Author/Authors :
Asadian, Salileh Department of Toxicology - Faculty of Pharmacy - Islamic Azad University, Shahreza Branch, Shahreza, Iran , Moallem, Adel Department of Pharmacodynamics and Toxicology - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad, Iran , Moshiri, Mohammad Medical Toxicology Research Center - School of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran , Mansouri, Mustafa Department of Pharmacology & Toxicology - Faculty of Pharmacy - Pharmaceutical Sciences Branch Islamic Azad University, Tehran -Iran (IAUPS) , Ariaee-Nasab, Nazila Allergy Research Center - Mashhad University of Medical Science, Mashhad, Iran , Ghadiri, Ameneh Department of Internal Medicine and Medical Specialties - “Sapienza” University of Rome, Rome, Italy , Shahbazi, Niosha Pharmaceutical Research Center - Pharmaceutical Technology Institute - Mashhad University of Medical Sciences, Mashhad, Iran , Etemad, Leila Pharmaceutical Research Center - Pharmaceutical Technology Institute - Mashhad University of Medical Sciences, Mashhad, Iran
Abstract :
Introduction: Acetaminophen (APAP)-induced liver injury is one of the main causes of acute
liver failure in the world. Pinus eldarica is specially distributed in the north of Iran and has been
used for decades to treat wounds, pain, infection, fever, bronchitis and inflammation in many
countries. This study was undertaken to evaluate the role of pine pollen extract (PE) on APAPinduced
hepatotoxicity.
Methods: This study was conducted in two separate parts: single- and multi- dose administration
of PE. In a multiple dosing regimen, different doses of extract (10, 20, 30, 40 and 50 mg/kg) were
orally administrated for 2 weeks and then on the 15th day, the animals received a single dose of
APAP (600 mg/kg). In the second part, the highest dose of PE (50 mg/kg) was orally administrated
half an hour after receiving the APAP at dose of 600 mg/kg. The negative and positive control
groups were treated with normal saline and N-acetylcysteine (NAC), respectively. At the end
of procedure, the biochemical parameters including alanine transaminase (ALT), aspartate
transaminase (AST) and alkaline phosphatase (ALP) as well as pathological findings were
evaluated.
Results: A single and multiple oral dose of APAP increased the serum level of ALT, AST and ALP
that were significantly attenuated by PE administration in both model. Indeed, exposure to APAP
caused extensive necrosis and lymphocytic inflammation that were completely prevented by
single- and multi-dose administration of PE, specially at a high dose.
Conclusion: Finally, the present results indicate that PE could reverse the reduction of
aminotransferases and improve histological changes of APAP-induced liver toxicity. Further
research is needed to confirm this finding and reveal the exact mechanisms.
Keywords :
Toxicity , Pinus eldarica , Paracetamol , N-acetylcysteine , Hepatotoxicity , Acetaminophen