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1.
J Biol Chem ; 285(51): 40282-93, 2010 Dec 17.
Article in English | MEDLINE | ID: mdl-20947500

ABSTRACT

The results of our in vitro experiments indicate that exposing cultured human aortic smooth muscle cells and dermal fibroblasts to 39 to 41 °C induces a significant up-regulation in the net deposition of elastic fibers, but not of collagen I or fibronectin, and also decreases the deposition of chondroitin sulfate-containing moieties. We further demonstrate that mild hyperthermia also rectifies the insufficient elastogenesis notable in cultures of fibroblasts derived from the stretch-marked skin of adult patients and in cultures of dermal fibroblasts from children with Costello syndrome, which is characterized by the accumulation of chondroitin 6-sulfate glycosaminoglycans that induce shedding and inactivation of the 67-kDa elastin-binding protein. We have previously established that this protein serves as a reusable chaperone for tropoelastin and that its recycling is essential for the normal deposition of elastic fibers. We now report that hyperthermia not only inhibits deposition of chondroitin 6-sulfate moieties and the consequent preservation of elastin-binding protein molecules but also induces their faster recycling. This, in turn, triggers a more efficient preservation of tropoelastin, enhancement of its secretion and extracellular assembly into elastic fibers. The presented results encourage using mild hyperthermia to restore elastic fiber production in damaged adult skin and to enhance elastogenesis in children with genetic elastinopathies.


Subject(s)
Costello Syndrome/metabolism , Elastic Tissue/metabolism , Fibroblasts/metabolism , Heat-Shock Response , Receptors, Cell Surface/metabolism , Tropoelastin/metabolism , Adult , Cells, Cultured , Child , Child, Preschool , Costello Syndrome/pathology , Elastic Tissue/pathology , Fibroblasts/pathology , Glycosaminoglycans , Humans , Infant , Male
2.
Physiother Theory Pract ; 33(2): 124-130, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28095102

ABSTRACT

Hip extension strengthening exercises which maximize gluteus maximus contributions and minimize hamstring influences may be beneficial for persons with hip pain. This study's aim was to compare muscle activation of the gluteus maximus and hamstrings from healthy subjects during a supine resisted hip extension exercise versus supine unilateral bridge to neutral. Surface electromyographic (EMG) signals were obtained from the right gluteus maximus and hamstrings in 13 healthy male and 13 healthy female subjects. Maximum voluntary isometric contractions (MVICs) were collected to normalize data and permit meaningful comparisons across muscles. Peak median activation of the gluteus maximus was 33.8% MVIC for the bridge and 34.7% MVIC for the hip extension exercise, whereas peak median recruitment for hamstrings was 28.4% MVIC for the bridge and 51% MVIC for the hip extension exercise. The gluteus maximus to hamstrings ratio was compared between the two exercises using the Wilcoxon signed-ranks test (α = 0.05). The ratio (p = 0.014) was greater in the supine unilateral bridge (median = 111.3%) than supine hip extension exercise (median = 59.2%), suggesting a reduction of hamstring recruitment in the unilateral bridge to neutral compared to the supine resisted hip extension exercise. The supine hip extension exercise demonstrated higher EMG activity of hamstrings in comparison with supine unilateral bridge and, therefore, may be less appropriate in subjects who need to increase gluteus maximus activation.


Subject(s)
Electromyography , Exercise Therapy/methods , Hamstring Muscles/physiology , Hip Joint/physiology , Muscle Contraction , Muscle Strength , Patient Positioning/methods , Supine Position , Adult , Female , Healthy Volunteers , Humans , Male , Young Adult
3.
Physiother Theory Pract ; 31(6): 418-27, 2015.
Article in English | MEDLINE | ID: mdl-25671354

ABSTRACT

The aim of this study was to compare the magnitude of selective core muscle activation during supine bridging to neutral exercises (three on a stable and three on an unstable surface). Surface EMG analysis was performed on the lumbar multifidus, gluteus medius, gluteus maximus, and hamstrings from 13 male and 13 female subjects. Lumbar multifidus recruitment was not influenced by exercise or condition and ranged between 29.2 and 35.9% of maximum voluntary isometric contraction (MVIC). Peak gluteus medius activation (42.0% MVIC) occurred in unstable single-leg bridge. Maximum recruitment of gluteus maximus (32.6% MVIC) appeared during stable single-leg bridge. Peak hamstring activation (59.6% MVIC) occurred during stable double-leg hamstring curl. Regardless of condition, hamstrings demonstrated high (51.9-59.6% MVIC) muscle recruitment during double-leg hamstring curls compared with the single-leg bridge or double-leg bridge. Various supine bridging to neutral exercises activated the hamstrings at levels conducive to strengthening, whereas recruitment of lumbar multifidus, gluteus medius, and gluteus maximus promoted endurance training. Clinically, we were unable to conclude the unstable support surface was preferable to the stable surface for boosting muscle recruitment of spine stabilizers, gluteals, and hamstring muscles during supine bridge to neutral position.


Subject(s)
Back Muscles/physiology , Exercise Therapy/methods , Isometric Contraction , Muscle, Skeletal/physiology , Patient Positioning/methods , Postural Balance , Supine Position , Adult , Biomechanical Phenomena , Buttocks , Electromyography , Female , Healthy Volunteers , Humans , Lower Extremity , Male , Young Adult
4.
J Bacteriol ; 184(8): 2314-8, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11914366

ABSTRACT

The S-box transcription termination control system, first identified in Bacillus subtilis, is used for regulation of gene expression in response to methionine availability. The presence of the S-box motif provided the first indication that the ykrTS and ykrWXYZ genes could play a role in recycling of 5'-methylthioadenosine, a by-product of polyamine biosynthesis that can be converted to methionine. In this study we demonstrate a role for the ykrTS and ykrWXYZ gene products in this pathway.


Subject(s)
Bacillus subtilis/genetics , Deoxyadenosines/metabolism , Genes, Bacterial/physiology , Methionine/biosynthesis , Thionucleosides/metabolism , Bacillus subtilis/metabolism , Base Sequence , Gene Expression Regulation, Bacterial , Molecular Sequence Data
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