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1.
Eur J Appl Physiol ; 116(1): 129-44, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26349745

ABSTRACT

PURPOSE: We investigated the effects of moderate-intensity training at low and high altitude on VO2 and QaO2 kinetics and on myosin heavy-chain expression (MyHC) in seven women (36.3 yy ± 7.1; 65.8 kg ± 11.7; 165 cm ± 8) who participated in two 12- to 14-day trekking expeditions at low (598 m) and high altitude (4132 m) separated by 4 months of recovery. METHODS: Breath-by-breath VO2 and beat-by-beat QaO2 at the onset of moderate-intensity cycling exercise and energy cost of walking (Cw) were assessed before and after trekking. MyHC expression of vastus lateralis was evaluated before and after low-altitude and after high-altitude trekking; muscle fiber high-resolution respirography was performed at the beginning of the study and after high-altitude trekking. RESULTS: Mean response time of VO2 kinetics was faster (P = 0.002 and P = 0.001) and oxygen deficit was smaller (P = 0.001 and P = 0.0004) after low- and high-altitude trekking, whereas ˙ QaO2 kinetics and Cw did not change. Percentages of slow and fast isoforms of MyHC and mitochondrial mass were not affected by low- and high-altitude training. After training altitude, muscle fiber ADP-stimulated mitochondrial respiration was decreased as compared with the control condition (P = 0.016), whereas leak respiration was increased (P = 0.031), leading to a significant increase in the respiratory control ratio (P = 0.016). CONCLUSIONS: Although training did not significantly modify muscle phenotype, it induced beneficial adaptations of the oxygen transport-utilization systems witnessed by faster VO2 kinetics at exercise onset.


Subject(s)
Altitude , Muscle, Skeletal/metabolism , Oxygen Consumption/physiology , Physical Endurance/physiology , Walking , Adult , Female , Humans , Middle Aged , Myosin Heavy Chains/metabolism , Oxygen/metabolism , Quadriceps Muscle/metabolism
2.
Acta Physiol (Oxf) ; 215(1): 58-71, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25965867

ABSTRACT

AIM: To parse out the impact of advanced ageing and disuse on skeletal muscle function, we utilized both in vivo and in vitro techniques to comprehensively assess upper- and lower-limb muscle contractile properties in 8 young (YG; 25 ± 6 years) and 8 oldest-old mobile (OM; 87 ± 5 years) and 8 immobile (OI; 88 ± 4 years) women. METHODS: In vivo, maximal voluntary contraction (MVC), electrically evoked resting twitch force (RT), and physiological cross-sectional area (PCSA) of the quadriceps and elbow flexors were assessed. Muscle biopsies of the vastus lateralis and biceps brachii facilitated the in vitro assessment of single fibre-specific tension (Po). RESULTS: In vivo, compared to the young, both the OM and OI exhibited a more pronounced loss of MVC in the lower limb [OM (-60%) and OI (-75%)] than the upper limb (OM = -51%; OI = -47%). Taking into account the reduction in muscle PCSA (OM = -10%; OI = -18%), only evident in the lower limb, by calculating voluntary muscle-specific force, the lower limb of the OI (-40%) was more compromised than the OM (-13%). However, in vivo, RT in both upper and lower limbs (approx. 9.8 N m cm(-2) ) and Po (approx. 123 mN mm(-2) ), assessed in vitro, implies preserved intrinsic contractile function in all muscles of the oldest-old and were well correlated (r = 0.81). CONCLUSION: These findings suggest that in the oldest-old, neither advanced ageing nor disuse, per se, impacts intrinsic skeletal muscle function, as assessed in vitro. However, in vivo, muscle function is attenuated by age and exacerbated by disuse, implicating factors other than skeletal muscle, such as neuromuscular control, in this diminution of function.


Subject(s)
Elbow/physiology , Extremities/physiology , Muscle Contraction/physiology , Muscle Strength/physiology , Muscle, Skeletal/physiology , Adaptation, Physiological/physiology , Adult , Aged, 80 and over , Aging , Humans , Quadriceps Muscle/physiology , Young Adult
3.
Am J Physiol Cell Physiol ; 308(2): C123-38, 2015 Jan 15.
Article in English | MEDLINE | ID: mdl-25354526

ABSTRACT

Muscle-specific ankyrins 1 (sAnk1) are a group of small ankyrin 1 isoforms, of which sAnk1.5 is the most abundant. sAnk1 are localized in the sarcoplasmic reticulum (SR) membrane from where they interact with obscurin, a myofibrillar protein. This interaction appears to contribute to stabilize the SR close to the myofibrils. Here we report the structural and functional characterization of skeletal muscles from sAnk1 knockout mice (KO). Deletion of sAnk1 did not change the expression and localization of SR proteins in 4- to 6-mo-old sAnk1 KO mice. Structurally, the main modification observed in skeletal muscles of adult sAnk1 KO mice (4-6 mo of age) was the reduction of SR volume at the sarcomere A band level. With increasing age (at 12-15 mo of age) extensor digitorum longus (EDL) skeletal muscles of sAnk1 KO mice develop prematurely large tubular aggregates, whereas diaphragm undergoes significant structural damage. Parallel functional studies revealed specific changes in the contractile performance of muscles from sAnk1 KO mice and a reduced exercise tolerance in an endurance test on treadmill compared with control mice. Moreover, reduced Qγ charge and L-type Ca(2+) current, which are indexes of affected excitation-contraction coupling, were observed in diaphragm fibers from 12- to 15-mo-old mice, but not in other skeletal muscles from sAnk1 KO mice. Altogether, these findings show that the ablation of sAnk1, by altering the organization of the SR, renders skeletal muscles susceptible to undergo structural and functional alterations more evident with age, and point to an important contribution of sAnk1 to the maintenance of the longitudinal SR architecture.


Subject(s)
Aging/metabolism , Ankyrins/genetics , Ankyrins/metabolism , Muscle Fibers, Skeletal/metabolism , Protein Isoforms/metabolism , Sequence Deletion/genetics , Aging/genetics , Animals , Calcium Channels, L-Type/genetics , Calcium Channels, L-Type/metabolism , Female , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Muscle Contraction/genetics , Muscle Proteins/genetics , Muscle Proteins/metabolism , Protein Isoforms/genetics , Sarcoplasmic Reticulum/genetics , Sarcoplasmic Reticulum/metabolism
4.
Biogerontology ; 14(3): 303-23, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23686362

ABSTRACT

During ageing skeletal muscles undergo a process of structural and functional remodelling that leads to sarcopenia, a syndrome characterized by loss of muscle mass and force and a major cause of physical frailty. To determine the causes of sarcopenia and identify potential targets for interventions aimed at mitigating ageing-dependent muscle wasting, we focussed on the main signalling pathway known to control protein turnover in skeletal muscle, consisting of the insulin-like growth factor 1 (IGF1), the kinase Akt and its downstream effectors, the mammalian target of rapamycin (mTOR) and the transcription factor FoxO. Expression analyses at the transcript and protein level, carried out on well-characterized cohorts of young, old sedentary and old active individuals and on mice aged 200, 500 and 800 days, revealed only modest age-related differences in this pathway. Our findings suggest that during ageing there is no downregulation of IGF1/Akt pathway and that sarcopenia is not due to FoxO activation and upregulation of the proteolytic systems. A potentially interesting result was the increased phosphorylation of the ribosomal protein S6, indicative of increased activation of mTOR complex1 (mTORC1), in aged mice. This result may provide the rationale why rapamycin treatment and caloric restriction promote longevity, since both interventions blunt activation of mTORC1; however, this change was not statistically significant in humans. Finally, genetic perturbation of these pathways in old mice aimed at promoting muscle hypertrophy via Akt overexpression or preventing muscle loss through inactivation of the ubiquitin ligase atrogin1 were found to paradoxically cause muscle pathology and reduce lifespan, suggesting that drastic activation of the IGF1-Akt pathway may be counterproductive, and that sarcopenia is accelerated, not delayed, when protein degradation pathways are impaired.


Subject(s)
Aging/physiology , Forkhead Transcription Factors/physiology , Insulin-Like Growth Factor I/physiology , Muscle, Skeletal/physiology , Proto-Oncogene Proteins c-akt/physiology , Signal Transduction/physiology , TOR Serine-Threonine Kinases/physiology , Adolescent , Adult , Aged , Aged, 80 and over , Animals , Autophagy-Related Protein 7 , Female , Forkhead Box Protein O1 , Humans , Male , Mice , Mice, Inbred C57BL , Mice, Inbred DBA , Mice, Knockout , Mice, Transgenic , Microtubule-Associated Proteins/genetics , Microtubule-Associated Proteins/physiology , Models, Animal , Muscle Proteins/genetics , Muscle Proteins/physiology , SKP Cullin F-Box Protein Ligases/genetics , SKP Cullin F-Box Protein Ligases/physiology , Sarcopenia/physiopathology , Serpin E2/genetics , Serpin E2/physiology , Tripartite Motif Proteins , Ubiquitin-Protein Ligases/genetics , Ubiquitin-Protein Ligases/physiology , Young Adult
5.
Biodegradation ; 23(5): 705-16, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22367465

ABSTRACT

Nitrocellulose is one of the most commonly used compounds in ammunition and paint industries and its recalcitrance to degradation has a negative impact on human health and the environment. In this study the capability of Desulfovibrio desulfuricans ATCC 13541 to degrade nitrocellulose as binder in paint was assayed for the first time. Nitrocellulose-based paint degradation was followed by monitoring the variation in nitrate, nitrite and ammonium content in the culture medium using Ultraviolet-Visible spectroscopy. At the same time cell counts and ATP assay were performed to estimate bacterial density and activity in all samples. Infrared spectroscopy and colorimetric measurements of paint samples were performed to assess chemical and colour changes due to the microbial action. Microscope observations of nitrocellulose-based paint samples demonstrated the capability of the bacterium to adhere to the paint surface and change the paint adhesive characteristics. Finally, preliminary studies of nitrocellulose degradation pathway were conducted by assaying nitrate- and nitrite reductases activity in D. desulfuricans grown in presence or in absence of paint. We found that D. desulfuricans ATCC 13541 is able to transform nitrocellulose as paint binder and we hypothesised ammonification as degradation pathway. The results suggest that D. desulfuricans ATCC 13541 is a good candidate as a nitrocellulose-degrading bacterium.


Subject(s)
Collodion/metabolism , Desulfovibrio desulfuricans/metabolism , Paint , Biodegradation, Environmental , Color , Desulfovibrio desulfuricans/cytology , Desulfovibrio desulfuricans/enzymology , Humans , Microscopy, Fluorescence , Nitrate Reductase/metabolism , Nitrite Reductases/metabolism , Spectroscopy, Fourier Transform Infrared , Substrate Specificity
6.
Skin Pharmacol Physiol ; 25(3): 111-7, 2012.
Article in English | MEDLINE | ID: mdl-22327146

ABSTRACT

The influence of nutrition on skin health is a growing research area but the findings of various studies on the effect of diet on the development of acne have often been contradictory. The general opinion among researchers has oscillated between two different, opposing positions: that diet either is or is not a key factor for acne development. This review examines the evidence supporting an influence of various dietary components on the development of acne particularly focusing on the role played by carbohydrates. The physiological and biochemical effects of the ketogenic diet are examined from this perspective and mechanisms will be proposed via which this type of diet could have a role in the treatment of acne.


Subject(s)
Acne Vulgaris/diet therapy , Diet, Ketogenic , Dietary Carbohydrates/adverse effects , Acne Vulgaris/etiology , Acne Vulgaris/physiopathology , Diet, Ketogenic/adverse effects , Evidence-Based Medicine , Humans , Ketosis , Nutritional Status , Treatment Outcome
7.
Clin Ter ; 162(5): e145-53, 2011.
Article in Italian | MEDLINE | ID: mdl-22041813

ABSTRACT

Obesity is reaching epidemic proportions in Western countries and is a strong risk factor for cardiovascular disease. Despite the constant recommendations of health care organizations regarding the importance of weight control, this goal often fails. Although there is a common agreement about the concept that exercise and diet are two key factors for the control of body weight, the ideal amount and type of exercise and also the ideal diet for weight control are still under debate. A widely accepted nutritional regime is the Mediterranean diet that has evident health benefits although less attention has been paid to see if the effects are due to other lifestyle factors which may contribute to the health benefits perhaps as much as specific food choices. There are several other options available to the physician that may produce good weight loss results in the short/medium term and also for maintenance of the goal achieved. One of these strategies is the ketogenic diet or VLCKD (very low carbohydrate ketogenic diet) that has been widely studied in recent years. Most studies show that this diet has a solid physiological and biochemical basis which is able to induce effective weight loss and improvement of several parameters of cardiovascular risk. This review discusses the physiological basis of VLCKD and the main applications together with its strengths and weaknesses compared to common dietary recommendations.


Subject(s)
Diet, Carbohydrate-Restricted , Diet, Ketogenic , Diet, Reducing , Obesity/diet therapy , Adipose Tissue/metabolism , Cardiovascular Diseases/prevention & control , Diet, Carbohydrate-Restricted/adverse effects , Diet, Ketogenic/adverse effects , Diet, Mediterranean , Diet, Reducing/adverse effects , Dietary Carbohydrates/metabolism , Energy Metabolism , Humans , Hydroxymethylglutaryl CoA Reductases/metabolism , Ketone Bodies/metabolism , Obesity/epidemiology , Obesity/metabolism , Risk Factors , Weight Loss
8.
J Appl Physiol (1985) ; 111(6): 1597-605, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21868681

ABSTRACT

The study investigated the effect of prolonged hypoxia on central [i.e., cardiovascular oxygen delivery (Q(a)O(2))] and peripheral (i.e., O(2) utilization) determinants of oxidative metabolism response during exercise in humans. To this aim, seven male mountaineers were examined before and immediately after the Himalayan Expedition Interamnia 8000-Manaslu 2008, lasting 43 days, among which, 23 days were above 5,000 m. The subjects showed a decrease in body weight (P < 0.05) and of power output during a Wingate Anaerobic test (P < 0.05) and an increase of thigh cross-sectional area (P < 0.05). Absolute maximal O(2) uptake (VO(2max)) did not change. The mean response time of VO(2) kinetics at the onset of step submaximal cycling exercise was reduced significantly from 53.8 s ± 10.9 to 39.8 s ± 10.9 (P < 0.05), whereas that of Q(a)O(2) was not. Analysis of single fibers dissected from vastus lateralis biopsies revealed that the expression of slow isoforms of both heavy and light myosin subunits increased, whereas that of fast isoforms decreased. Unloaded shortening velocity of fibers was decreased significantly. In summary, independent findings converge in indicating that adaptation to chronic hypoxia brings about a fast-to-slow transition of muscle fibers, resulting in a faster activation of the mitochondrial oxidative metabolism. These results indicate that a prolonged and active sojourn in hypoxia may induce muscular ultrastructural and functional changes similar to those observed after aerobic training.


Subject(s)
Altitude , Exercise/physiology , Mountaineering/physiology , Muscle Fibers, Skeletal/physiology , Oxygen Consumption/physiology , Acclimatization/physiology , Adult , Biomechanical Phenomena , Humans , Hypoxia/physiopathology , Kinetics , Male , Middle Aged , Mitochondria, Muscle/physiology , Muscle Fibers, Skeletal/classification , Myosins/physiology
9.
Anal Bioanal Chem ; 401(6): 1827-37, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21725834

ABSTRACT

Natural organic materials used to prepare pharmaceutical mixtures including ointments and balsams have been characterized by a combined non-destructive spectroscopic analytical approach. Three classes of materials which include vegetable oils (olive, almond and palm tree), gums (Arabic and Tragacanth) and beeswax are considered in this study according to their widespread use reported in ancient recipes. Micro-FTIR, micro-Raman and fluorescence spectroscopies have been applied to fresh and mildly thermally aged samples. Vibrational characterization of these organic compounds is reported together with tabulated frequencies, highlighting all spectral features and changes in spectra which occur following artificial aging. Synchronous fluorescence spectroscopy has been shown to be particularly useful for the assessment of changes in oils after aging; spectral difference between Tragacanth and Arabic gum could be due to variations in origin and processing of raw materials. Analysis of these materials using non-destructive spectroscopic techniques provided important analytical information which could be used to guide further study.


Subject(s)
Balsams/chemistry , Ointments/chemistry , Spectrometry, Fluorescence/methods , Spectroscopy, Fourier Transform Infrared/methods , Spectrum Analysis, Raman/methods , Technology, Pharmaceutical/history , Gum Arabic/analysis , History, Ancient , Plant Oils/analysis , Waxes/analysis
10.
Anal Bioanal Chem ; 401(6): 1847-60, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21667062

ABSTRACT

Chemical analysis of ancient residues of pharmaceutical or cosmetic preparations such as balms or ointments is made problematic by the high complexity of these mixtures, composed of organic and inorganic materials. Consequently, a multi-analytical approach and special caution in the interpretation of the results are necessary. In order to contribute to the improvement of analytical strategies for the characterization of complex residues and to reconstruct ancient medical practices, a replica of a pharmaceutical formulation of the seventeenth century was prepared in the laboratory according to a historically documented recipe. In a round robin exercise, a portion of the preparation was analysed as a blind sample by 11 laboratories using various analytical techniques. These included spectroscopic, chromatographic and mass spectrometric methods. None of the laboratories was able to completely reconstruct the complex formulation, but each of them gave partial positive results. The round robin exercise has demonstrated that the application of a multi-analytical approach can permit a complete and reliable reconstruction of the composition. Finally, on the basis of the results, an analytical protocol for the study of residues of ancient medical and pharmaceutical preparations has been outlined.


Subject(s)
Ointments/chemistry , Technology, Pharmaceutical/history , Chromatography, High Pressure Liquid , Gas Chromatography-Mass Spectrometry , History, 17th Century , Magnetic Resonance Spectroscopy , Mass Spectrometry , Spectroscopy, Fourier Transform Infrared , Spectrum Analysis, Raman
11.
J Biol Regul Homeost Agents ; 25(4): 635-45, 2011.
Article in English | MEDLINE | ID: mdl-22217995

ABSTRACT

The effects of a hypobaric, hypoxic environment and exercise performed under extreme conditions, such as at high altitudes, are intriguing physiological aspects that need to be investigated directly on human climbers. Their skeletal muscle is one of the main tissues that can suffer from hypoxia and physical challenges, which will both define the muscle adaptation and the molecular signature of regenerative capacity. We investigated the muscle regenerative capacity characterizing satellite cells. Our study shows that satellite cells are altered by hypobaric, hypoxic environments and exercise performed at high altitudes. Of note, in human skeletal muscle after this 5,000 m a.s.l. expedition, SCs showed a significantly lower ability to regenerate skeletal muscle, in respect to before this high-altitude expedition. This impairment appears to be due to reduced satellite cell activity, consistent with their decreased myogenicity and fusion ability. Furthermore, at the transcriptional level several pathways, such as cell cycle, myogenesis, oxidative metabolism, proteolysis and sarcomeric protein synthesis, were found dysregulated.


Subject(s)
Hypoxia/pathology , Muscle, Skeletal/pathology , Adaptation, Physiological , Adult , Altitude , Exercise , Humans , Hypoxia/physiopathology , Male , Middle Aged , Muscle, Skeletal/physiology , Proteolysis , Regeneration , Satellite Cells, Skeletal Muscle/physiology
12.
Int J Immunopathol Pharmacol ; 22(3): 795-807, 2009.
Article in English | MEDLINE | ID: mdl-19822097

ABSTRACT

Chronic fatigue syndrome (CFS) is a disabling condition characterized by unexplained chronic fatigue that impairs normal activities. Many body systems are affected and etiology has not yet been identified. In addition to immunological and psychological aspects, skeletal muscle symptoms are prominent in CFS patients. In an effort to establish which pathways might be involved in the onset and development of muscle symptoms, we used global transcriptome analysis to identify genes that were differentially expressed in the vastus lateralis muscle of female and male CFS patients. We found that the expression of genes that play key roles in mitochondrial function and oxidative balance, including superoxide dismutase 2, were altered, as were genes involved in energy production, muscular trophism and fiber phenotype determination. Importantly, the expression of a gene encoding a component of the nicotinic cholinergic receptor binding site was reduced, suggesting impaired neuromuscular transmission. We argue that these major biological processes could be involved in and/or responsible for the muscle symptoms of CFS.


Subject(s)
Fatigue Syndrome, Chronic/genetics , Gene Expression Profiling , Quadriceps Muscle/chemistry , Adult , Atrophy/genetics , Biopsy , Case-Control Studies , DNA Repair/genetics , Energy Metabolism/genetics , Fatigue Syndrome, Chronic/metabolism , Fatigue Syndrome, Chronic/pathology , Female , Gene Expression Profiling/methods , Gene Expression Regulation , Genotype , Humans , Male , Middle Aged , Neuromuscular Junction/genetics , Oligonucleotide Array Sequence Analysis , Oxidative Stress/genetics , Phenotype , Quadriceps Muscle/pathology
14.
Int J Immunopathol Pharmacol ; 22(2): 427-36, 2009.
Article in English | MEDLINE | ID: mdl-19505395

ABSTRACT

Chronic fatigue syndrome (CFS) is a disabling condition characterized by unexplained chronic fatigue that impairs normal activities. Although immunological and psychological aspects are present, symptoms related to skeletal muscles, such as muscle soreness, fatigability and increased lactate accumulation, are prominent in CFS patients. In this case-control study, the phenotype of the same biopsy samples was analyzed by determining i) fibre-type proportion using myosin isoforms as fibre type molecular marker and gel electrophoresis as a tool to separate and quantify myosin isoforms, and ii) contractile properties of manually dissected, chemically made permeable and calcium-activated single muscle fibres. The results showed that fibre-type proportion was significantly altered in CSF samples, which showed a shift from the slow- to the fast-twitch phenotype. Cross sectional area, force, maximum shortening velocity and calcium sensitivity were not significantly changed in single muscle fibres from CSF samples. Thus, the contractile properties of muscle fibres were preserved but their proportion was changed, with an increase in the more fatigue-prone, energetically expensive fast fibre type. Taken together, these results support the view that muscle tissue is directly involved in the pathogenesis of CSF and it might contribute to the early onset of fatigue typical of the skeletal muscles of CFS patients.


Subject(s)
Calcium Signaling , Fatigue Syndrome, Chronic/metabolism , Muscle Contraction , Muscle Fibers, Fast-Twitch/metabolism , Muscle Fibers, Slow-Twitch/metabolism , Adult , Biopsy , Case-Control Studies , Fatigue Syndrome, Chronic/pathology , Fatigue Syndrome, Chronic/physiopathology , Female , Humans , Male , Middle Aged , Muscle Fatigue , Muscle Fibers, Fast-Twitch/pathology , Muscle Fibers, Slow-Twitch/pathology , Myosins/metabolism , Phenotype , Protein Isoforms
15.
J Biotechnol ; 127(4): 670-8, 2007 Jan 20.
Article in English | MEDLINE | ID: mdl-17007953

ABSTRACT

Polyketone polymer -[-CO-CH(2)-CH(2)-](n)-, obtained by copolymerization of ethene and carbon monoxide, is utilized for immobilization of three different enzymes, one peroxidase from horseradish (HRP) and two amine oxidases, from bovine serum (BSAO) and lentil seedlings (LSAO). The easy immobilization procedure is carried out in diluted buffer, at pH 7.0 and 3 degrees C, gently mixing the proteins with the polymer. No bifunctional reagents and spacer arms are required for the immobilization, which occurs exclusively via a large number of hydrogen bonds between the carbonyl groups of the polymer and the -NH groups of the polypeptidic chain. Experiments demonstrate a high linking capacity of polymer for BSAO and an extraordinary strong linkage for LSAO. Moreover, activity measurements demonstrate that immobilized LSAO totally retains the catalytic characteristics of the free enzyme, where only a limited increase of K(M) value is observed. Finally, the HRP-activated polymer is successfully used as active packed bed of an enzymatic reactor for continuous flow conversion and flow injection analysis of hydrogen peroxide containing solutions.


Subject(s)
Enzymes, Immobilized/chemistry , Ketones/chemistry , Polymers/chemistry , Biotechnology , Carbon Monoxide/chemistry , Ethylenes/chemistry , Hydrogen Bonding , Hydrogen-Ion Concentration , Molecular Structure , Peroxidase/chemistry
16.
J Exp Biol ; 208(Pt 22): 4243-53, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16272247

ABSTRACT

This study aimed to analyse the expression of myosin heavy chain (MHC) isoforms in bovine muscles, with particular attention to the MHC-2B gene. Diaphragm, longissimus dorsi, masseter, several laryngeal muscles and two extraocular muscles (rectus lateralis and retractor bulbi) were sampled in adult male Bos taurus (age 18-24 months, mass 400-500 kg) and analysed by RT-PCR, gel electrophoresis and immunohistochemistry. Transcripts and proteins corresponding to eight MHC isoforms were identified: MHC-alpha and MHC-beta/slow (or MHC-1), two developmental isoforms (MHC-embryonic and MHC-neonatal), three adult fast isoforms (MHC-2A, MHC-2X and MHC-2B) and the extraocular isoform MHC-Eo. All eight MHC isoforms were found to be co-expressed in extrinsic eye muscles, retractor bulbi and rectus lateralis, four (beta/slow, 2A, 2X, neonatal) in laryngeal muscles, three (beta/slow, 2A and 2X) in trunk and limb muscles and two (beta/slow and alpha) in masseter. The expression of MHC-2B and MHC-Eo was restricted to extraocular muscles. Developmental MHC isoforms (neonatal and embryonic) were only found in specialized muscles in the larynx and in the eye. MHC-alpha was only found in extraocular and masseter muscle. Single fibres dissected from masseter, diaphragm and longissimus were classified into five groups (expressing, respectively, beta/slow, alpha, slow and 2A, 2A and 2X) on the basis of MHC isoform electrophoretical separation, and their contractile properties [maximum shortening velocity (v(0)) and isometric tension (P(0))] were determined. v(0) increased progressively from slow to fast 2A and fast 2X, whereas hybrid 1-2A fibres and fibres containing MHC-alpha were intermediate between slow and fast 2A.


Subject(s)
Cattle/metabolism , Muscle, Skeletal/metabolism , Myosin Heavy Chains/metabolism , Analysis of Variance , Animals , DNA Primers , Electrophoresis, Polyacrylamide Gel , Gene Expression Profiling , Immunohistochemistry , Male , Protein Isoforms/metabolism , Reverse Transcriptase Polymerase Chain Reaction
18.
Talanta ; 63(4): 967-77, 2004 Jul 08.
Article in English | MEDLINE | ID: mdl-18969524

ABSTRACT

This paper describes an analytical approach to investigate the origin of oxalate films on marble. Calcium oxalate films were collected on buildings of historical importance in Lucca and Pisa (Italy) and characterised by optical microscopy (OM), scanning electron microscopy-energy dispersive X-ray spectrometry (SEM-EDX), Fourier transform infrared (FTIR) spectroscopy (equipped with diamond cell), and gas chromatography-mass spectrometry (GC-MS). The morphology of the films was investigated by optical and electronic microscopy. FTIR analyses highlighted the presence of calcium oxalate (both as whewellite and weddellite), gypsum, calcite, nitrates, silicates and apatite, while EDX maps showed the distribution of elements. Several samples showed traces of organic compounds, identified by GC-MS as paraffin wax, lipids of animal origin and egg. The correlation between organic material and oxalate contents suggests the origin of the films from degradation processes of past surface treatment.

19.
Eur J Histochem ; 48(4): 357-66, 2004.
Article in English | MEDLINE | ID: mdl-15718201

ABSTRACT

Myosin heavy chain isoforms (MHC) of adult skeletal muscles are codified by four genes named: slow, or type 1, and fast types 2A, 2X and 2B. The slow, 2A and 2X isoforms have been found expressed in all mammalian species studied so far whereas there is a large inter-species variability in the expression of MHC-2B. In this study histochemistry (m-ATPase), immunohistochemistry with the use of specific monoclonal antibodies and RT-PCR were combined together to assess whether the MHC-2B gene is expressed in bovine muscles. ATPase staining and RT-PCR experiments showed that three MHC isoforms (1, 2A, 2X) were expressed in trunk and limb muscles. Slow or type 1 expression was confirmed using a specific antibody (BA-F8) whereas the detection of fast MHC isoforms were validate by means of BF-35 antibody although not by the SC-71 antibody. MHC-2B was absent in limb and trunk muscles, but was present in specialized eye muscles (rectus lateralis and retractor bulbi) as consistently showed by RT-PCR and reactivity with a specific antibody (BF-F3). Interestingly, a cardiac isoform, MHC-a-cardiac was found to be expressed not only in extraocular muscles but also in masticatory muscles as masseter.


Subject(s)
Cattle/metabolism , Myosin Heavy Chains/metabolism , Oculomotor Muscles/metabolism , Skeletal Muscle Myosins/metabolism , Animals , Base Sequence , Cattle/genetics , Histocytochemistry , Immunochemistry , Molecular Sequence Data , Myosin Heavy Chains/genetics , Phylogeny , Reverse Transcriptase Polymerase Chain Reaction , Skeletal Muscle Myosins/genetics
20.
Ann Chim ; 91(11-12): 741-8, 2001.
Article in English | MEDLINE | ID: mdl-11836951

ABSTRACT

Some new protective copolymers and a commercial one have been tested on Candoglia marble, a very low porosity stone. Two of the polymers contained a partially fluorinated methacrylic monomer, 2,2,2 trifluoro ethyl methacrylate (TFEMA), in combination with either an acrylic, methyl acrylate (MA) or a vinyl ether, n-butyl vinyl ether (n-BVE) unit. Two copolymers, ethyl methacrylate/n-butyl vinyl ether and ethyl methacrylate (EMA)/methyl acrylate (Paraloid B72), were non-fluorinated and similar in compositions and molar ratio. The aim of the work is to test the copolymers and compare the performances of fluorinated new polymers with the non fluorinated one and with the largely used commercial product. The results obtained demonstrate that the introduction, even in limited amounts, of fluorine atoms in the side ester groups of methacrylic type polymers really improves their protective effect and the durability of the stone treatments. The best results were obtained with the copolymer TFEM/MA which is the fluorinated homologous of Paraloid B72.


Subject(s)
Acrylates/chemistry , Calcium Carbonate/chemistry , Fluorocarbon Polymers/chemistry , Polymers/chemistry , Colorimetry , Microscopy, Electron, Scanning , Oxidation-Reduction , Photochemistry , Surface Properties
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