Garberg Håvard T, Solberg Rønnaug, Barlinn Jon, Martinez-Orgado Jose, Løberg Else-Marit, Saugstad Ola Didrik
Division of Pediatric and Adolescent Medicine, Department of Pediatric Research, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Neonatology. 2017;112(2):143-149. doi: 10.1159/000471786. Epub 2017 Jun 1.
Cannabidiol (CBD) is considered a promising neuroprotectant after perinatal hypoxia-ischemia (HI). We have previously studied the effects of CBD 1 mg/kg in the early phase after global HI in piglets. In contrast to prior studies, we found no evidence of neuroprotection and hypothesized that higher doses might be required to demonstrate efficacy in this animal model.
To assess the safety and potential neuroprotective effects of high-dose CBD.
Anesthetized newborn piglets underwent global HI by ventilation with 8% O2 until the point of severe metabolic acidosis (base excess -20 mmol/L) and/or hypotension (mean arterial blood pressure ≤20 mm Hg). Piglets were randomized to intravenous treatment with vehicle (n = 9) or CBD (n = 13). The starting dose, CBD 50 mg/kg, was reduced if adverse effects occurred. The piglets were euthanized 9.5 h after HI and tissue was collected for analysis.
CBD 50 mg/kg (n = 4) induced significant hypotension in 2 out of 4 piglets, and 1 out of 4 piglets suffered a fatal cardiac arrest. CBD 25 mg/kg (n = 4) induced significant hypotension in 1 out of 4 piglets, while 10 mg/kg (n = 5) was well tolerated. A significant negative correlation between the plasma concentration of CBD and hypotension during drug infusion was observed (p < 0.005). Neuroprotective effects were evaluated in piglets that did not display significant hypotension (n = 9) and CBD did not alter the degree of neuronal damage as measured by a neuropathology score, levels of the astrocytic marker S100B in CSF, magnetic resonance spectroscopy markers (Lac/NAA and Glu/NAA ratios), or plasma troponin T.
High-dose CBD can induce severe hypotension and did not offer neuroprotection in the early phase after global HI in piglets.
大麻二酚(CBD)被认为是围产期缺氧缺血(HI)后一种有前景的神经保护剂。我们之前研究了1mg/kg CBD对仔猪全脑HI后早期阶段的影响。与之前的研究不同,我们没有发现神经保护的证据,并推测可能需要更高剂量才能在该动物模型中证明其疗效。
评估高剂量CBD的安全性和潜在神经保护作用。
对新生仔猪进行麻醉,通过用8%氧气通气使其发生全脑HI,直至出现严重代谢性酸中毒(碱剩余-20mmol/L)和/或低血压(平均动脉压≤20mmHg)。仔猪被随机分为静脉注射赋形剂组(n = 9)或CBD组(n = 13)。如果出现不良反应,则降低起始剂量CBD 50mg/kg。HI后9.5小时对仔猪实施安乐死,并收集组织进行分析。
CBD 50mg/kg(n = 4)使4头仔猪中的2头出现显著低血压,4头仔猪中的1头发生致命性心脏骤停。CBD 25mg/kg(n = 4)使4头仔猪中的1头出现显著低血压,而10mg/kg(n = 5)耐受性良好。观察到药物输注期间CBD血浆浓度与低血压之间存在显著负相关(p < 0.005)。对未出现显著低血压的仔猪(n = 9)评估神经保护作用,CBD并未改变通过神经病理学评分、脑脊液中星形胶质细胞标志物S100B水平、磁共振波谱标志物(Lac/NAA和Glu/NAA比值)或血浆肌钙蛋白T所测量的神经元损伤程度。
高剂量CBD可导致严重低血压,且在仔猪全脑HI后的早期阶段未提供神经保护作用。