Ozone Exposure Controls Oxidative Stress and the Inflammatory Process of Hepatocytes in Murine Models.

(1) Background: Ozone exposure is a promising tool for treating liver damage since it is known to control the release of free radicals and increase the expression of antioxidant enzymes. The objective is to investigate the main intracellular pathways activated after exposure to ozone, considering the dosage of antioxidant enzymes and markers of oxidative stress. (2) Methods: This systematic review was performed based on the PRISMA guidelines and using a structured search in MEDLINE (PubMed), Scopus, and Web of Science. Bias analysis and methodological quality assessments were examined using the SYRCLE Risk of Bias tool. (3) Results: Nineteen studies were selected. The results showed that the exposure to ozone has a protective effect on liver tissue, promoting a decrease in inflammatory markers and a reduction in oxidative stress in liver tissue. In addition, ozone exposure also promoted an increase in antioxidant enzymes. The morphological consequences of controlling these intracellular pathways were reducing the tissue inflammatory process and reducing areas of degeneration and necrosis. (4) Conclusions: Ozone exposure has a beneficial effect on models of liver injury through the decrease in oxidative stress in tissue and inflammatory markers. In addition, it regulates the Nrf2/ARE antioxidant pathway and blocks the NF-κB inflammatory pathway.

Schizocalyx cuspidatus (A. St.-Hil.) Kainul. & B. Bremer extract improves antioxidant defenses and accelerates the regression of hepatic fibrosis after exposure to carbon tetrachloride in rats.

The aim of this study was to investigate the effect of leaves extract of Schizocalyx cuspidatus (A. St.-Hil.) Kainul. & B. Bremer on hepatic morphofunctional dysfunction induced by carbon tetrachloride (CCl4). Liver lesions were induced via intraperitoneal administration of CCl4 every 48 h for 12 days. Forty-nine rats were randomised into seven groups: G1: CCl4; G2: CCl4 (animals euthanised 24 h after last CCl4 application); G3: CCl4 + DMSO; G4: SCE 400 mg/kg; G5: DMSO (700 µl); G6: CCl4 + SCE 200 mg/kg and G7: CCl4 + SCE 400 mg/kg. SCE administration resulted in reduction in hydroperoxide levels, lipidic droplets and necrosis compared to G1, G2 and G3. There was an increase in the amount of collagen fibres in G1, G2 and G3 compared to the groups. These results show that the extract of SCE leaves has great potential for the recovery of liver damage after the application of CCl4.

Bark Extract of Bathysa cuspidata in the Treatment of Liver Injury Induced by Carbon Tetrachloride in Rats

The aim of this study was to investigate the effect of bark extract Bathysa cuspidata (BCE) in the reconstitution of hepatic parenchyma and stroma after dysfunction induced by the CCl4. Liver lesions were induced by intraperitoneal administration of CCl4 (1 mL/kg) every 48 h for 12 days. The animals were treated with B. cuspidata extract (BCE) administered by gavage for another 12 days. Forty-nine rats were randomized into seven treatment groups with seven animals receiving CCl4, BCE (200, or 400 mg/kg) and the vehicle DMSO alone, or in different combinations. The extract alone showed no evidence of hepatic toxicity. In general, rats acutely exposed to CCl4 without the treatment with BCE presented high ALT and AST serum levels and high tissue content of lipid hydroperoxides, malondialdehyde, and lipid droplets. BCE administration, especially at 400 mg/kg attenuated significantly all these parameters. Furthermore, the antioxidant activities of the enzymes superoxide dismutase and catalase were significantly increased in the groups receiving this extract. These results showed that the extract of B. cuspidata stem bark stimulated the antioxidant defense system and reduced the morphological and functional liver damage in Wistar rats previously exposed to CCl4.

Influência do laser arseneto de gálio e arseneto de gálio-alumínio e pomada cicatrizante sobre leucócitos sanguíneos de ratos Wistar após lesão cutânea / Influence of the gallium arsenide laser and gallium aluminum arsenide laser and healing ointment on blood leukocytes in Wistar rats after cutaneous lesion

O presente estudo avaliou os efeitos do laser arseneto de gálio-alumínio (GaAsAl), do laser arseneto de gálio (GaAs) e pomada cicatrizante DersaniÒ sobre leucócitos sanguíneos após realização de feridas cutâneas em ratos Wistar. Os parâmetros analisados foram os valores hematológicos dos animais. Foram utilizados 30 ratos Wistar, adultos jovens, machos, provenientes da Universidade Federal de Viçosa. Cinco feridas de 12 mm foram feitas na região dorsal do ratos. Os animais foram separados em 5 grupos, com 6 animais cada. Grupo 1: animais tratados com o laser GaAs (4J/cm2), grupo 2: laser GaAsAl (30J/cm2), grupo 3: laser GaAsAl (60J/cm2), grupo 4: foi usada pomada DersaniÒ grupo 5: solução salina (controle). As aplicações foram feitas diariamente durante 20 dias. Foi coletado sangue no primeiro e último dia do experimento e foi armazenado com anticoagulante. A contagem global de leucócitos foi feita utilizando câmera de Neubauer. A contagem diferencial foi feita através de esfregaço após coloração com Giemsa. A contagem global de leucócitos nos diferentes tratamentos não apresentou diferença significativa, exceto nos animais tratados com DersaniÒ em que houve aumento significativo no número de monócitos. Os tratamentos com salina e Laser GaAsAl 30J/cm2 também apresentaram aumento no número de neutrófilos.

This study evaluated the effect of the gallium aluminum arsenide laser (GaAsAl), gallium arsenide laser (GaAs) and healing ointment Dersani® on blood leukocytes after performing cutaneous incision in Wistar rats. The analyzed parameters were the hematological values of the animals. 30 Wistar rats, young, adults, males, from Federal University of Viçosa, MG were used. Five incisions (12 mm long) were made in the dorsal region of the rats. The animals were divided into five groups, with six animals each. Group 1: animals treated with the GaAs laser (4J/cm2); Group 2: GaAsAl laser (30 J/cm2); Group 3: GaAsAl laser (60 J/cm2); Group 4: the DersaniÒ ointment was used; Group 5: saline solution (control). Therapy was applied daily for a period of 20 days. Blood samplings were carried out on the first and last day of the experiment and stored with anticoagulant. Total leukocytes count was performed using a Neubauer camera. Differential counts of Giemsa-stained smears were made. Total leukocytes count did not show significant difference in any treatment, except in the animals treated with Dersani® that a significant increase in monocytes number was found. The treatment with saline and the GaAsAl (30 J/cm2) laser showed also an increase in the number of neutrophils.