“在哪里”和“有多少”? 中国雪豹调查与空缺

雪豹(Panthera uncia)分布广泛且调查难度较大, 全世界的雪豹研究面临的首要问题是雪豹基础数据的缺乏。本文通过检索1980至2018年已发表的含有中国境内雪豹分布和密度信息的中英文文章共35篇, 从中提取出雪豹的分布与密度信息, 其中含有密度估计的文献18篇。同时, 来自雪豹调查的15位一线成员通过填写表格和问卷的形式提供了28个地块上未发表的雪豹密度调查信息。基于此, 我们逐一分析了各省份已有的雪豹调查现状和存在的调查空缺, 发现雪豹分布调查的两大空白区域主要存在于与吉尔吉斯斯坦接壤的西天山地区和西藏南部的冈底斯-念青唐古拉山山脉和喜马拉雅山脉。相对我国雪豹栖息地总面积, 有过密度估算的面积仅占1.7%, 仍然处于刚刚起步的阶段, 并且已有的密度调查几乎都是在质量较好的雪豹栖息地内进行的。今后除了需要继续努力收集汇总已有的调查结果, 仍然需要在雪豹分布区(特别是空缺区域)内增加调查。     

Cd2+胁迫对银芽柳PSⅡ叶绿素荧光光响应曲线的影响

以盆栽银芽柳为材料,利用MINI-IMAGING-PAM荧光成像测定系统,研究了Cd²⁺胁迫下叶片叶绿素荧光参数的变化及其光响应曲线。结果表明,初始荧光Fo与最大荧光Fm随着Cd²⁺浓度的增大而呈现先升后降的趋势,Fo与Fm在200 mg/LCd²⁺处理4周时达到最高值,400 mg/LCd²⁺处理则显著下降;PSⅡ最大光化学效率(Fv/Fm)与PSⅡ潜在光化学效率(Fv/Fo)显著受 Cd²⁺胁迫抑制,但随Cd²⁺浓度的增加呈先降后升的变化趋势。Cd²⁺胁迫下各叶绿素荧光参数的光响应结果表明,PSⅡ实际光量子效率Y(Ⅱ)、荧光淬灭系数(qP)随光化光强度的增加呈下降趋势,而同光强下高浓度Cd²⁺ 使Y(Ⅱ)与(qP) 显著降低;PSⅡ调节性能量耗散的量子产额Y(NPQ)、非光化学淬灭系数(qN)与表观电子传递速率(ETR)则随着光强增加呈上升趋势,同光强下高浓度Cd²⁺处理显著提高Y(NPQ)、qN 与ETR。Cd²⁺胁迫下,PSⅡ非调节性能量耗散的量子产额Y(NO)稳定在较低水平,同光强下Y(NO)随Cd²⁺浓度增加略有提高。说明,银芽柳通过调节PSⅡ反应中心开放程度与活性,对Cd²⁺胁迫表现出较强的耐性,高浓度Cd²⁺胁迫导致PSⅡ反应中心关闭或不可逆失活,表现出光抑制。     

The Neuroprotective Roles of Sonic Hedgehog Signaling Pathway in Ischemic Stroke

Ischemic stroke is characterized by high morbidity, mortality and disability rate worldwide. Because of its complexity in pathogenesis and lack of effective therapeutic strategies and drugs, great breakthrough has not yet been made in the treatment of cerebral ischemic stroke. Therefore, to explore a more effective and safer therapeutic strategy for cerebral ischemic stroke has been the focus of numerous researchers. Neuroprotective effects of sonic hedgehog (Shh) signaling pathway in ischemic stroke have been reported in recent studies, but have not been fully elucidated. In our review, we elaborate the roles of Shh signaling in ischemic stroke from different aspects, including oxidative stress, excitotoxicity, neuroinflammation, apoptosis, angiogenesis, neuroplasticity, neurogenesis, astrogliosis and oligodendrogenesis. Meanwhile, Shh signaling based therapeutic approaches for cerebral ischemic stroke are also included in our review. We hope it will benefit the readers to better understand the roles of Shh signaling pathway in cerebral ischemic stroke and provide more comprehensive insights for basic research and novel strategies for the clinical treatment of cerebral ischemic stroke.     

Evidence for histamine as a neurotransmitter in the cardiac sympathetic nervous system

The colocalization of histamine (HA) and norepinephrine (NE) immunoreactivities was identified within the superior cervical ganglia neurons of the guinea pig. HA and NE immunoreactivity levels were significantly attenuated after chemical sympathectomy with 6-hydroxydopamine (6-OHDA). Coexistence of NE and HA was also visualized in the cardiac sympathetic axon and varicosities labeled with anterograde tracer biotinylated dextran amine. Depolarization of cardiac sympathetic nerve endings (synaptosomes) with 50 mM potassium stimulated endogenous HA release, which was significantly attenuated by 6-OHDA or a vesicular monoamine transporter 2 (VMAT2) inhibitor reserpine pretreatments. Compound 48/80, a mast cell releaser, did not affect cardiac synaptosome HA exocytosis. Furthermore, K+ -evoked HA release was abolished by the N-type Ca2+ -channel blocker omega-conotoxin but was not affected by the L-type Ca2+ -channel blocker lacidipine. Cardiac synaptosome HA exocytosis was augmented by the enhanced synthesis of HA or the inhibition of HA metabolism. HA H3-receptor activation by (R)-alpha-methylhistamine inhibited high K+ -evoked histamine release. The HA H3 receptor antagonist thioperamide enhanced K+ -evoked HA release and blocked the (R)-alpha-methylhistamine effect. The K+ -evoked endogenous NE release was attenuated by preloading the cardiac synaptosomes with L-histidine or quinacrine. These inhibitory effects were reversed by thioperamide or antagonized by alpha-fluoromethylhistidine. Our findings indicate that high K+ -evoked corelease of NE and HA may be inhibited by endogenous HA via activation of presynaptic HA H3-receptors. The H3-receptor may function as an autoreceptor, rather than a heteroreceptor, in the regulation of sympathetic neurotransmission and HA may be a novel sympathetic neurotransmitter.     

A substantia innominata-midbrain circuit controls a general aggressive response

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