bioRxiv Science⌕ Search

Biology subjects

Souto, D. E. P.

Publications and source records attributed to Souto, D. E. P..

2 recordsLinked to original sources

Morphine-induced side effects can be differentially modulated by cannabidiol in male and female rats.

Opioid use disorder (OUD) is a public health problem that includes symptoms such as withdrawal syndrome and opioid-induced hyperalgesia (OIH). Currently, drugs to treat side effects of opioids also have undesirable effects, which lead to limitations. This study investigated the effect of a treatment with cannabidiol (CBD) in morphine-induced hyperalgesia and withdrawal signs in morphine-dependent rats. Male and female rats were submitted to morphine-induced physical dependence protocol consisting of a twice daily treatment with morphine (7.89 mg/kg, 1ml/kg, s.c.) for 10 days. Nociception was measured using the hot plate test and morphine-induced thermal hyperalgesia was equally achieved following 7-10 days of morphine administration in male and female rats. Repeated treatment with CBD (30 mg/kg) was sufficient to prevent thermal hyperalgesia in male and female rats. Subsequently, rats received an acute administration of naloxone (2 mg/kg. s.c.), 90 minutes after the morphine treatment on day 11, the number of withdrawal signs was scored. Rats that received treatment exclusively with morphine presented significant withdrawal signs compared to control (Water). Morphine-dependent female rats showed a prevalent stereotyped behavior of rearing, whereas male rats had the sign of teeth chattering as the most preeminent. Treatment with CBD on day 11 partially attenuated the withdrawal signs in morphine-dependent male rats, but not female rats. Altogether, our data provide evidence of an anti-hyperalgesic effect of CBD in rats. Male and female rats treated chronically with morphine exhibited withdrawal signs in different ratios, indicating sex-differences in withdrawal behavior and CBD attenuated withdrawal signs in a sex-dependent manner.

pharmacology and toxicology↗

Sensing soluble uric acid by Naip1-Nlrp3 platform

The immune system can recognize microbes and sterile tissue damage. Among the damage-associated molecular patterns (DAMPs), uric acid is considered a major component which can trigger inflammation. It represents a breakpoint in the evolutionary history of humans as our ancestors lost the uricase gene, the enzyme responsible for its cleavage. High soluble uric acid (sUA) concentration is able to increase IL-1{beta} in murine, but not human macrophages. We observed that sUA increased the mRNA expression of Naip1 in murine macrophages, and, therefore, we hypothesized that the recognition of sUA can be made by a Naip1-Nlrp3 inflammasome platform. Additionally, we used genome-wide transcriptome analysis, functional analyses and structural modeling predictions and observed that virus-transduction of murine Naip1 into human macrophages induced IL-1{beta} after sUA stimulus, besides leading to fatty acid production and an inflammation-related response. Moreover, pharmacologic inhibition and genetic loss of Nlrp3 led to decreased IL-1{beta} production upon sUA stimulus. Surface plasmon resonance and quartz crystal microbalance showed that sUA is able to interact with Naip1. Naip could be a lost receptor for sUA in the evolutionary process and a better understanding of the immune modulatory function of sUA could lead to design rational novel anti-hyperuricemic therapies.

immunology↗