Calendar An icon of a desk calendar. Cancel An icon of a circle with a diagonal line across. Caret An icon of a block arrow pointing to the right. Email An icon of a paper envelope. Facebook An icon of the Facebook "f" mark. Google An icon of the Google "G" mark. Linked In An icon of the Linked In "in" mark. Logout An icon representing logout. Profile An icon that resembles human head and shoulders. Telephone An icon of a traditional telephone receiver. Tick An icon of a tick mark. Is Public An icon of a human eye and eyelashes. Is Not Public An icon of a human eye and eyelashes with a diagonal line through it. Pause Icon A two-lined pause icon for stopping interactions. Quote Mark A opening quote mark. Quote Mark A closing quote mark. Arrow An icon of an arrow. Folder An icon of a paper folder. Breaking An icon of an exclamation mark on a circular background. Camera An icon of a digital camera. Caret An icon of a caret arrow. Clock An icon of a clock face. Close An icon of the an X shape. Close Icon An icon used to represent where to interact to collapse or dismiss a component Comment An icon of a speech bubble. Comments An icon of a speech bubble, denoting user comments. Comments An icon of a speech bubble, denoting user comments. Ellipsis An icon of 3 horizontal dots. Envelope An icon of a paper envelope. Facebook An icon of a facebook f logo. Camera An icon of a digital camera. Home An icon of a house. Instagram An icon of the Instagram logo. LinkedIn An icon of the LinkedIn logo. Magnifying Glass An icon of a magnifying glass. Search Icon A magnifying glass icon that is used to represent the function of searching. Menu An icon of 3 horizontal lines. Hamburger Menu Icon An icon used to represent a collapsed menu. Next An icon of an arrow pointing to the right. Notice An explanation mark centred inside a circle. Previous An icon of an arrow pointing to the left. Rating An icon of a star. Tag An icon of a tag. Twitter An icon of the Twitter logo. Video Camera An icon of a video camera shape. Speech Bubble Icon A icon displaying a speech bubble WhatsApp An icon of the WhatsApp logo. Information An icon of an information logo. Plus A mathematical 'plus' symbol. Duration An icon indicating Time. Success Tick An icon of a green tick. Success Tick Timeout An icon of a greyed out success tick. Loading Spinner An icon of a loading spinner. Facebook Messenger An icon of the facebook messenger app logo. Facebook An icon of a facebook f logo. Facebook Messenger An icon of the Twitter app logo. LinkedIn An icon of the LinkedIn logo. WhatsApp Messenger An icon of the Whatsapp messenger app logo. Email An icon of an mail envelope. Copy link A decentered black square over a white square.

Dundee University’s heart attack breakthrough

Dundee University’s heart attack breakthrough

Scientists at Dundee University may have discovered the key to preventing damage to the heart muscle caused by cardiac arrest.

The research team learned that an enzyme called DHHC5 plays an important role in regulating the force of the contraction of the heart muscle.

However, during a heart attack the enzyme becomes overactive, which can cause permanent damage to the heart muscle. This can cause arrhythmia and even stop the heart from pumping blood around the body effectively.

Dr Will Fuller from the Medical Research Institute at the University of Dundee said: “There are multiple implications arising from our research.

“DHHC5 is a member of a family of enzymes which are implicated in progression of a variety of clinical conditions, including neurological diseases and cancer. So knowing more about how it works could lead to significant developments in those disease areas.

“Secondly, understanding how DHHC5 works raises the possibility that drugs may be able selectively to manipulate its activity. This means we might be able to interfere with the ‘bad’ things this enzyme does, like damaging heart muscle during a heart attack, without affecting the ‘good’ things such as establishing memories in the brain.”

The results of the research, which was supported by the British Heart Foundation, are published in Proceedings of the National Academy of Sciences (PNAS), one of the world’s most-cited and comprehensive multidisciplinary scientific journals.

Professor Jeremy Pearson, associate medical director at the BHF, said: “The research, by showing the precise way in which the DHHC5 enzyme works, offers the potential to design urgently needed new drugs that may block its damaging effect on heart cells after a heart attack that can lead to debilitating heart failure.

“These results are an important first step towards the goal of developing new treatments to prevent damage after a heart attack, but it will require considerably more research to understand whether their promise can be converted into clinical benefit.”