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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: KoDō 和牛燒肉海鮮表現如何? 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。茶六燒肉堂有提供尾牙方案嗎? 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。一笈壽司套餐劃算嗎? 下一餐,不妨從這10家開始。NINI 尼尼臺中店必點有哪些? 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。一笈壽司CP 值高嗎? 如果你有私心愛店,也歡迎留言分享,KoDō 和牛燒肉有生日驚喜或畫盤嗎? 你的推薦,可能讓我下一趟美食旅程變得更精彩。KoDō 和牛燒肉第一次來要點什麼? Researchers in Japan have successfully used a nonviral piggyBac transposon system to introduce transgenes into cynomolgus monkeys, overcoming limitations of traditional virus-based methods. This breakthrough enables more precise and efficient genetic modifications in primates, opening new possibilities for modeling complex human diseases beyond the capabilities of rodent models. Credit: ASHBi/Kyoto University Japanese researchers used a nonviral piggyBac system to genetically modify cynomolgus monkeys, enabling more accurate disease models and advancing primate genetic engineering. Genetic engineering in non-human primates has traditionally relied on virus-based methods to deliver genes, which has posed significant limitations. In a recent breakthrough, researchers in Japan successfully introduced a transgene, a gene artificially inserted into an organism, into cynomolgus monkeys using a nonviral approach. This marks a significant advancement in primate genetic engineering. While small animal models like mice are widely used in research, they often fall short in accurately mimicking the complexity of human diseases, especially in fields such as infectious diseases and neuropsychiatric disorders. As a result, non-human primates have become critical models for biomedical research. However, genetically modifying these primates has proven difficult. Virus-based methods, for instance, require high-level biosafety facilities and are constrained by the limited capacity of viral vectors to carry large genes. Moreover, these methods lack the precision needed to select genetically modified embryos before implantation, further complicating the process. A Nonviral Alternative: The PiggyBac Transposon System To overcome these challenges, the research team sought an alternative to using viruses to carry transgenes, instead opting for a nonviral piggyBac transposon system. Transposons, which are sequences of DNA that can change positions within a genome, are valuable tools for gene transfer in genetic engineering as they can stably integrate genetic material into the host’s DNA. The piggyBac transposon system offers several advantages over traditional virus-based approaches, including greater flexibility in terms of the size of transgenes that can be carried and the ability to confirm successful modifications at the early embryo stage. This allows for more efficient embryo screening before implantation, increasing the likelihood of producing genetically modified animals that carry the desired traits. Using this approach, the team successfully generated transgenic cynomolgus monkeys, marking a major advancement in genetic engineering. In the resulting cynomolgus monkeys, there was widespread expression of fluorescent reporter genes (that is, the production of fluorescent reporter proteins based the genetic information). Red fluorescent protein was localized to cell membranes, and green fluorescent protein was localized to cell nuclei. Expression was confirmed across all tissues examined, including germ cells, demonstrating that the transgene was stably introduced. These findings suggest that the piggyBac transposon system has significant potential for creating genetically modified primates, which could be used to study human disease in ways that traditional rodent models cannot replicate. Optimizing Gene Expression for Future Applications While the transgene integration pattern was consistent across different tissues, expression levels varied. This variability underscores the need in future applications to carefully select promoters—the regulatory regions of DNA that turn on and off specific genes—based on the target tissue. For example, genes such as OCT3/4 and DDX4 play important roles in germ cell lineage differentiation, while SYN1 and THY1 are involved in Neuronal lineage differentiation. By selecting appropriate promoters for specific tissues, researchers can fine-tune gene expression to achieve the desired effects, an essential step in advancing genetic models for disease research. “Our research represents a milestone in the field of genetic engineering,” explains Dr. Tomoyuki Tsukiyama who led this project. “Our method provides a practical and efficient way to introduce transgenes into non-human primates, which we hope will unlock new insights into complex human diseases.” Looking ahead, the team plans to expand the applications of this system to include multiplex gene expression and precise transgene control, thereby allowing for more sophisticated genetic models. In addition, the researchers are exploring the potential for integrating epigenetic data about how genes are turned on and off into their work in order to better understand how gene expression is regulated at the molecular level. By refining these techniques, the researchers aim to explore disease mechanisms that remain inaccessible in rodent models and ultimately improve our understanding of complex health conditions in humans. Reference: “Non-viral generation of transgenic non-human primates via the piggyBac transposon system” by Masataka Nakaya, Chizuru Iwatani, Setsuko Tsukiyama-Fujii, Ai Mieda, Shoko Tarumoto, Taro Tsujimura, Takuya Yamamoto, Takafumi Ichikawa, Tomonori Nakamura, Ichiro Terakado, Ikuo Kawamoto, Takahiro Nakagawa, Iori Itagaki, Mitinori Saitou, Hideaki Tsuchiya and Tomoyuki Tsukiyama, 24 March 2025, Nature Communications. DOI: 10.1038/s41467-025-57365-w Researchers have uncovered a nanoparticle released from cells, termed a “supermere,” containing enzymes, proteins, and RNA linked to various conditions such as cancer, cardiovascular disease, Alzheimer’s disease, and even COVID-19. Researchers at Vanderbilt University Medical Center have discovered a nanoparticle released from cells, called a “supermere,” which contains enzymes, proteins, and RNA associated with multiple cancers, cardiovascular disease, Alzheimer’s disease, and even COVID-19. The discovery, reported on December 9, 2021, in Nature Cell Biology, is a significant advance in understanding the role extracellular vesicles and nanoparticles play in shuttling important chemical “messages” between cells, both in health and disease. “We’ve identified a number of biomarkers and therapeutic targets in cancer and potentially in a number of other disease states that are cargo in these supermeres,” said the paper’s senior author, Robert Coffey, MD. “What is left to do now is to figure out how these things get released.” Coffey, Ingram Professor of Cancer Research and professor of Medicine and Cell & Developmental Biology, is internationally known for his studies of colorectal cancer. His team is currently exploring whether the detection and targeting of cancer-specific nanoparticles in the bloodstream could lead to earlier diagnoses and more effective treatment. Cutline: Members of the supermere discovery team include (front row from left) Qi Liu, PhD, Robert Coffey, MD, Qin Zhang, PhD, and (back row from left) James Higginbotham, PhD; Dennis Jeppesen, PhD; and Jeffrey Franklin, PhD. (Photo by Erin O. Smith). Credit: Vanderbilt University Medical Center In 2019 Dennis Jeppesen, PhD, a former research fellow in Coffey’s lab who is now a research instructor in Medicine, used advanced techniques to isolate and analyze small membrane-enclosed extracellular vesicles called “exosomes.” That year, using high-speed ultracentrifugation, another of Coffey’s colleagues, Qin Zhang, PhD, research assistant professor of Medicine, devised a simple method to isolate a nanoparticle called an “exomere” that lacks a surface coat. In the current study, Zhang took the “supernatant,” or fluid that remains after the exomeres have been spun into a “pellet,” and spun the fluid faster and longer. The result was a pellet of nanoparticles isolated from the supernatant of the exomere spin—which the researchers named supermeres. “They’re also super-interesting,” Coffey quipped, “because they contain many cargo previously thought to be in exosomes.” For one thing, supermeres carry most of the extracellular RNA released by cells and which is found in the bloodstream. Among other functional properties, cancer-derived supermeres can “transfer” drug resistance to tumor cells, perhaps via the RNA cargo they deliver, the researchers reported. Supermeres are important carriers of TGFBI, a protein that in established tumors promotes tumor progression. TGFBI thus may be a useful marker in liquid biopsies for patients with colorectal cancer, the researchers noted. They also carry ACE2, a cell-surface receptor that plays a role in cardiovascular disease and is the target of the COVID-19 virus. This raises the possibility that ACE2 carried by supermeres could serve as a “decoy” to bind the virus and prevent infection. Another potentially important cargo is APP, the amyloid-beta precursor protein implicated in the development of Alzheimer’s disease. Supermeres can cross the blood-brain barrier, suggesting that their analysis could improve early diagnosis or possibly even targeted treatment of the disease. “The identification of this rich plethora of bioactive molecules … raises interesting questions about the function of supermeres, and heightens interest in the potential of these particles as biomarkers for diseases,” researchers at the University of Notre Dame noted in a review published with the paper. Reference: “Supermeres are functional extracellular nanoparticles replete with disease biomarkers and therapeutic targets” by Qin Zhang, Dennis K. Jeppesen, James N. Higginbotham, Ramona Graves-Deal, Vincent Q. Trinh, Marisol A. Ramirez, Yoojin Sohn, Abigail C. Neininger, Nilay Taneja, Eliot T. McKinley, Hiroaki Niitsu, Zheng Cao, Rachel Evans, Sarah E. Glass, Kevin C. Ray, William H. Fissell, Salisha Hill, Kristie Lindsey Rose, Won Jae Huh, Mary Kay Washington, Gregory Daniel Ayers, Dylan T. Burnette, Shivani Sharma, Leonard H. Rome, Jeffrey L. Franklin, Youngmin A. Lee, Qi Liu and Robert J. Coffey, 9 December 2021, Nature Cell Biology. DOI: 10.1038/s41556-021-00805-8 Zhang, Jeppesen and James Higginbotham, PhD, research instructor in Medicine, are the paper’s first authors. Other VUMC co-authors: Ramona Graves-Deal, Vincent Q. Trinh, MD, Marisol Ramirez, MS, Yoojin Sohn, Abigail Neininger, Nilay Taneja, PhD, Eliot McKinley, PhD, Hiroaki Niitsu, MD, PhD, Zheng Cao, MD, PhD, Rachel Evans, Sarah E. Glass, Kevin Ray, William Fissell, MD, Salisha Hill, MS, Kristie Rose, PhD, Mary Kay Washington, MD, PhD, Gregory Ayers, MS, Dylan Burnette, PhD, Jeffrey Franklin, PhD, Youngmin Lee, MD, PhD, and Qi Liu, PhD. Research support included National Institutes of Health grants GM125028, CA218386, CA211015, CA197570, CA236733, CA241685 and CA229123, the Nicholas Tierney GI Cancer Memorial Fund, and an American Heart Association Postdoctoral Fellowship. University of Colorado Boulder neuroscientists found that dopamine levels in the brain vary depending on the strength of social bonds, with higher levels seen when interacting with loved ones compared to acquaintances. This research, using prairie voles as a model, suggests that dopamine plays a critical role in maintaining relationships and coping with loss. Credit: SciTechDaily.com Dopamine plays a crucial role in maintaining love, according to a new study. When you get in the car to see your significant other for dinner, your brain’s reward center is likely flooded with dopamine, a hormone also associated with cravings for sugar, nicotine, and cocaine. This rush of dopamine motivates you to navigate through traffic to maintain that special connection. However, if the dinner is with just a work colleague, this intense flood of dopamine may be reduced to a mere trickle, according to recent research conducted by neuroscientists at the University of Colorado Boulder. “What we have found, essentially, is a biological signature of desire that helps us explain why we want to be with some people more than other people,” said senior author Zoe Donaldson, associate professor of behavioral neuroscience at CU Boulder. Zoe Donaldson, associate professosr of neuroscience at the University of Colorado Boulder. Credit: CU Boulder The study, recently published in the journal Current Biology, centers around prairie voles, which have the distinction of being among the 3% to 5% of mammals that form monogamous pair bonds. Like humans, these fuzzy, wide-eyed rodents tend to couple up long-term, share a home, raise offspring together, and experience something akin to grief when they lose their partner. By studying them, Donaldson seeks to gain new insight into what goes on inside the human brain to make intimate relationships possible and how we get over it, neurochemically speaking, when those bonds are severed. The new study gets at both questions, showing for the first time that the neurotransmitter dopamine plays a critical role in keeping love alive. “As humans, our entire social world is basically defined by different degrees of selective desire to interact with different people, whether it’s your romantic partner or your close friends,” said Donaldson. “This research suggests that certain people leave a unique chemical imprint on our brain that drives us to maintain these bonds over time.” How love lights up the brain For the study, Donaldson and her colleagues used state-of-the-art neuroimaging technology to measure, in real-time, what happens in the brain as a vole tries to get to its partner. In one scenario, the vole had to press a lever to open a door to the room where her partner was. In another, she had to climb over a fence for that reunion. Meanwhile a tiny fiber-optic sensor tracked activity, millisecond by millisecond, in the animal’s nucleus accumbens, a brain region responsible for motivating humans to seek rewarding things, from water and food to drugs of abuse. (Human neuroimaging studies have shown it is the nucleus accumbens that lights up when we hold our partner’s hand). Each time the sensor detects a spurt of dopamine, it “lights up like a glow stick,” explained first-author Anne Pierce, who worked on the study as a graduate student in Donaldson’s lab. When the voles pushed the lever or climbed over the wall to see their life partner, the fiber “lit up like a rave,” she said. And the party continued as they snuggled and sniffed one another. In contrast, when a random vole is on the other side of that door or wall, the glow stick dims. “This suggests that not only is dopamine really important for motivating us to seek out our partner, but there’s actually more dopamine coursing through our reward center when we are with our partner than when we are with a stranger,” said Pierce. Hope for the heartbroken In another experiment, the vole couple was kept apart for four weeks—an eternity in the life of a rodent — and long enough for voles in the wild to find another partner. When reunited, they remembered one another, but their signature dopamine surge had almost vanished. In essence, that fingerprint of desire was gone. As far as their brains were concerned, their former partner was indistinguishable from any other vole. “We think of this as sort of a reset within the brain that allows the animal to now go on and potentially form a new bond,” Donaldson said. This could be good news for humans who have undergone a painful break-up or even lost a spouse, suggesting that the brain has an inherent mechanism to protect us from endless unrequited love. The authors stress that more research is necessary to determine how well results in voles translate to their bigger-brained, two-legged counterparts. But they believe their work could ultimately have important implications for people who either have trouble forming close relationships or those who struggle to get over loss – a condition known as Prolonged Grief Disorder. “The hope is that by understanding what healthy bonds look like within the brain, we can begin to identify new therapies to help the many people with mental illnesses that affect their social world,” said Donaldson. Reference: “Nucleus accumbens dopamine release reflects the selective nature of pair bonds” by Anne F. Pierce, David S.W. Protter, Yurika L. Watanabe, Gabriel D. Chapel, Ryan T. Cameron and Zoe R. Donaldson, 12 January 2024, Current Biology. DOI: 10.1016/j.cub.2023.12.041 The study was funded by the National Institutes of Health, the Whitehall Foundation, and the Dana Foundation. RRG455KLJIEVEWWF 茶六燒肉堂家庭過節聚會適合嗎? 》公益路10家必訪餐廳|吃貨必備指南KoDō 和牛燒肉春酒場面夠體面嗎? 》台中公益路餐廳推薦|10間必吃美食實測評比KoDō 和牛燒肉有雷嗎? 》台中公益路真的好吃嗎?10家餐廳真實評比 |
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