Jun 2026· Tikrit journal of pharmaceutical sciences· Vol 20, pp. 33-42· 0 citations
TL;DR
It is demonstrated that both histopathological and biochemical manifestations that were induced following ketamine administration have been attenuated by using palmitoleic acid as prophylaxis, indicating that palmitoleic acid could show marked protective effects against ketamine-induced liver damage in rats.
Abstract
Background: Palmitoleic acid has cytoprotective effects against different insults. This study examined the protective benefits of palmitoleic acid against ketamine-induced hepatic damage in rats by biochemical and histological evaluations.
Methods: In the current study, thirty-six albino male gender rats aged 12-14 weeks were used and divided into four equal groups, each with nine rats: Control, Ketamine, Palmitoleic acid only, and Palmitoleic acid + ketamine. Palmitoleic acid was given orally by gavage at a dosage of 300mg/kg/day for seven days consecutively. On days 8 & 9, ketamine was injected intraperitoneally at a dosage of 160mg/kg/day. Haematoxylin and eosin staining was employed to examine liver tissues microscopically. Additionally, serum liver enzymes were evaluated, such as gamma-glutamyl transferase (GGT) level, alanine aminotransferase (ALT) level, and aspartate aminotransferase (AST) level.
Results: In comparison to the control, the injection of ketamine caused significant elevations in serum ALT (65.41±8.74U/L), AST (153.97±20.65U/L), and GGT (3.36±0.53U/L) (p < 0.001). This suggests that the liver damage was substantial. Histopathological analysis of the ketamine-treated cohort demonstrated oncotic and coagulative necrosis, widespread hydropic degeneration, pronounced inflammatory cell infiltration, and vascular congestion. Palmitoleic acid pretreatment greatly mitigated these alterations, lowering ALT, AST, and GGT levels to near-control values and substantially enhancing hepatic histoarchitecture, with very slight residual inflammatory infiltration and minimal degenerative effects.
Conclusions: The findings of this study demonstrated that both histopathological and biochemical manifestations that were induced following ketamine administration have been attenuated by using palmitoleic acid as prophylaxis. This indicates that palmitoleic acid could show marked protective effects against ketamine-induced liver damage in rats.
Objective. Omega-7 fatty acids have offered promising hepatoprotective properties in various experimental models. This study aimed to investigate the prophylactic potential of omega-7 supplementation against doxorubicin (Dox)-induced hepatic injury in albino rats. Methods. A total of 42 rats were divided into 6 groups (7 animals each), namely control, Dox (15mg/kg, single IP dose at day 7), glycerin group, omega-7 (100mg/kg/day), omega-7 (100mg/kg/day, oral gavage) plus Dox, and omega-3 (100mg/kg/day) plus Dox. The groups were treated for 14 days with either normal saline alone, glycerin alone, omega-7 or omega-3 with intervention by Dox single dose at day-7 for omega groups only. Hepatic injury was assessed via biochemical parameters, including liver parameters, oxidative stress markers, inflammatory cytokines, and histopathological examination of liver tissues. Results. Omega-7 pretreatment resulted in a significant reduction of mean serum hepatic enzymes (ALT: vs. Dox alone, p<0.0001; ALP: vs. Dox alone, p<0.0001; AST: vs. Dox alone, p<0.001). Omega-7 modulated oxidative stress status, indicated by reduced mean MDA (P<0.001) compared to Dox alone and increased TAS (vs. Dox alone, p<0.0001). The elevated proinflammatory markers (TNFα and IL-1β) induced by Dox were significantly (p<0.0001) mitigated by omega-7. Histological analysis revealed severe hepatocellular degeneration, necrosis, and inflammatory infiltration. Histopathological examination showed preservation of hepatic architecture with minimal inflammatory changes in the omega-7 pre-treated group. Conclusion. Omega-7 offered prophylactic anti-inflammatory benefit against Dox-induced hepatic injury, confirmed by histological and biochemical findings.
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