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PubMed2007

Isolation and chondroinduction of a dermis-isolated, aggrecan-sensitive subpopulation with high chondrogenic potential.

OBJECTIVE: To develop a process that yields tissue-engineered articular cartilage constructs from skin-derived cells. METHODS: Dermis-isolated, aggrecan-sensitive (DIAS) cells were isolated using a modified rapid adherence process. The chondrogenic potential was measured by quantitative reverse transcriptase-polymerase chain reaction, enzyme-linked immunosorbent assay, and immunohistochemistry. Filamentous actin (F-actin) and vinculin organization was detected using fluorescence microscopy. RESULTS: The rapid adherence process led to a selection of DIAS cells, <10% of the entire population. DIAS cells displayed greater chondroinduction potential, as evidenced by the formation of large numbers of chondrocytic nodules on aggrecan-coated surfaces. In addition, these cells showed higher gene expression and protein production in terms of chondrocytic markers when compared with unpurified dermis cells. Similar patterns of F-actin and vinculin organization were observed between DIAS cells and chondrocytes. Three-dimensional constructs from chondroinduced DIAS cells produced greater amounts of cartilage matrix than constructs from the rest of the dermis populations. CONCLUSION: These findings show a series of steps that work together to form tissue-engineered articular cartilage constructs using DIAS cells. Since skin presents a minimally invasive, relatively abundant cell source for tissue engineering, this study offers evidence of an efficient and stable technique to form cartilage constructs for future cartilage regeneration with autologous cells from skin.

Actin Cytoskeleton↗
PubMed1993

Postnatal expression of myosin isoforms in the genioglossus and diaphragm muscles.

We studied the expression of myosin heavy chain (MHC) and native myosin isoforms in the genioglossus (GG) and costal diaphragm (DIA) muscles of the rat during postnatal development using both denaturing and nondenaturing gel electrophoresis. Primary myotubes in both fast and slow muscles homogeneously express slow as well as embryonic myosin. Since the adult GG is comprised primarily of fast MHC isoforms, whereas the adult DIA is characterized by a mixture of MHC slow and fast isoforms, we hypothesized that the GG and DIA would be subject to different temporal patterns of MHC isoform expression during postnatal development. Native myosin and MHC gels demonstrated a persistence of neonatal MHC (MHC neo) on day 25 in the GG, whereas this isoform was not detected beyond day 21 in the DIA. The MHC phenotype in GG of the adult demonstrated a predominance of MHC 2X (35% +/- 8) and MHC 2B (45% +/- 10) with a smaller proportion of MHC 2A (19% +/- 5). In contrast, the MHC phenotype in adult DIA was characterized by approximately equal proportions of MHC slow (25% +/- 3), MHC 2A (34% +/- 10), and MHC 2X (31% +/- 12) with a small percentage of MHC 2B (9% +/- 7). These data suggest that postnatal regulation of MHC expression in the GG and DIA is muscle specific.

Analysis of Variance↗
PubMed1999

GM-CSF stimulates proliferation of clonal leukemic bone marrow cells in acute myeloid leukemia (AML) in vitro.

Granulocyte-macrophage colony-stimulating factor (GM-CSF) is known to stimulate granulocytes, monocytes, and macrophages. We studied the effect of GM-CSF on (clonal) bone marrow (BM) cells obtained from AML patients after 7 days of culture in vitro: BM samples were obtained from 19 AML patients at diagnosis (DIA), from two patients with persisting disease (PERS), from eight patients in complete remission (CR), and from 12 healthy donors. Flow-cytometric comparison of differentiated, CD 15-positive cells or of CD34-positive blast cells before and after cultivation showed that the proportion of CD15-positive cells was increased in nine of 12 healthy BM samples, in 14 of 19 cases at DIA, in one of three cases during PERS, and in five of six cases in CR of AML. The proportion of CD34-positive cells was increased in one of 12 healthy BM samples, in seven of 19 cases at DIA, in one of two cases during PERS, and in three of seven cases in CR of AML. Southern blot analysis (SBA) performed in six cases during the course of AML, before and after cell culture, showed that clonal DNA increased after GM-CSF treatment in three of five cases studied at DIA, in six of nine cases studied in CR, in the one case studied at PERS, and in the one studied at relapse (REL). In one case of trisomy 8 at DIA a normal karyotype was demonstrated in CR. However, after 7 days of cultivation of the cells in GM-CSF the trisomy 8 was detected in two of 17 metaphases isolated from colony-cells from methylcellulose cultures. Our data show that a 7-day treatment of BM cells with GM-CSF induced a differentiation of healthy and leukemic BM cells in the great majority of cases. An enrichment of CD34-positive cells was not achieved in healthy BM samples. However, in 70% of the cases in CR and in 30% of the cases at DIA of AML, clonal CD34-positive cells were enriched. This means that GM-CSF stimulates ('primes') leukemic cell growth in vitro.

Antigens, CD34↗
PubMed1987

Isoenzyme studies in human leukemia-lymphoma cell lines--V. Induction of differentiation by T-cell derived differentiation-inducing activity.

A panel of human leukemia cell lines from various lineages (T-cell, pre B- and Non-T/Non-B cell, myelomonocytic and erythroleukemia cell lines) were utilised as model systems of the distant effects of differentiation-inducing activity (DIA) produced by the T-leukemia cell line HUT-102. DIA inhibited cell proliferation and induced distinct morphological changes which were more pronounced in the myelomonocytic and erythroleukemia cell lines than in the lymphoid cell lines. DIA triggered in the myelomonocytic and erythroleukemia cell lines an increase in the number of NBT-reducing cells and caused strong adherence to plastic surface. The T-cell lines showed aggregation of cells in floating clusters. In the isoenzyme analysis of the enzymes carboxylic esterase and acid phosphatase, it was found that DIA stimulated the new expression of isoenzymes and a stronger staining intensity of several isoenzyme bands in all cell lines, however, at varying degrees. HL-60 and HEL displayed newly a monocyte-specific isoenzyme. Several myelomonocytic and erythroleukemia cell lines were triggered to express the tartrate-resistant acid phosphatase isoenzyme. The cell kinetic, morphological, functional and isoenzymatic data demonstrated that DIA effected the development of the different blood cell types. However, it appears that the cells reached a new differentiation block after acquired expression of differentiation-linked features; the lymphoid cell lines were more limited in their response to DIA than the myeloid and erythroid cells.

Acid Phosphatase↗
PubMed2006

Influence of diaphragm and rib cage muscle fatigue on breathing during endurance exercise.

Inspiratory muscle fatigue (IMF) can develop during exhaustive exercise and cause tachypnea or rapid shallow breathing. We assessed the effects of rib cage muscle (RCM-F) and diaphragm fatigue (DIA-F) on breathing pattern and respiratory mechanics during high-intensity endurance exercise. Twelve healthy subjects performed a constant-load (85% maximal power) cycling test to exhaustion with prior IMF and a cycling test of similar intensity and duration without prior IMF (control). IMF was induced by resistive breathing and assessed by oesophageal and gastric twitch pressure measurements during cervical magnetic stimulation. Both RCM-F and DIA-F increased RCM and abdominal muscle force production during exercise compared to control. With RCM-F, tidal volume decreased while it increased with DIA-F. RCM-F was associated with a smaller increase in end-expiratory oesophageal pressure (i.e. decrease in lung volume) than DIA-F. These results suggest that RCM-F and not DIA-F is associated with rapid shallow breathing and that lowering the operating lung volume with DIA-F may help to preserve diaphragmatic function.

Adult↗
PubMed2000

The effect of stimulus form and dimensions on the oral size illusion in humans.

Previous work has shown that individuals overestimate the diameter of holes presented to the tongue when they use their fingers to select matching holes from a range of comparators. This disparity is known as the oral size illusion. The hypothesis that this illusion arises from the greater pliability of the tongue surface compared with that of the fingertip was tested here. Two experiments were carried out on 64 participants. In experiment 1 (n=32), the stimuli were two sets of holes, 1 and 5 mm deep and 2.4, 5.6, 8.2, 12 mm dia. , which were presented to the tongue. The comparator was a series of holes 5 mm deep and 0.8-15 mm dia., which were explored manually. Participants significantly overestimated all diameters of the 1- and 5-mm deep stimulus holes (p<0.05). Apart from the 2.4-mm dia. holes, there were no significant differences between the illusions produced with the holes 1 mm and 5 mm deep (p0.7). In experiment 2 (n=32) individuals were tested with small cylinders ('pegs') 1 mm high and 2.6, 5.2. 7.6, 12.6 mm dia. and also with the four 5-mm deep stimulus holes used in experiment 1. The 'peg' stimuli presented to the tongue were matched against a similar set of 1-mm pegs, 2-18 mm dia., explored with the fingers. The comparator series for the 5-mm deep holes was the same as for experiment 1. Participants consistently overestimated the size of the 5-mm holes (p<0.001). However, there was no illusion with the peg stimuli (p=0.08), except for the 7.6-mm dia. stimulus (p<0.05). The results of experiment 1 did not support the experimental hypothesis that the oral size illusion was due to the greater pliability of the tongue surface. The result of experiment 2 suggests that the oral size illusion does not occur when peg stimuli are used instead of holes. The form and diameter of the stimulus is thus important in determining the magnitude of the oral size illusion.

Adolescent↗
PubMed2001

An object-oriented framework for dynamic ecosystem modeling: application for integrated risk assessment.

Ecological risk assessment requires the integration of a wide range of data on anthropogenic processes, ecological processes and on processes related to environmental fate and transport. It is a major challenge to assemble a simulation system that can successfully capture the dynamics of complex ecological systems and an even more serious challenge to be able to adapt such a simulation to shifting and expanding analytical requirements and contexts. The dynamic information architecture system (DIAS) is a flexible, extensible, object-based framework for developing and maintaining complex simulations. DIAS supports simulations in which the real-world entities that make up ecological systems are represented as software 'entity objects'. The object-oriented integrated dynamic landscape analysis and modeling system (OO-IDLAMS) provides a good example of how DIAS has been used to build a suite of models for the purpose of assessing the ecological impacts of military land use and land management practices. OO-IDLAMS is a prototype conservation modeling suite that provides military environmental managers and decision-makers with a strategic, integrated and adaptive approach to natural resources planning and ecosystem management. The OO-IDLAMS prototype used Fort Riley, Kansas as a case study to demonstrate DIAS' capabilities to offer flexibility, interprocess dynamics and cost-effective reuse of code for ecosystem modeling and simulation. DIAS can also readily lend itself to other applications in ecological risk assessment. It has great potential for the integration of ecological models (associated with biological uptake and effects) with environmental fate and transport models. A DIAS ecological risk assessment application could be used to predict the magnitude and extent of ecological risks and evaluate remedy effectiveness in a timely and cost-effective manner.

Animals↗
PubMed2005

Adsorption of atrazine, hydroxyatrazine, deethylatrazine, and deisopropylatrazine onto Fe(III) polyhydroxy cations intercalated vermiculite and montmorillonite.

This paper describes the modification of the clay minerals vermiculite (VT) and montmorillonite (MT) by intercalating Fe(III) polymers of different [OH(-)]:[Fe(III)] ratios with the aim of removing atrazine (AT) and its metabolites deethylatrazine (DEA), deisopropylatrazine (DIA), and hydroxyatrazine (ATOH) from aqueous solution. An enhancement of adsorption capacity was observed for both intercalated clay minerals in comparison to the potassium-saturated materials (KVT or KMT). The results showed that different [OH(-)]:[Fe(III)] molar ratios had a small influence on the adsorption capacity, as well as in the basal spacing, BET surface area, and porosity. For the lowest initial concentrations of AT, DIA, and ATOH (0.050 mg L(-)(1)) studied, the modified VT adsorbed almost 80% of AT and DIA, while ATOH was removed at concentration levels below the detection limit of the technique, implying in at least 99.5% of sorption. Weak interaction between intercalated VT and DEA was observed, although a significant adsorption enhancement occurred in comparison to KVT. Within a 24 h interval, desorption of AT and DIA in aqueous medium reached levels close to 20% of the amount initially adsorbed, while for ATOH only 3% of the adsorbed compound was desorbed. The adsorption capacity of the Fe(III)-intercalated VT decreased after the first adsorption/desorption cycle, implying that the material is not suitable for reutilization. The intercalated MT was a powerful sorbent for AT, DEA, DIA, and ATOH, removing all of these chemicals from solution almost quantitatively (sorption greater than 99.5%), even at initial concentrations as high as 1.0 mg L(-)(1). Additionally, desorption of AT, ATOH, and DIA in water was not measurable up to the tube corresponding to the initial concentration of 1.0 mg L(-)(1), suggesting strong irreversible binding of these compounds to the intercalated MT materials. Desorption of DEA from the intercalated MT was between 5 and 30%. Unlike what was observed for VT, the intercalated MT materials were recyclable, keeping an excellent performance when reutilized.

Adsorption↗
PubMed1997

Amenorrhea induced by adjuvant chemotherapy in early breast cancer patients: prognostic role and clinical implications.

BACKGROUND: The role of amenorrhea induced by chemotherapy in premenopausal women with early breast cancer is very controversial. Analyses by various authors of the effect of drug-induced amenorrhea (DIA) on treatment outcome have yielded conflicting results. In order to gain insight into the role of DIA, we reviewed all published data addressing the issue of DIA as a prognostic factor. METHODS: Computerised and manual searches were conducted of relevant studies published from 1966 to 1995. RESULTS: Thirteen studies involving 3929 patients were selected. In two papers, the prognostic role of DIA was analysed in three and two different groups of patients, respectively. Overall, 16 groups of patients were evaluated. With 12 groups, a higher disease free survival was observed in patients developing DIA compared to those who did not. This difference was statistically significant in eight groups. Data on overall survival, reported in only five studies, indicated that it was always improved in patients who became amenorrheic. CONCLUSIONS: Available data on the role of DIA support its importance as a favorable prognostic factor for early breast cancer patients. However, due to the possible biases of this type of evaluation, this result should be interpreted with caution.

Amenorrhea↗
PubMed2000

A preliminary comparative study of a dipstick colloidal dye immunoassay and two antigen-detection ELISAs for diagnosis of Trypanosoma evansi infection in cattle.

A dipstick colloidal dye immunoassay (DIA) was developed for the field diagnosis of Trypanosoma evansi infection using affinity-purified polyclonal antibodies (PcAbs) and the monoclonal antibody (McAb) 8B9. PcAbs were adsorbed onto Palanil Red dye particles and used as dye reagents. Dipsticks were dotted with four different antibodies; normal rabbit and mouse IgGs as negative controls, and anti-T. evansi PcAb and McAb 8B9, which capture trypanosome antigens in the tested samples. Since the dye reagent bound to the captured antigens, the presence of coloured dots on the dipstick identified trypanosome infections. The sensitivity of the DIA was compared with two antigen detection ELISAs (Ag-ELISA); one was PcAb-based and the other was based on a combination of the same Mc- and PcAbs as were employed for the DIA. With a positive serum, the DIA detected trypanosomal antigen up to a dilution of 1:500 for both the PcAb and McAb dots, at which dilution the PcAb- and combination-based Ag-ELISA gave positive OD readings of 0.13 and 0.36, respectively. When 124 field sera were tested, circulating antigens were detected in 51 (41%) samples by the DIA, and 76 (61%) and 49 (40%) samples by the PcAb- and combination-based Ag-ELISAs respectively, of which 48 (63%) and 34 (69%) were also positive by the DIA.

Animals↗
PubMed1981

Dynamic properties of the inferior rectus, extensor digitorum longus, diaphragm and soleus muscles of the mouse.

1. Isometric responses to direct stimulation of inferior rectus (IR), extensor digitorum longus (EDL) and soleus (SOL) muscles and strips of diaphragm (DIA) muscle of the mouse were obtained. 2. The IR, EDL and DIA were qualitatively 'fast-twitch', while the SOL was 'slow-twitch'. The isometric twitch contraction time was for IR, 3.7 ms; EDL, 6.9 ms; DIA, 13.2 ms; SOL, 20.9 ms (at 35 degrees C). Twitch: tetanus ratio for IR was unusually small (0.12) whereas that of DIA was unusually large (0.31). 3. The force-velocity properties of the muscles were determined and the sarcomere speed of shortening calculated. The intrinsic speeds of shortening of EDL and IR were not significantly different from each other, and were 49.5 and 51.6 micrometers . s-1 respectively; the value for SOL was 23.1 micrometers . s-1 and the DIA was intermediate at 39.7 micrometers . s-1. 4. The time course of the isometric twitch of the IR was about half that of the EDL whereas the force-velocity properties of these two muscles were almost identical. This is very similar to the situation in the rat. 5. Some of the dynamic properties of the DIA were clearly intermediate between the typical 'fast-twitch' EDL and IR and the typical 'slow-twitch' SOL. This does not agree with the available histochemical evidence which suggests that the mouse diaphragm is a 'fast-twitch red' muscle.

Animals↗
PubMed1990

Comparison of a dot immunobinding assay, latex agglutination, and cytotoxin assay for laboratory diagnosis of Clostridium difficile-associated diarrhea.

C. diff-CUBE, a dot immunobinding assay (DIA) (Difco Laboratories, Ann Arbor, Mich.) for detection of Clostridium difficile toxin A in stool specimens, was compared with latex agglutination (LA) (Marion Laboratories, Kansas City, Mo.) and cytotoxin assay (CTA) for the laboratory diagnosis of C. difficile-associated diarrhea. A total of 200 stool specimens collected from 169 patients with suspected C. difficile diarrhea were tested. Of the 198 specimens evaluated by all three methods, 36 (18%) from 36 patients were positive by one or more of the tests. Twenty-five, 26, and 23 specimens were positive by CTA, DIA, and LA, respectively; 14 were positive by all three methods. Eight specimens yielded nonspecific LA test results; all eight were negative by CTA, and one was positive by DIA. DIA results agreed with CTA results in 183 (92%) cases and with LA results in 175 (88%) cases. CTA and LA results agreed in 179 (90%) cases. Freezing of the specimen did not appear to adversely affect either the DIA or LA test. These preliminary results suggest that C. diff-CUBE may be useful as a rapid screen for the diagnosis of C. difficile-associated diarrhea. However, for optimum laboratory diagnosis, further testing of all stools that are negative by DIA is warranted.

Bacterial Toxins↗
PubMed2001

Measurement of cytokine and adhesion molecule expression in synovial tissue by digital image analysis.

OBJECTIVE: Digital image analysis (DIA) offers the opportunity to quantify the stained area and staining intensity when synovial tissue (ST) is investigated by immunohistochemical analysis. This study aimed at determining the sensitivity of DIA compared with semiquantitative analysis (SQA). METHODS: Paired ST samples were obtained from the knee joint of 10 patients with rheumatoid arthritis (RA) with active disease and after follow up when complete clinical remission was achieved. ST samples of 10 subjects with non-inflammatory knee pain served as controls. Immunohistochemistry with antibodies against interleukin 1beta (IL1beta) and vascular cell adhesion molecule 1 (VCAM-1) was applied using two staining protocols with 3-amino-9-ethylcarbazole (AEC) or p-diethylaminobenzaldehyde (DAB) as dye. All sections were analysed semiquantitatively (0-4) and DIA of up to a maximum of 60 high power fields (HPF). The average integrated optical density was calculated as the product of the stained area (corrected for total tissue area) and the optical density. RESULTS: Both SQA and DIA enabled the assessment of differences in IL1beta and VCAM-1 expression between ST from active RA, RA in remission, and controls. SQA and DIA showed excellent correlations (IL1beta rs=0.867; p<0.0001: VCAM-1 rs=0.828; p<0.0001). A limited analysis of one region with six HPF still allowed adequate discrimination compared with an extended analysis of three regions with a total of 60 HPF. In general, the red dye (AEC) resulted in better discrimination than the brown (DAB) staining. CONCLUSION: DIA offers a reliable, reproducible, and sensitive analysis of ST sections stained for cytokines and adhesion molecules.

Adult↗
PubMed2006

SERCA overexpression reduces hydroxyl radical injury in murine myocardium.

Hydroxyl radicals (*OH) are involved in the pathogenesis of ischemia-reperfusion injury and are observed in clinical situations, including acute heart failure, stroke, and myocardial infarction. Acute transient exposure to *OH causes an intracellular Ca(2+) overload and leads to impaired contractility. We investigated whether upregulation of sarcoplasmic reticulum Ca(2+)-ATPase function (SERCA) can attenuate *OH-induced dysfunction. Small, contracting right ventricular papillary muscles from wild-type (WT) SERCA1a-overexpressing (transgenic, TG) and SERCA2a heterogeneous knockout (HET) mice were directly exposed to *OH. This brief 2-min exposure led to a transient elevation of diastolic force (F(dia)) and depression of developed force (F(dev)). In WT mice, F(dia) increased to 485 +/- 49% and F(dev) decreased to 11 +/- 3%. In sharp contrast, in TG mice F(dia) increased only to 241 +/- 17%, whereas F(dev) decreased only to 51 +/- 5% (P < 0.05 vs. WT). In HET mice, F(dia) rose more than WT (to 597 +/- 20%, P < 0.05), whereas F(dev) was reduced in a similar amount. After approximately 45 min after *OH exposure, a new steady state was reached: F(dev) returned to 37 +/- 6% and 32 +/- 6%, whereas F(dia) came back to 238 +/- 28% and 292 +/- 17% in WT and HET mice, respectively. In contrast, the sustained dysfunction was significantly less in TG mice: F(dia) and F(dev) returned to 144 +/- 20% and 67 +/- 6%, respectively. Before exposure to *OH, there is decrease in phospholamban (PLB) phosphorylation at Ser16 (pPLBSer16) and PLB phosphorylation at Thr17 (pPLBThr17) in TG mice and an increase in pPLBSer16 and pPLBThr17 in HET mice versus WT. After exposure to *OH there is decrease in pPLBSer16 in WT, TG, and HET mice but no significant change in the level of pPLBThr17 in any group. The results indicate that SERCA overexpression can reduce the *OH-induced contractile dysfunction in murine myocardium, whereas a reduced SR Ca(2+)-ATPase activity aggravates this injury. Loss of pPLB levels at Ser16 likely amplifies the differences observed in injury response.

Animals↗
PubMed1983

Effect of sleep state and hypercapnia on alae nasi and diaphragm EMGs in preterm infants.

A coordinated activation of upper airway and chest wall muscles may be crucial in maintaining airway patency and ventilation. The alae nasi (AN) and diaphragm (DIA) electromyograms (EMG) were recorded with surface electrodes in 17 unsedated healthy preterm infants during both active (AS) and quiet sleep (QS). Airflow was measured via a nasal mask pneumotachograph and integrated to obtain tidal volume. Studies were performed during inhalation of room air and mixtures of 2 and 4% CO2 in air. In room air, phasic AN EMG accompanied 45 +/- 7% of breaths during AS compared with 14 +/- 5% of breaths during QS (P less than 0.001); however, with inhalation of 4% CO2 the incidence of AN EMG increased to comparable levels in both sleep states. During room air breathing onset of AN EMG preceded that of the DIA EMG and inspiratory airflow by 41 +/- 8 ms (P less than 0.01) and 114 +/- 29 ms (P less than 0.05), respectively. Peak AN activity preceded peak DIA activity by 191 +/- 36 ms (P less than 0.01). Alteration in sleep state or increasing chemical drive did not significantly alter these temporal relationships. Nevertheless, with each increase in end-tidal CO2, peak DIA EMG and tidal volume increased while peak AN EMG only showed a consistent increase during 4% CO2 inhalation. We conclude that although there exists a mechanism that temporally coordinates AN and DIA activation, the amount of AN EMG activity with each breath is not clearly correlated with DIA activation, which may contribute to the high incidence of respiratory dysrhythmias in preterm neonates.

Diaphragm↗
PubMed1988

Somatotopy in the segmental innervation of the cat diaphragm.

A somatotopic organization in the segmental innervation of the cat diaphragm (DIA) was determined using evoked electromyographic responses and glycogen depletion of stimulated type II muscle fibers. With the use of the glycogen depletion method, the specific location and proportion of muscle fibers innervated by the fifth (C5) or sixth (C6) cervical ventral roots were determined for different regions of the DIA. The sternal and ventral portions of the costal and crural DIA regions were innervated primarily by C5. The dorsal portions of both the costal and crural regions were innervated primarily by C6. Thus the somatotopic organization in the segmental innervation of the DIA was not correlated with the anatomic division of the sternal, costal, and crural regions. Instead, the somatotopic projections of cervical ventral roots were organized in the ventrodorsal axis of each DIA region. This topographical pattern resulted in an extensive overlap of the DIA territories innervated by C5 and C6. Within a region, the fibers innervated by a specific ventral root were not randomly distributed but often followed fascicle divisions. This frequently resulted in a wide range in the proportion of fibers innervated by a ventral root even within a specific region.

Animals↗
PubMed1992

Postnatal expression of myosin isoforms in an expiratory muscle--external abdominal oblique.

We studied the postnatal expression of heavy-chain (MHC) and native myosin isoforms in an expiratory abdominal muscle of the rat, the external abdominal oblique (EO). Moreover, we contrasted EO myosin expression with that of the costal diaphragm (DIA) to draw inspiratory vs. expiratory muscle comparisons during development. Examination of MHC gels demonstrated a mature phenotype of slow and adult fast myosin isoforms at an earlier age in the EO (day 60) than in the DIA [day > 115 (adult)]. The mature MHC phenotype of the EO was characterized by a preponderance of MHC 2B, whereas the DIA was characterized by approximately equal portions of MHC slow, MHC 2A, and MHC 2X. During early postnatal development, there was a delay in the expression of MHC 2A in the EO compared with the DIA. However, MHC 2B, expressed later in development in both muscles, was noted in the EO before the DIA. We conclude that 1) the EO mature myosin phenotype is characterized by a preponderance of fast myosin isoforms and 2) the EO and DIA muscles are subject to different temporal patterns of isoform expression during postnatal development.

Abdominal Muscles↗
PubMed1993

Regulation of expiratory muscles during postnatal development in anesthetized piglets.

We compared maturation of the responses of the rib cage [triangularis sterni (TS)] and abdominal [transversus abdominis (TA)] expiratory muscles with each other and with the responses of the diaphragm (DIA) during hypercarbic and hypoxic stimulation. Studies were performed in anesthetized (urethan and chloralose) piglets of two age groups (< 6 days, n = 10; 14-21 days, n = 11) before and after bilateral cervical vagotomy. Hypercarbia (7% CO2-93% O2) was associated with comparable sustained increases in the minute electromyograms (EMGs) of both TS and TA, which were closely coupled to the DIA responses in both age groups. Hypoxia (12% O2-88% N2) caused a biphasic response of the minute EMG of both expiratory muscles and DIA; these biphasic responses were less prominent at 14-21 days than at < 6 days. Vagotomy caused an increase in the amplitude of both TS and TA (38 +/- 30 and 27 +/- 21%, respectively) as well as the DIA (45 +/- 16%) but did not affect their relative responses to chemostimulation. We conclude that during postnatal development 1) the rib cage and abdominal expiratory muscle responses to chemostimulation are coupled to each other and parallel those of the DIA and 2) the presence of vagal afferents attenuates the drive to both inspiratory and expiratory motoneurons under the current experimental conditions but does not influence the relative responses of expiratory muscles and DIA to hypercarbia or hypoxia. We speculate that comparable activation of inspiratory and expiratory pumping muscles serves to stabilize respiratory control in the face of altered chemosensory or vagal inputs during early postnatal life.

Afferent Pathways↗