牡蛎的比较解剖学及系统分类和演化的研究

本文对我国己发表的牡蛎作了详细的比较解剖学研究。在强蛎亚科（Pycnodonteinae）发现了第三个心耳－－右上心耳和与其相连的第三条回心静脉－－后静脉，这在双壳类中实属首次报道。第一次提出了牡蛎循环系统的两种类型，附心脏型和无附心脏型。两者之间的主要区别是：前者无肌套血管，其外套血液主要来自环外套动脉和附心脏，而后者由于无附心脏和环外套动脉，其外套血液主要来自肌套血管；前者是通过出鳃静脉和外套静脉分别将鳃前部和后部的血液送回心耳，而后者的外套静脉与外入鳃血管不通，鳃中的血液只能通过出鳃静脉回到心耳。根据外套腔的形态特点，本文将中国的牡蛎分为三种类型六个组。第一种类型，左右侧都具侧水腔，包括一个组；第二种类型，仅右侧具有侧水腔，包括四个组；第三种类型；不具侧水腔，包括一个组。在比较解剖学研究的基础上，文章还讨论了消化系统，神经系统，循环系统等一些主要系统的演化过程，并推测了现生牡蛎各属间的演化关系。提出了一些新的分类依据，发现了一个具有重要演化意义的单行属种，爪蛎属（Talonostrea），猫爪牡蛎（T. talonata）。澄清了目前世界上在舌骨蛎属（Hyotissa）、拟舌骨蛎属（Parahyotissa）、小蛎属（Saccostrea）和巨蛎属（Crassostrea）分类中的混乱。解决了我国牡蛎分类中存在己久的疑难问题，将己发表的20种牡蛎重新鉴定为15种，即舌骨牡蛎（Hyotissa hyotis），复瓦牡蛎（Parahyotissa imbricata）。中华牡蛎（P. sinensis），鸡冠牡蛎（Lopha cristagalli）。薄片牡蛎（Dendostren folium），缘齿牡蛎（D. cre-nulifera），褶牡蛎（Alectryonella plicatula），猫爪牡蛎（T. talonata），长牡蛎（Crassostrea gigas），近江牡（C. rivularis），拟近江牡蛎（Crassostrea sp.），僧帽牡蛎（Saccostrea cucullata），棘刺牡蛎（S. echinata），鹅掌牡蛎（Planostrea pestigris）和密鳞牡蛎（Ostrea denselamellosa）。它们分别隶属于二个科，曲蛎科（Grypheidae）和牡蛎科（Ostreidae）；四个亚科，强蛎亚科（Pycnodonteinae）。冠蛎亚科（Pycnodonteinae），巨蛎亚科（Lopheinae）和牡蛎亚科（Crassostreinae）。

细胞外信号调节蛋白激酶-cAMP反应元件结合蛋白信号通路在应激所致抑郁行为障碍中的作用

Stress is the most important factor in the vulnerability to depression and other behavioral disorders, but the mechanisms that stress signals are transferred into depression are far from understanding. To date, the neurotransmitters, neurotrophins and signal pathway have been concerned in the topic focusing on the pathophysiology of depression, but there are still many puzzles. Increasing evidence has indicated that the alteration in neuronal plasticity is the “trace” of stress-induced damages. The extracellular signal-regulated protein kinase(ERK)-cyclic-AMP-responsive element（CRE）-binding protein(CREB)signal pathway is a powerful intracellular signal transduction pathway participating in neuronal plasticity which is involved in higher brain cognitive functions such as learning and memory. However, so far, little is known about the role of the ERK-CREB signal pathway in response to stress and emotional modulations. Thus the aim of the study was to systematically investigate the role of the ERK-CEB signal pathway in depressive-like behaviors induced by stress. Depression animal models, antidepressant agent treatment and disruption of signal pathway in specific brain regions were applied. In the present study, three experiment sessions were designed to make sure whether the ERK-CREB signal pathway was indeed one of pathophysiological mechanisms of depressive-like behaviors induced by stress. In experiment one, two different stress animal models were applied, chronic forced swim stress and chronic empty water bottle stress. After stress, all animals were tested behaviorally using open-field, elevated-plus maze and saccharine preference test, and brain samples were processed for determination of ERK, P-ERK, CREB and P-CREB using western blot. The relationships between the proteins of ERK, P-ERK, CREB and P-CREB in the brain and the behavioral variables were also analyzed. In experiment two, rats were treated with antidepressant agent fluoxetine once a day for 21 consecutive days, then the brain levels of ERK, P-ERK, CREB and P-CREB was determined, the depressive-like behaviors were also examined. In experiment three, mitogen activated extracellular-signal-regulated kinase kinase (MEK) inhibitor U0126 was administrated to inhabit the activation of ERK in the hippocampus and prefrontal cortex respectively, then behavioral measurements and protein detection were conducted. The main results of the study were as the following: (1) Chronic forced swim stress induced animals to suffer depression and disrupted the ERK-CREB signal pathway in hippocampus and prefrontal cortex. There were significant correlations between P-ERK2, P-CREB and multiple variables of depressive-like behaviors. (2) Chronic empty water bottle stress did not induce depressive-like behaviors. Such stress decreased the brain level of P-ERK2 in hippocampus and prefrontal cortex, but the level of P-CREB in the hippocampus was increased. (3) The antidepressant agent fluoxetine relieved depressive-like behaviors and increased the activities of the ERK-CREB signal pathway in stressed animals. (4) Animals treated with U0126 injection into hippocampus showed decreased activities of the ERK-CREB signal pathway in the hippocampus, and suffered depression comorbid with anxiety. (5) Animals treated with U0126 injection into prefrontal cortex showed decreased activities of the ERK-CREB signal pathway in the prefrontal cortex, and exhibited depressive-like behaviors. In conclusion, The ERK-CREB signal pathway in the hippocampus and prefrontal cortex was involved in stress responses and significantly correlated with depressive-like behaviors; The ERK-CREB signal pathway in the hippocampus and prefrontal cortex participated in the mechanism that fluoxetine reversed stress-induced behavioral disorders, and might be the target pathway of the therapeutic action of antidepressants; The disruption of the ERK-CREB signal pathway in the hippocampus or prefrontal cortex led to depressive-like behaviors in animals, suggesting that disruption of ERK-CREB pathway in the hippocampus or prefrontal cortex was involved in the pathophysiology of depression, and might be at least one of the mechanisms of depression induced by stress.