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Interactions Between The ? And ? Subunits Of The DHPR - A Missing Link In Skeletal Muscle Excitation-contraction Coupling And A Role In Sarcopenia
Funder
National Health and Medical Research Council
Funding Amount
$690,832.00
Summary
Calcium signaling is disrupted in muscle diseases, including muscle weakness in the elderly. This is a significant problem as all mobility depends on calcium signaling and its disruption can cause serious disability and death. To alleviate defective calcium signaling, the underlying molecular machinery must be fully understood, yet we have only a broad outline of the processes. We will address this problem to provide a platform for alleviating age-related muscle weakness.
Communication Between Calcium Ion Channels In Skeletal Muscle Excitation-contraction Coupling
Funder
National Health and Medical Research Council
Funding Amount
$603,100.00
Summary
Ageing, injury, drugs or genetic defects cause muscle weakness, prevent exercise, compromise life style and contribute to poor health and osteoporosis. In order to move signals travel from our brain to muscles, where one calcium ion channel detects the signal and tells a second calcium channel to open and release calcium ions to initiate contraction. The project will pave the way for developing drugs to help with muscle disorders by trageting the site of interaction between the channels.
Regulation Of Calcium Release Channels (RyR2) In Healthy And Failing Hearts
Funder
National Health and Medical Research Council
Funding Amount
$337,632.00
Summary
In striated muscle, the sarcoplasmic reticulum (SR) is the calcium store from which calcium release through ryanodine receptors (RyR2) is the key determinate of muscle force. We will develop an understanding of the complex functional changes in RyR2 that underlie adaptation of the heart to physiological stress (exercise) and functional changes associated with mal-adaptation in heart failure.
Characteristics Of Splice Variants Of The Skeletal Muscle Ryanodine Receptor: Implications For Myotonic Dystrophy
Funder
National Health and Medical Research Council
Funding Amount
$258,000.00
Summary
The project is to address some of the basic molecular changes that occur in skeletal muscle during development and in myotonic dystrophy. Myotonic dystrophy is a significant health issue since it is the most common adult muscular dystrophy, with an occurrence of ~1 in 7000. The results will provide much needed information about the membrane-associated molecular mechanisms that regulate muscle contraction and may provide a basis for drug design and treatment of myotonic dystrophy. Respiration and ....The project is to address some of the basic molecular changes that occur in skeletal muscle during development and in myotonic dystrophy. Myotonic dystrophy is a significant health issue since it is the most common adult muscular dystrophy, with an occurrence of ~1 in 7000. The results will provide much needed information about the membrane-associated molecular mechanisms that regulate muscle contraction and may provide a basis for drug design and treatment of myotonic dystrophy. Respiration and locomotion depend on the release of calcium ions from stores inside muscle cells. Ryanodine receptor calcium channels regulate calcium release from the stores. The essential nature of ryanodine receptors is underlined by death at or before birth when ryanodine receptor expression is defective. In addition genetic defects in the ryanodine receptor cause cardiac arrhythmias, malignant hyperthermia and central core disease. Ryanodine receptor function is compromised in heart failure and fatigue. The essential role of ryanodine receptors makes them a potential therapeutic target, but they are not used in this way because of our limited knowledge of the protein. Myotonic dystrophy is an autosomal dominant multi-system disorder, in which an expansion of non-coding DNA leads to changes in expression of several different proteins. Although the genetic basis of myotonic dystrophy is now reasonably well understood, the contribution of molecular changes in the affected proteins to the myopathy has not been investigated. Our group has recently discovered that the juvenile form of the ryanodine receptor protein is highly expressed in adults suffering from myotonic dystrophy. By discovering more about the properties of the juvenile isoform, we will understand more about the basic mechanisms of ryanodine receptor function in developing muscle and in myotonic dystrophy and be able to design drugs to specifically modify ryanodine receptor activity.Read moreRead less
DHPR ? Subunit Binding To A Variably Spliced Region Of RyR1: A Role In EC Coupling And Myotonic Dystrophy
Funder
National Health and Medical Research Council
Funding Amount
$555,892.00
Summary
We have uncovered a communication pathway between two ion channel molecules in muscle cells that underlies human movement. The pathway is critical in normal mobility and is disrupted in myotonic dystrophy. We will study the molecular components of this pathway to understand normal body function and abnormal function in mytotonic dystrophy. The work will facilitate the design of drugs to relieve the mytotonic dystrophy myopathy and form new and much needed class of specific muscle relaxants.
Aberrant Behaviour Of Cardiac Calcium Release Channels Induced By Ryanodine Receptor Peptide Probes
Funder
National Health and Medical Research Council
Funding Amount
$315,375.00
Summary
Contraction of heart muscle is regulated by the release of calcium ions from an intracellular store known as the sarcoplasmic reticulum. Calcium is released from this store to trigger contraction and then taken up again to let the heart muscle relax. Calcium flows out from the store through a specialised type of ion channel protein known as the ryanodine receptor. Recently, genetic studies have indicted that some forms of sudden cardiac death are due to mutations in the ryanodine receptor in the ....Contraction of heart muscle is regulated by the release of calcium ions from an intracellular store known as the sarcoplasmic reticulum. Calcium is released from this store to trigger contraction and then taken up again to let the heart muscle relax. Calcium flows out from the store through a specialised type of ion channel protein known as the ryanodine receptor. Recently, genetic studies have indicted that some forms of sudden cardiac death are due to mutations in the ryanodine receptor in the heart of susceptible individuals. However, nothing is currently known about how such mutations affect the function of the ryanodine receptor or how this can cause the abnormal heart beating that leads to sudden cardiac death. This project will investigate the normal functioning of the ryanodine receptor and what aberrations occur with the different mutations. This could lead to better treatment of individuals susceptible to this type of sudden cardiac death. The effectiveness of one type of drug in preventing aberrant channel behaviour will also be examined.Read moreRead less
Glutathione Transferase-derived Compounds As Therapeutic Agents
Funder
National Health and Medical Research Council
Funding Amount
$418,516.00
Summary
Inhibition of cardiac calcium ion channels may be an effective new way of improving heart performance in patients with heart failure. This project will investigate how a glutathione transferase enzyme inhibits calcium ion channels in the heart and if small fragments of a muscle specific glutathione transferase can be used to specifically modify cardiac ryanodine receptor function. These fragments will provide the basis for the development of a new therapeutic approach.
Structure Determination Of The Mammalian Ryanodine Receptor
Funder
National Health and Medical Research Council
Funding Amount
$377,397.00
Summary
Heart failure is the leading cause of death worldwide. We will determine the structure of the ryanodine receptor, a calcium channel involved in initiating contraction of cardiac and skeletal muscle. Detailed insights into the function of the ryanodine receptor will result from this work. An atomic structure of the cardiac ryanodine receptor will assist in the development of improved ryanodine receptor inhibitors to prevent and treat congestive heart failure.