Occupational biomechanics of the neck: a review and recommendations.

Musculoskeletal disorders of the neck are becoming a major concern in industry. Several studies reported the association of neck pain, discomfort, and symptoms with different occupations in industry. Thus, the main objective of this study is to review and evaluate biomechanical techniques used in analyzing the occupational factors leading to neck pain and disorders. Recommendations for future research are also discussed.     

Effects of protein synthesis inhibition during plant mitosis

The role of protein synthesis in onion root tips during mitosis has been studied, by using synchronous cell populations. Incubation in cycloheximide (CHM) or anisomycin during early or middle prophase induces the return of these cells to interphase. Therefore, it is suggested that essential proteins are synthesized, which determine the continuation of the cells in mitosis. In late prophase these treatments caused a certain delay in the entry into further stages, suggesting that a protein synthesis probably occurs which determines the duration of the transition from metaphase to anaphase. Mitotic processes which develop after metaphase do not seem morphologically dependent on protein synthesis, in spite of the fact that one of them, the nucleolar reconstruction, is markedly dependent on RNA synthesis. Unexpectedly this reorganization increases its rate in the absence of protein synthesis.     

Interaction between prostanoids and nitric oxide in the control of tubular function in rats with chronic bile duct ligation.

Recent work indicates that both nitric oxide and cyclooxygenase products play an important role in the renal alterations of liver cirrhosis, although the interactions between them have not been completely established. The purpose of this study was to assess the effect of simultaneous blockade of nitric oxide synthase and cyclooxygenase in rats with chronic bile duct ligation and in control, sham-operated rats. Compared with control rats, chronic bile duct ligation rats, 23-25 days after surgery, showed a decreased mean arterial pressure, natriuresis, and kaliuresis, without differences in glomerular filtration rate, and an increased urinary nitrite excretion. Nitric oxide synthesis inhibition by administration of N(G)-nitro-L-arginine methyl ester induced, in control rats, an increase in mean arterial pressure, without significant changes in natriuresis or glomerular filtration rate. In chronic bile duct ligation rats, N(G)-nitro-L-arginine methyl ester induced an increase in mean arterial pressure, natriuresis, and kaliuresis, together with a reduction in urinary nitrite excretion and an increase in prostaglandin E2 excretion. Cyclooxygenase inhibition with indomethacin induced in both experimental groups a marked inhibition in urinary prostaglandin E2 excretion without significant changes in Na+ or K+ excretion, and a significant increase in urinary nitrite excretion in control rats. N(G)-Nitro-L-arginine methyl ester in addition to indomethacin prevented the indomethacin-induced increase in nitrite excretion and dramatically reduced sodium excretion in both experimental groups. Thus, the present study suggests that both nitric oxide and cyclooxygenase products interact in the control of urinary sodium excretion and that each system is activated in the absence of the other one.     

A human skeletal muscle cell line obtained from an adult donor.

A cell line (RCMH) in permanent culture was established from surgically removed adult normal human skeletal muscle by exposure to conditioned media obtained from thyroid cells. Cells proliferated indefinitely but displayed density inhibition of growth while maintaining some differentiated markers. Under certain incubation conditions, cells fused into myotube-like structures, with a concomitant increase in muscle specific proteins, such as human myoglobin, skeletal muscle myosin, desmin and dystrophin, as identified using immunocytochemical procedures. In addition, RCMH cells displayed high affinity receptors for alpha-bungarotoxin (Bmax = 0.7 pmol/mg protein, Kd = 1.5 nM) and dihydropyridines (Bmax = 0.3 pmol/mg protein, Kd = 0.5 nM for [3H]PN200-110); these values are comparable to those reported for muscle cells in primary culture. Patch-clamp studies showed the presence of 42 pS carbachol gated channels and of 5 pS calcium channels (current carried by barium); chloride and potassium channels were also seen. This new cell line appears to be a convenient model system to study skeletal muscle function.     

Chromosome Numbers in Three Asteraceae Tribes from Inner Mongolia (China), with Genome Size Data for Cardueae

Chromosome counts are reported for 15 species of the family Asteraceae from Inner Mongolia (People’s Republic of China). This study includes representatives of the tribes Anthemideae (Artemisia, Chrysanthemum, Filifolium, Hippolytia and Neopallasia), Astereae (Heteropappus) and Cardueae (Echinops and Olgaea). The significance of the chromosome counts is discussed for each species. Within the Anthemideae, chromosome counts for Hippolytia alashanensis (2n?=?36) and the tetraploid level of Artemisia eriopoda (2n?=?36) are reported for the first time. The chromosome number of Heteropappus altaicus (Astereae) agrees with previous reports of one (4x) of the two ploidy levels reported for this taxon. As a complement to the karyological data, genome size of the Cardueae representatives was assessed using flow cytometry. Within this tribe, Echinops gmelini (2n?=?26) and its sister taxon E. acantholepis (2n?=?14) show strongly divergent karyological patterns of difficult interpretation, whereas the count of E. przewalskyi (2n?=?32), assigned here for the first time, coincides with those of its close relatives. In Olgaea tangutica, the chromosome count (2n?=?24) and genome size (2C?=?3.01 pg) given here are the first reports for both the species and the genus.     

Cytochemical localization of K(+)-dependent p-nitrophenyl phosphatase and adenylate cyclase by using one-step method in human washed platelets.

Ultrastructural cytochemical localization of ouabain-sensitive, potassium dependent p-nitrophenyl phosphatase (K(+)-NPPase) of the Na(+)-/K(+)-ATPase complex and adenylate cyclase (cAMPase) activities, in washed inactivated human platelets, are described. The one-step lead-citrate method, under similar incubation conditions, was used to determine both activities. K(+)-NPPase appeared in both plasma membrane and the surface-connected canalicular system (SCCS) of the platelets. These data suggest a uniform distribution of the enzyme throughout membrane systems which are in contact with the external medium. cAMPase activity was strictly localized in tubules of the dense tubular system (DTS) when incubation medium contained prostaglandin E1, prostaglandin D2 or forskolin, at concentrations known to stimulate the enzyme in platelets that are intact. This fact and the inhibition of cytochemical reaction by thrombin confirm that the one-step lead-citrate method is a useful procedure in determining adenylate cyclase, abolishing the unfavorable conditions of previously reported methods.     

A comparative study of the myoelectric amplitude characteristics for weight-holding tasks.

This study was conducted to examine the effects of load, time, and gender on five amplitude measures of the myoelectric signal (MES) for 10 male and 10 female subjects engaged in upper extremity weight-holding tasks. The results indicated that: (1) measures of amplitude variability (e.g.: standard deviation) are more sensitive to changes in load and time than the full-wave rectified integral and root-mean square indices; (2) both load and time had a significant effect on MES indices, suggesting that amplitude measures may be used as a tool for evaluating the degree of muscular loading and fatigue; (3) females have higher muscular exertion values than males under the same experimental conditions, indicating that females are subjected to higher levels of stresses than males for the same amount of workload. The implications of the results are discussed.     

Interaction sites of ruthenium red on the renal epithelium of Helix aspersa (Mollusca: Gastropoda)

The interaction sites of ruthenium red (RR) on the Helix aspersa renal epithelium are described. RR staining was located under septate junctions, at lamina densa of the basement membrane and in formations similar to intracytoplasmic vesicles and canaliculi. Digestive bodies and excretory spherules were also stained. The results are discussed in relation to the renal sac function.