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身為一個熱愛美食、喜歡在城市裡挖掘驚喜的人,臺中公益路一直是我最常出沒的地方之一。這條路可說是「臺中人的美食戰場」,從精緻西餐到創意火鍋,從日式丼飯到義式早午餐,每走幾步,就會有完全不同的特色料理餐廳。 這次我特別花了一整個月,實際造訪了公益路上十間口碑不錯的餐廳。有的是網友熱推的打卡名店,也有隱藏在巷弄裡的小驚喜。我以環境氛圍、口味表現、價格CP值與再訪意願為基準,整理出這篇實測評比。希望能幫正在猶豫去哪裡吃飯的你,找到那一間「吃完會想再來」的餐廳。 評比標準與整理方向
這次我走訪的10家餐廳橫跨不同料理類型,從高質感牛排館到巷弄系早午餐,每一間都有自己獨特的風格。為了讓整體比較更客觀,我依照以下四大面向進行評比,並搭配實際用餐體驗來打分。
整體而言,我希望這份評比不只是「哪家好吃」,而是幫你在不同情境下(約會、家庭聚餐、朋友小聚、商業午餐)都能快速找到合適的選擇。畢竟,美食不只是味覺的滿足,更是一段段與朋友共享的生活記憶。 10間臺中公益路餐廳評比懶人包公益路向來是臺中人聚餐的首選地段,從火鍋、燒肉到中式料理與早午餐,每走幾步就有驚喜。以下是我實際造訪過的10間代表性餐廳清單,橫跨平價、創意、高級各路風格。
一頭牛日式燒肉|炭香濃郁的和牛饗宴,約會聚餐首選
走在公益路上,很難不被 一頭牛日式燒肉 的木質外觀吸引。低調卻不失質感的門面,搭配昏黃燈光與暖色調的內裝,讓人一進門就感受到濃濃的日式職人氛圍。店內空間不大,但桌距規劃得宜,每桌皆設有獨立排煙設備,烤肉時完全不怕滿身油煙味。 餐點特色
一頭牛的靈魂,絕對是他們招牌的「三國和牛拼盤」。 用餐體驗整體節奏掌握得非常好。店員會在你剛想烤下一片肉時貼心遞上夾子、幫忙換烤網,讓人完全不用分心。整場用餐過程就像一場表演,從視覺、嗅覺到味覺都被滿足。 綜合評分
地址:408臺中市南屯區公益路二段162號電話:04-23206800 官網:http://www.marihuana.com.tw/yakiniku/index.html 小結語一頭牛日式燒肉不僅是「吃肉的地方」,更像是一場五感盛宴。從進門那一刻到最後一道甜點,都能感受到他們對細節的用心。 TANG Zhan 湯棧|文青系火鍋代表,麻香湯底與視覺美感並重
在公益路這條美食戰線上,TANG Zhan 湯棧 是讓人一眼就會想走進去的那一種。 餐點特色
湯棧最有名的當然是它的「麻香鍋」。 用餐體驗整體氛圍比一般火鍋店更有質感。 綜合評分
地址:408臺中市南屯區公益路二段248號電話:04-22580617 官網:https://www.facebook.com/TangZhan.tw/ 小結語TANG Zhan 湯棧 把傳統火鍋做出新的樣貌保留臺式鍋物的溫度,又結合現代風格與細節服務,讓吃鍋這件事變得更有品味。 如果你想找一間兼具「好吃、好拍、好放鬆」的火鍋店,湯棧會是公益路上最有風格的選擇之一。 NINI 尼尼臺中店|明亮寬敞的義式早午餐天堂
如果說前兩間是肉食愛好者的天堂,那 NINI 尼尼臺中店 絕對是想放鬆、聊聊天的好地方。餐廳外觀以白色系與大片玻璃窗為主,陽光灑進室內,讓人一踏入就有種度假般的輕盈感。假日早午餐時段特別熱鬧,建議提早訂位。 餐點特色
NINI 的菜單融合義式與臺灣人口味,選擇多樣且份量十足。主打的 松露燉飯 濃郁卻不膩口,米芯保留微Q口感;而 香蒜海鮮義大利麵 則以新鮮白蝦、花枝與淡菜搭配微辣蒜香,口感層次豐富。 用餐體驗店內氣氛輕鬆不拘謹,無論是一個人帶電腦工作、或朋友聚餐,都能找到舒服角落。餐點上桌速度穩定,服務人員態度親切、補水與收盤都非常主動。整體節奏讓人覺得「時間變慢了」,很適合想遠離忙碌日常的人。 綜合評分
地址:40861臺中市南屯區公益路二段18號電話:04-23288498 小結語NINI 尼尼臺中店是一間能讓人放下手機、慢慢吃飯的餐廳。餐點不追求浮誇,而是以「剛剛好」的份量與風味,陪伴每個平凡午後。如果你在找一間能邊吃邊聊天、拍照也漂亮的早午餐店,NINI 會是你在公益路上最不費力的幸福選擇。 加分100%浜中特選昆布鍋物|平價卻用心的湯頭系火鍋,家庭聚餐好選擇
在公益路這條高質感餐廳林立的戰場上,加分100%浜中特選昆布鍋物 走的是截然不同的路線。它沒有浮誇的裝潢、也沒有高價位的套餐,但靠著實在的湯頭與親切的服務,默默吸引許多回頭客。每到用餐時間,總能看到家庭或情侶三兩成群地圍著鍋邊聊天。 餐點特色
主打 北海道浜中昆布湯底,湯頭清澈卻不單薄,越煮越能喝出海藻與柴魚的自然香氣。 用餐體驗整體氛圍偏家庭取向,桌距寬敞、座位舒適,帶小孩來也不覺擁擠。店員態度親切,補湯、收盤都很勤快,給人一種「被照顧著」的安心感。 綜合評分
地址:403臺中市西區公益路288號電話:0910855180 小結語加分100%浜中特選昆布鍋物是一間「不浮誇、但會讓人想再訪」的火鍋店。它不追求豪華擺盤,而是用最簡單的湯頭與新鮮食材,傳遞出家常卻不平凡的溫度。 印月餐廳|中式料理的藝術演繹,宴客與家庭聚會首選
說到臺中公益路的中式料理代表,印月餐廳 絕對是榜上有名。這間開業多年的餐廳以「中菜西吃」的概念聞名,把傳統中式料理以現代手法重新詮釋。從建築外觀到餐具擺設,每個細節都散發著低調的典雅氣息。 餐點特色
印月最令人印象深刻的是他們將傳統中菜融入創意手法。 用餐體驗服務方面完全對得起餐廳的高級定位。從入座、點餐到上菜節奏,都拿捏得恰如其分。每道菜都會有服務人員細心介紹食材與吃法,讓人感受到「被款待」的尊榮感。 綜合評分
地址:408臺中市南屯區公益路二段818號電話:0422511155 小結語印月餐廳是一間「不只吃飯,更像品味生活」的地方。 KoDō 和牛燒肉|極致職人精神,專為儀式感與頂級味覺而生
若要形容 KoDō 和牛燒肉 的用餐體驗,一句話足以總結——「像在欣賞一場關於肉的表演」。 餐點特色
這裡主打 日本A5和牛冷藏肉,以「精切厚燒」的方式呈現。 用餐體驗KoDō 的最大特色是「儀式感」。 綜合評分
地址:403臺中市西區公益路260號電話:0423220312 官網:https://www.facebook.com/kodo2018/ 小結語KoDō 和牛燒肉不是日常餐廳,而是一場體驗。 永心鳳茶|在茶香裡用餐的優雅時光,臺味早午餐的新詮釋
走進 永心鳳茶公益店,彷彿進入一間有氣質的茶館。 餐點特色
永心鳳茶的餐點結合中式靈魂與西式擺盤,無論是「炸雞腿飯」還是「紅玉紅茶拿鐵」,都能讓人感受到熟悉卻不平凡的味道。 用餐體驗店內服務人員態度溫和,對茶品介紹詳盡。上餐節奏剛好,不急不徐。 綜合評分
地址:40360臺中市西區公益路68號三樓(勤美誠品)電話:0423221118 小結語永心鳳茶讓人重新定義「臺味」。 三希樓|老饕級江浙功夫菜,穩重又帶人情味的中式饗宴
位於公益路上的 三希樓 是許多臺中老饕的口袋名單。 餐點特色
三希樓的菜色以 江浙與港式料理 為主,兼顧傳統與現代風味。 用餐體驗三希樓的服務給人一種老派但貼心的感覺。 綜合評分
地址:408臺中市南屯區公益路二段95號電話:0423202322 官網:https://www.sanxilou.com.tw/ 小結語三希樓是一間「吃得出功夫」的餐廳。 一笈壽司|低調奢華的無菜單日料,職人手藝詮釋旬味極致
在熱鬧的公益路上,一笈壽司 低調得幾乎不顯眼。 餐點特色
一笈壽司採 Omakase(無菜單料理) 形式,每一餐都由主廚根據當日食材設計。 用餐體驗整場用餐約90分鐘,節奏緩慢但沉穩。 綜合評分
地址:408臺中市南屯區公益路二段25號電話:0423206368 官網:https://www.facebook.com/YIJI.sushi/ 小結語一笈壽司是一間真正讓人「放慢呼吸」的餐廳。 茶六燒肉堂|人氣爆棚的和牛燒肉聖地,肉香與幸福感同時滿分
若要票選公益路上「最難訂位」的餐廳,茶六燒肉堂 絕對名列前茅。 餐點特色
茶六主打 和牛燒肉套餐,價格約落在 $700–$1000 間,份量與品質兼具。 用餐體驗茶六的服務效率相當高。店員親切、換網勤快、補水速度快,整場用餐流程流暢無壓力。 綜合評分
地址:403臺中市西區公益路268號電話:0423281167 官網:https://inline.app/booking/-L93VSXuz8o86ahWDRg0:inline-live-karuizawa/-LUYUEIOYwa7GCUpAFWA 小結語茶六燒肉堂用「穩定品質+輕奢氛圍」抓住了臺中年輕族群的心。 吃完10家公益路餐廳後的心得與結語吃完這十家餐廳後,臺中公益路不只是一條美食街,而是一段生活風景線。 有的餐廳講究細膩與儀式感,像 一頭牛日式燒肉 與 一笈壽司,讓人感受到食材最純粹的美好 有的則以親切與溫度打動人心,像 加分昆布鍋物、永心鳳茶,讓人明白吃飯不只是為了飽足,而是一種被照顧的幸福。 而像茶六燒肉堂、TANG Zhan 湯棧 這類人氣名店,則用穩定的品質與熱絡的氛圍,成為許多臺中人心中「想吃肉就去那裡」的代名詞。 這十家店,構成了公益路最動人的縮影 有華麗的,也有溫柔的;有傳統的,也有創新的。 每一家都在自己的風格裡發光,讓人吃到的不只是料理,而是一種生活的溫度與節奏。 對我而言,這不僅是一場美食旅程,更是一趟關於「臺中味道」的回憶之旅。 FAQ:關於臺中公益路美食常見問題Q1:公益路哪一區的餐廳最集中? Q2:需要提前訂位嗎? 最後的話若要用一句話形容這趟美食之旅,我會說: 永心鳳茶適合請客嗎? 如果你也和我一樣喜歡用味蕾探索一座城市,那就把這篇公益路美食攻略收藏起來吧。加分100%浜中特選昆布鍋物用餐時間會不會太短? 無論是約會、慶生、家庭聚餐,或只是想犒賞一下辛苦的自己——這條路上永遠會有一間剛剛好的餐廳在等你。茶六燒肉堂值得推薦嗎? 下一餐,不妨從這10家開始。TANG Zhan 湯棧假日會大排長龍嗎? 打開手機、約上朋友,讓公益路成為你生活裡最容易抵達的小確幸。NINI 尼尼臺中店員工聚會夠氣派嗎? 如果你有私心愛店,也歡迎留言分享,KoDō 和牛燒肉適合多人團聚嗎? 你的推薦,可能讓我下一趟美食旅程變得更精彩。三希樓飲料值得加點嗎? Researchers have discovered that Chromosphaera perkinsii, an ancient single-celled organism, can form multicellular structures resembling early animal embryos, suggesting that the genetic mechanisms behind egg cell development and embryonic processes may have existed well before the first animals appeared. (Artist’s concept of a human egg cell). Scientists have observed a type of cell division in a prehistoric unicellular organism that resembles the embryonic development seen in animal embryos, hinting that embryonic processes may have existed before animals evolved. Chromosphaera perkeinsii is a single-celled organism first identified in 2017 within marine sediments near Hawaii. Traces of its existence date back over a billion years, predating the earliest animals. Researchers from the University of Geneva (UNIGE) have observed that this species forms multicellular structures that bear striking similarities to animal embryos. These observations suggest that the genetic programs responsible for embryonic development were already present before the emergence of animal life, or that C. perkinsii evolved independently to develop similar processes. Nature would therefore have possessed the genetic tools to “create eggs” long before it “invented chickens”. This study is published in the journal Nature. The first life forms to appear on Earth were unicellular, i.e. composed of a single cell, such as yeast or bacteria. Later, animals – multicellular organisms – evolved, developing from a single cell, the egg cell, to form complex beings. This embryonic development follows precise stages that are remarkably similar between animal species and could date back to a period well before the appearance of animals. However, the transition from unicellular species to multicellular organisms is still very poorly understood. Research on Chromosphaera perkinsii Recently appointed as an assistant professor at the Department of Biochemistry in the UNIGE Faculty of Science, and formerly an SNSF Ambizione researcher at EPFL, Omaya Dudin and his team have focused on Chromosphaera perkinsii, or C. perkinsii, an ancestral species of protist. This unicellular organism separated from the animal evolutionary line more than a billion years ago, offering valuable insight into the mechanisms that may have led to the transition to multicellularity. Images of the multicellular development of the ichthyosporean Chromosphaera perkinsii, a close cousin of animals. In red, the membranes and in blue the nuclei with their DNA. The image was obtained using expansion microscopy. Credit: O. Dudin – UNIGE By observing C. perkinsii, the scientists discovered that these cells, once they have reached their maximum size, divide without growing any further, forming multicellular colonies resembling the early stages of animal embryonic development. Unprecedentedly, these colonies persist for around a third of their life cycle and comprise at least two distinct cell types, a surprising phenomenon for this type of organism. Similarities with Animal Embryos ‘‘Although C. perkinsii is a unicellular species, this behavior shows that multicellular coordination and differentiation processes are already present in the species, well before the first animals appeared on Earth’’, explains Omaya Dudin, who led this research. Even more surprisingly, the way these cells divide and the three-dimensional structure they adopt are strikingly reminiscent of the early stages of embryonic development in animals. In collaboration with Dr. John Burns (Bigelow Laboratory for Ocean Sciences), analysis of the genetic activity within these colonies revealed intriguing similarities with that observed in animal embryos, suggesting that the genetic programs governing complex multicellular development were already present over a billion years ago. Marine Olivetta, laboratory technician at the Department of Biochemistry in the UNIGE Faculty of Science and first author of the study, explains: “It’s fascinating, a species discovered very recently allows us to go back in time more than a billion years”. In fact, the study shows that either the principle of embryonic development existed before animals, or multicellular development mechanisms evolved separately in C. perkinsii. This discovery could also shed new light on a long-standing scientific debate concerning 600 million-year-old fossils that resemble embryos, and could challenge certain traditional conceptions of multicellularity. Reference: “A multicellular developmental program in a close animal relative” by Marine Olivetta, Chandni Bhickta, Nicolas Chiaruttini, John Burns and Omaya Dudin, 6 November 2024, Nature. DOI: 10.1038/s41586-024-08115-3 Researchers from Japan, discover mitochondrial transfer from cancer cells to immune cells and metabolic reprogramming of the tumor microenvironment as a key immune evasion strategy. Targeting mitochondrial transfer can help improve the efficacy of immunotherapy in unresponsive patients. Credit: izhongweining from Openverse Researchers identify mitochondrial transfer between cancer and immune cells as a crucial mechanism for immune evasion. The immune system is essential for identifying and eliminating cancer cells. Cancer immunotherapy enhances this process by training immune cells to recognize and attack tumors. However, many cancers develop mechanisms to evade immune detection, leading to resistance to treatment. Understanding the molecular basis of this immune evasion is crucial for improving therapeutic strategies. The tumor microenvironment (TME)—the area surrounding a tumor—plays a pivotal role in interactions between cancer and immune cells. Cancer cells can manipulate the TME to suppress tumor-infiltrating lymphocytes (TILs), the immune cells responsible for attacking tumors. Mitochondria, often called the “powerhouse of the cell,” generate energy for various cellular functions and play a key role in the metabolic reprogramming of both cancer cells and TILs. However, the exact mechanisms of mitochondrial dysfunction and its impact on the TME remain poorly understood. New Research on Mitochondrial Dysfunction in Cancer To address this knowledge gap, a team of researchers led by Professor Yosuke Togashi from Okayama University, Japan, has uncovered novel insights into mitochondrial dysfunction in cancer immune evasion. Working alongside Tatsuya Nishi and Tomofumi Watanabe from Okayama University, as well as Hideki Ikeda, Katsushige Kawase, and Masahito Kawazu from the Chiba Cancer Center Research Institute, the team identified mitochondrial transfer as a key mechanism of immune evasion. This study was published online in Nature on January 22, 2025. Prof. Togashi explains, “We have discovered mitochondrial transfer as one of the key mechanisms of immune evasion. Our research adds a new dimension to the understanding of how tumors resist immune responses, potentially leading to the development of more comprehensive and tailored approaches in treating different cancers.” Mitochondria carry their own DNA (mtDNA), which encodes proteins crucial for energy production and transfer. However, mtDNA is prone to damage, and mutations in mtDNA can promote tumor growth and metastasis. In this study, the researchers examined TILs from patients with cancer and found that they contained the same mtDNA mutations as the cancer cells. Further analysis revealed that these mutations were linked to abnormal mitochondrial structures and dysfunction in TILs. Using a fluorescent marker, the researchers tracked mitochondrial movement between cancer cells and T cells. They found that mitochondria were transferred via direct cell-to-cell connections called tunneling nanotubes, as well as through extracellular vesicles. Once inside T cells, the cancer-derived mitochondria gradually replaced the original T cell mitochondria, leading to a state called ‘homoplasmy,’ where all mtDNA copies in the cell are identical. How Cancer Cells Protect Transferred Mitochondria Normally, damaged mitochondria in TILs are removed through a process called mitophagy. However, mitochondria transferred from cancer cells appeared to resist this degradation. The researchers discovered that mitophagy-inhibiting factors were co-transferred with the mitochondria, preventing their breakdown. As a result, TILs experienced mitochondrial dysfunction, leading to reduced cell division, metabolic changes, increased oxidative stress, and impaired immune response. In mouse models, these dysfunctional TILs also showed resistance to immune checkpoint inhibitors, a type of immunotherapy. By identifying mitochondrial transfer as a novel immune evasion mechanism, this study opens new possibilities for improving cancer treatment. Blocking mitochondrial transfer could enhance immunotherapy response, particularly in patients with treatment-resistant cancers. Cancer therapies often involve high costs and significant side effects, particularly when they are ineffective. Enhancing the success of immunotherapy by inhibiting mitochondrial transfer could reduce the burden of cancer and improve patient outcomes. Prof. Togashi concludes by saying, “Existing cancer treatments are not universally effective, and there is a pressing need for new therapies that can overcome resistance mechanisms. Developing drugs that inhibit mitochondrial transfer between cancer cells and immune cells may enhance the efficacy of immunotherapies, thereby providing personalized treatment options for patients with cancers that are resistant to current therapies.” This discovery offers exciting new insights into cancer biology and could pave the way for more effective therapies in the future. Reference: “Immune evasion through mitochondrial transfer in the tumour microenvironment” by Hideki Ikeda, Katsushige Kawase, Tatsuya Nishi, Tomofumi Watanabe, Keizo Takenaga, Takashi Inozume, Takamasa Ishino, Sho Aki, Jason Lin, Shusuke Kawashima, Joji Nagasaki, Youki Ueda, Shinichiro Suzuki, Hideki Makinoshima, Makiko Itami, Yuki Nakamura, Yasutoshi Tatsumi, Yusuke Suenaga, Takao Morinaga, Akiko Honobe-Tabuchi, Takehiro Ohnuma, Tatsuyoshi Kawamura, Yoshiyasu Umeda, Yasuhiro Nakamura, Yukiko Kiniwa, Eiki Ichihara, Hidetoshi Hayashi, Jun-ichiro Ikeda, Toyoyuki Hanazawa, Shinichi Toyooka, Hiroyuki Mano, Takuji Suzuki, Tsuyoshi Osawa, Masahito Kawazu and Yosuke Togashi, 22 January 2025, Nature. DOI: 10.1038/s41586-024-08439-0 Funding: Grants-in-Aid for Scientific Research, Challenging Exploratory Research, Grant-in-Aid for Research Fellow from the Japan Society for the Promotion of Science, Project for Cancer Research and Therapeutic Evolution, Practical Research for Innovative Cancer Control, Core Research for Evolutional Science and Technology, Practical Research Project for Rare/Intractable Diseases, Research Program for Hepatitis from the Japan Agency for Medical Research and Development, Fusion Oriented Research for disruptive Science and Technology, ACT-X from the Japan Science and Technology Agency, National Cancer Center Research and Development Fund, Chiba Prefecture Research Grant, Takeda Science Foundation, Naito Foundation, Mochida Memorial Foundation, MSD Life Science Foundation, GSK Japan foundation, Research Grant of the Princess Takamatsu Cancer Research Fund, Kowa Life Science Foundation, Kato Memorial Bioscience Foundation, Inamori Foundation, Astellas Foundation for Research on Metabolic Disorders, Suzuken Memorial Foundation, SGH Foundation, Sumitomo Foundation Grant for Basic Science Research Projects, Terumo Life Science Foundation, Chugai Foundation for Innovative Drug Discovery Science, The Ono Pharmaceutical Foundation for Oncology, Immunology, and Neurology, Kobayashi Foundation for Cancer Research, Taiju Life Social Welfare Foundation, 2023 Healthcare Innovation Research Grant established with donations from T. Togawa, Sequencing and bioinformatics analyses were performed on institutional computing resources that included hardware provided by NVIDIA The research was conducted with Mongolian gerbils, rodents that form lasting pair bonds and raise their pups together. The work showed the nuanced effects of testosterone, depending on context. It also revealed how testosterone influences the neural activity of oxytocin cells, the so-called love hormone associated with social bonding. Credit: Aubrey Kelly The Hormone Seems To Help Animals Quickly Switch Between Prosocial and Antisocial Behaviors According to a recent animal study, testosterone may encourage males to be sociable and friendlier. The research on Mongolian gerbils was conducted by Emory University neuroscientists and was recently published in the journal Proceedings of the Royal Society B. “For what we believe is the first time, we’ve demonstrated that testosterone can directly promote nonsexual, prosocial behavior, in addition to aggression, in the same individual,” says Aubrey Kelly, Emory assistant professor of psychology and first author of the study. “It’s surprising because normally we think of testosterone as increasing sexual behaviors and aggression. But we’ve shown that it can have more nuanced effects, depending on the social context.” Additionally, the research demonstrated how testosterone affects the brain activity of oxytocin cells, the so-called “love hormone” linked to social bonding. Richmond Thompson, a neuroscientist at Emory University’s Oxford College, is one of the study’s co-authors. Recent research conducted in Kelly’s lab on rodent experimental models has focused on the brain effects of oxytocin. Thompson’s group explores the neural effects of steroids in fish. Both researchers are attempting to understand how hormones function in the brain to enable an animal to quickly alter its behavior based on the social situation. Kelly and Thompson live together as a married couple in addition to sharing this research interest. “The idea for this paper was borne out of us talking together over a glass of wine,” Kelly says. “It blends our two research worlds.” The majority of human studies demonstrate that testosterone increases aggressive behavior. Kelly and Thompson questioned if testosterone would potentially, simultaneously with its ability to promote hostility against intruders, also reduce prosocial behaviors. They also hypothesized that it may accomplish something more radical: it would actually boost positive social reactions in situations when behaving prosocially is appropriate. The Kelly group performed research on Mongolian gerbils, rodents that create long-lasting pair bonds and nurture their offspring together, to answer this question. While males may become violent during mating and in defense of their territory, they also display cuddling and protective behavior toward their offspring once a female gets pregnant. In one experiment, a male gerbil was introduced to a female gerbil. After they developed a pair connection and the female got pregnant, the males displayed the typical cuddling behaviors toward their partners. The male individuals were subsequently given testosterone injections by the researchers. They hypothesized that the subsequent acute rise in a male’s testosterone level would reduce his cuddling behaviors since testosterone is generally an antisocial molecule. Testosterone Enhances Prosocial Responses “Instead, we were surprised that a male gerbil became even more cuddly and prosocial with his partner,” Kelly says. “He became like ‘super partner.’” In a follow-up experiment a week later, the researchers conducted a resident-intruder test. The females were removed from the cages so that each male gerbil that had previously received a testosterone injection was alone in his home cage. An unknown male was then introduced into the cage. “Normally, a male would chase another male that came into its cage, or try to avoid it,” Kelly says. “Instead, the resident males that had previously been injected with testosterone were more friendly to the intruder.” The friendly behavior abruptly changed, however, when the original male subjects were given another injection of testosterone. They then began exhibiting normal chasing and/or avoidance behaviors with the intruder. “It was like they suddenly woke up and realized they weren’t supposed to be friendly in that context,” Kelly says. The researchers theorize that because the male subjects experienced a surge in testosterone while they were with their partners, it not only rapidly increased positive social responses toward them but also primed the males to act more prosocially in the future, even when the context changed and they were in the presence of another male. However, the second testosterone injection then rapidly prompted them to switch their behavior to become more aggressive, as appropriate to the context of a male intruder. Testosterone’s Role in Context-Appropriate Behavior “It appears that testosterone enhances context-appropriate behavior,” Kelly says. “It seems to play a role in amplifying the tendency to be cuddly and protective or aggressive.” The laboratory experiments, in a sense, slowed down what the males might experience almost simultaneously in the wild. In their natural habitat, Kelly explains, mating with a partner elevates testosterone, which primes them to act cuddly in the moment and in the near future while living with their partner, even if the testosterone levels decline. If a rival entered its burrow the gerbil would likely experience another surge of testosterone that would immediately help adjust his behavior so he can fend off the rival and protect his pups. Testosterone then appears to help animals rapidly pivot between prosocial and antisocial responses as the social world changes. Interaction Between Testosterone and Oxytocin The current study also looked at how testosterone and oxytocin interact biologically. The results showed that the male subjects receiving injections of testosterone exhibited more oxytocin activity in their brains during interactions with a partner compared to males that did not receive the injections. “We know that systems of oxytocin and testosterone overlap in the brain but we don’t really understand why,” Kelly says. “Taken together, our results suggest that one of the reasons for this overlap may be so they can work together to promote prosocial behavior.” Rather than just flipping an “on” or “off” button to modulate behaviors, hormones seem to play a more nuanced role, Kelly says. “It‘s like a complicated dashboard where one dial may need to move up a bit while another one moves down.” Implications for Understanding Human Social Behavior Human behaviors are far more complex than those of Mongolian gerbils, but the researchers hope that their findings provide a basis for complementary studies on other species, including humans. “Our hormones are the same, and the parts of the brain they act upon are even the same,” Thompson says. “So, learning how hormones like testosterone help other animals adjust to rapidly changing social contexts will not only help us understand the biological nuts and bolts that affect their behavior but also predict and ultimately understand how the same molecules in human brains help shape our own responses to the social world around us.” Reference: “Beyond sex and aggression: testosterone rapidly matches behavioural responses to social context and tries to predict the future” by Aubrey M. Kelly, Jose Antonio Gonzalez Abreu and Richmond R. Thompson, 8 June 2022, Proceedings of the Royal Society B Biological Sciences. DOI: 10.1098/rspb.2022.0453 The study was funded by the National Science Foundation. RRG455KLJIEVEWWF NINI 尼尼台中店適合多人團聚嗎? 》台中公益路吃起來|精選10家餐廳推薦印月餐廳值得推薦嗎? 》公益路聚餐必去名單|10家適合各種場合一笈壽司大型聚餐空間夠不夠? 》台中公益路美食地圖|10家餐廳實測心得 |
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