Mierzejewski Pawel, Zakrzewska Alicja, Kuczyńska Julita, Wyszogrodzka Edyta, Dominiak Monika
Department of Pharmacology, Institute of Psychiatry and Neurology, Warsaw, Poland.
PeerJ. 2020 Sep 11;8:e9886. doi: 10.7717/peerj.9886. eCollection 2020.
Alcohol drinking may be associated with an increased risk of various metabolic diseases. Rat lines selectively bred for alcohol preference and alcohol avoidance constitute an interesting model to study inherited factors related to alcohol drinking and metabolic disorders. The aim of the present study was to compare the levels of selected laboratory biomarkers of metabolic disorders in blood samples from naïve offspring of Warsaw alcohol high-preferring (WHP), Warsaw alcohol low-preferring (WLP), and wild Wistar rats. Blood samples were collected from 3-month old (300-350 g) alcohol-naïve, male offspring of WHP ( = 8) and WLP rats ( = 8), as well as alcohol-naïve, male, wild Wistar rats. Markers of metabolic, hepatic, and pancreatic disorders were analysed (levels of homocysteine, glucose, total cholesterol, triglycerides and -glutamyl transferase (GGT), aspartate (AST), alanine aminotransferase (ALT), and amylase serum activities). Alcohol-naïve offspring of WHP, WLP, and wild Wistar rats differed significantly in the levels of triglycerides, total cholesterol, homocysteine, as well as in the activity of GGT, ALT, AST, and amylase enzymes. Most markers in the alcohol-naïve offspring of WHP rats were altered even thought they were never exposed to alcohol pre- or postnatally. This may suggest that parental alcohol abuse can have a detrimental influence on offspring vulnerability to metabolic disorders.
饮酒可能与多种代谢性疾病风险增加有关。选择性培育出偏好酒精和回避酒精的大鼠品系,构成了一个有趣的模型,用于研究与饮酒及代谢紊乱相关的遗传因素。本研究的目的是比较来自华沙高酒精偏好(WHP)、华沙低酒精偏好(WLP)和野生Wistar大鼠的未接触过酒精的子代血液样本中选定的代谢紊乱实验室生物标志物水平。从3个月大(300 - 350克)未接触过酒精的WHP(n = 8)和WLP大鼠(n = 8)的雄性子代以及未接触过酒精的雄性野生Wistar大鼠中采集血液样本。分析代谢、肝脏和胰腺紊乱的标志物(同型半胱氨酸、葡萄糖、总胆固醇、甘油三酯以及γ-谷氨酰转移酶(GGT)、天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)和淀粉酶的血清活性水平)。WHP、WLP和野生Wistar大鼠未接触过酒精的子代在甘油三酯、总胆固醇、同型半胱氨酸水平以及GGT、ALT、AST和淀粉酶的活性方面存在显著差异。WHP大鼠未接触过酒精的子代中的大多数标志物都发生了改变,即使它们在出生前和出生后都从未接触过酒精。这可能表明亲代酒精滥用会对后代患代谢紊乱的易感性产生不利影响。