditioning, Psychological; Drug-Seeking Behavior; Excitatory Amino Acid Transporter 1; Excitatory Amino Acid Transporter 2; Genetic Predisposition to Disease; Hippocampus; Hydrocodone; Male; Neuroglia; Nucleus Accumbens; Opioid-Related Disorders; Rats; Species Specificity | 2018 |