果蠅(Drosophila melanogaster)的習得性無助表現之研究
習得性無助是個體經多次追求獎賞或逃離困境失敗後產生的一種消極行為表現。習得性無助的行為研究雖多,但對其神經機制的研究卻甚少。 本研究發現273,cha-Gal80>CsC-mCh是適合光遺傳學訓練的果蠅殖系。在白光點獎賞記憶訓練中,使273,cha-Gal80>CsC-mCh果蠅學會白光點視覺訊號代表著獎賞,並發現其白光獎賞記憶能持續7分鐘以上但未達10分鐘。藉已建立白光視覺訊號與獎賞連結的273,cha-Gal80>CsC-mCh,發現重複追求獎賞失敗的實驗組,相較於持續接受獎賞與完成獎賞記憶訓練而無任何操作的對照組,明顯表現習得性無助,本研究亦發現習得性無助個體也表現了活動力、覓食表現及攝食動機的下降。 本研究成功建立高成效的果蠅成蟲光遺傳學習得性無助訓練,並針對果蠅成蟲的習得性無助行為表現進行完整的研究,未來期望本於此訓練方式進行特定腦區、神經群和神經傳遞物之探究,建構果蠅習得性無助的神經網路機制。
大「逆」不道—局部逆境下植物體內傳訊與物質分配機制
When a leaf of a plant encounters stress, how does the plant convey the stress signal to other tissues and manage nutrient distribution? This field of study has been largely unexplored. However, the unique interconnected frond structure of Lemna trisulca, along with the use of a divided Petri dish, is very suitable for handling localized stress and investigating the mechanisms of intracellular signaling and nutrient distribution. Research has shown that when the mother leaf experiences localized stress, it releases healthy daughter leaves to minimize collateral damage to the daughter leaves. Conversely, when the daughter leaves face localized stress, the mother leaf chooses to retain them and continues supplying them with nutrients to support their survival. In-depth studies revealed that stressed daughter leaves accumulate Reactive Oxygen Species (ROS), triggering nutrient distribution by sending a distress signal to the mother leaf. This prompts the mother leaf to use Ca2+ as a signaling molecule to deliver nutrients to the daughter leaves. Selective detachment is regulated and triggered by the interaction between Ca2+ and ROS within the mother leaf. When the mother leaf undergoes stress, Ca2+ acts upstream to induce ROS accumulation at the nodes, sending a unidirectional detachment signal to the daughter leaves. This causes ROS accumulation at the daughter leaf nodes, inducing detachment and thereby reducing the collateral damage the daughter leaf could experience due to the mother leaves.
Let There Be (Optimal) Light
On average, the agricultural sector uses 70% of water withdrawals worldwide to produce crops1 and contributes to the eutrophication of lakes by using nutrients that are leached from the soils into lakes and reservoirs2. Vertical farming has great potential to remedy some of these issues. By growing plants vertically in controlled environments with artificial light and reusing the water, vertical farms use op to 99% less water3 and can produce up to 10 times the yield per square meter4 compared to traditional greenhouses. This improved efficiency comes at a cost; on average, vertical farms use more than 600% more energy per kilogramme of crop compared to traditional greenhouses5. 55% of this energy use is due to the use of artificial lighting6. Even though a lot of research is conducted on yield optimisation of crops in vertical farming, few research articles focus on the growth efficiency of crops to reduce the energy use in vertical farms. Only a few previous studies have tested photoperiods under 10 h·d-1. This study focuses on reducing the energy costs of light use in vertical farms by finding the photoperiod with highest energy use efficiency for the leafy vegetable arugula (eruca sativa). Energy use efficiency is defined as fresh mass per unit of electricity input (measured in kWh). In this study, arugula plants were exposed to LED growth light, with photoperiods ranging from 0 h·d-1 to 24 h·d-1 (0 h·d-1, 4 h·d-1, 7 h·d-1, 9 h·d-1, 12 h·d-1, 14 h·d-1, 16 h·d-1 and 24 h·d-1) and a PPFD of 800 μmol·m-2·s-1. The photoperiod 7 h·d-1 had the highest energy use efficiency of all photoperiods and, if used in vertical farms, this could account for approximately a 10 percent decrease in energy per kilogramme used in vertical farms (a 4 kWh decrease), with the planting density of 1400 plants per m2. This could amount to a yearly energy saving of 4,000,000 kWh per vertical farm (based on the yearly harvest of the vertical farm Nordic Harvest). This could help make vertical farming a more sustainable plant production for the future and in turn, help farming protect our water resources instead of consuming and polluting.
金屬多酚配位奈米載體合成與多功能腫瘤治療法開發
本研究結合奈米合成技術與生物醫學, 利用表沒食子兒茶素沒食子酸酯 (Epigallocatechin gallate, EGCG) 作為載體 調控摻雜Cu2+/Cu3+與 Fe2+/Fe3+之含量 並以π-π交互作用力附載缺氧性抗癌藥物替拉扎明 (Tirapazamine, TPZ) 成功製備出多功能金屬多酚配位奈米顆粒簡稱為EFeCuTPZ。 材料經紫外-可見光譜 (UV-vis),、動態光散射 (DLS) 及掃描式電子顯微鏡 (SEM) 確認其粒徑大小、形貌學與穩定性。利用808 nm和671 nm雷射分析其光熱轉換效率 評估光熱療法效果,。在腫瘤微酸性環境下, EFeCuTPZ可利用高濃度之H2O2行芬頓反應 (Fenton Reaction) 產生高活性之氫氧自由基 (•OH), 展現化學動力療法 (Chemo dynamic-therapy, CDT),。同時, 藉由材料中的Cu²⁺與腫瘤環境中的穀胱甘肽 (Glutathione, GSH)反應減少高活性物質 (Reactive oxygen species, ROS) 的消耗 增強CDT之療效。酸性條件下 TPZ顯著釋放 有助於腫瘤治療。 另外, 細胞實驗顯示EFeCuTPZ具有高生物相容性與治療效果, 成功開發出具CDT,、CT及PTT功能之奈米複合材料 為醫學新興藥物材料提供可能性。
大「逆」不道—局部逆境下植物體內傳訊與物質分配機制
When a leaf of a plant encounters stress, how does the plant convey the stress signal to other tissues and manage nutrient distribution? This field of study has been largely unexplored. However, the unique interconnected frond structure of Lemna trisulca, along with the use of a divided Petri dish, is very suitable for handling localized stress and investigating the mechanisms of intracellular signaling and nutrient distribution. Research has shown that when the mother leaf experiences localized stress, it releases healthy daughter leaves to minimize collateral damage to the daughter leaves. Conversely, when the daughter leaves face localized stress, the mother leaf chooses to retain them and continues supplying them with nutrients to support their survival. In-depth studies revealed that stressed daughter leaves accumulate Reactive Oxygen Species (ROS), triggering nutrient distribution by sending a distress signal to the mother leaf. This prompts the mother leaf to use Ca2+ as a signaling molecule to deliver nutrients to the daughter leaves. Selective detachment is regulated and triggered by the interaction between Ca2+ and ROS within the mother leaf. When the mother leaf undergoes stress, Ca2+ acts upstream to induce ROS accumulation at the nodes, sending a unidirectional detachment signal to the daughter leaves. This causes ROS accumulation at the daughter leaf nodes, inducing detachment and thereby reducing the collateral damage the daughter leaf could experience due to the mother leaves.