Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UNIPROT:Q9UIJ5 (Rec)
 58,342 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The muscles of the pectoral girdle in domestic animals attach the forelimbs to the trunk and function as the suspensory apparatus. In the present study the composition of the pectoral girdle musculature of sheep by myofiber types was examined. Myofibers showing a strong reaction for alkali-stable myosin ATPase were classified into fast-twitch/glycolytic (FG) myofibers with a weak activity for NADH tetrazolium reductase (NADH-TR) and fast-twitch/oxidative/glycolytic (FOG) myofibers with a moderate and strong NADH-TR activity. Myofibers showing a weak reaction for alkali-stable myosin ATPase and a strong activity for NADH-TR were classified as slow-twitch/oxidative (SO) myofibers. The SO myofibers that showed a granular and striped pattern of diformazan deposits in NADH-TR activity were classified as SO-1 myofibers, whereas the SO myofibers characterized by a reticular pattern of diformazan deposits were classified as SO-2 myofibers. The trapezius, rhomboideus cervicis, and pectoralis descendens muscles situated superficially in the cranial regions of the back and chest had about 50% SO (SO-1 plus SO-2) myofibers. The deeply situated serratus ventralis cervicis and thoracis muscles had 37.5% SO myofibers. These five muscles included more SO-2 myofibers with large diameters than did all other muscles, and had about 50% and more cross-sectional area of SO myofibers. The other muscles had less than 32% SO myofibers and fewer SO-2 myofibers. The FOG and FG myofibers accounted for 50% or less in the muscles examined. Many muscles of the pectoral girdle had many fast-twitch (FOG plus FG) myofibers; they seem to meet locomotory requirements. In the pectoral girdle musculature, the SO myofibers were not necessarily distributed more in the deep regions than in the superficial regions.(ABSTRACT TRUNCATED AT 250 WORDS)
Anat Rec 1991 Jul
PMID:Composition of myofiber types in the pectoral girdle musculature of sheep. 183 Oct 13

Postural muscles have many type I myofibers, which reacted strongly for acid-stable myosin ATPase and were unreactive for alkali-stable myosin ATPase (Ariano et al., J. Histochem. Cytochem., 21:51-55, 1973; Armstrong et al., Am. J. Anat., 163:87-98, 1982; Smith et al., J. Neurophysiol., 40:503-513, 1977). House shrews (Suncus murinus) keep abducting their limbs in locomotion and hardly lift their trunk off the ground. The limb muscles of Suncus were examined by histochemical methods to determine whether the locomotory and postural behavior is related to the proportion of type I myofibers. The observation of whole cross sections from the triceps surae, flexor digitorum superficialis, quadriceps femoris, and caudally situated muscles in the thigh showed that all myofibers of these muscles were unreactive for acid-stable myosin ATPase and strongly reactive for alkali-stable myosin ATPase: Those were classified as type II myofibers. Type II myofibers showed a weak (type IIB), moderate (type IIAB), or strong (type IIA) reaction for NADH tetrazolium reductase. Part of type IIA myofibers reacted weakly to moderately for menadione-linked glycerol-3-phosphate dehydrogenase (m-GPD), which predominated in the soleus muscle. Type IIAB, type IIB, and the remainder of type IIA myofibers reacted strongly for m-GPD. The limb muscles contained subtypes of type II myofibers but no type I myofibers. In Suncus murinus, type I myofibers specialized for a postural maintenance may not be required because all myofibers function exclusively for propulsion.
Anat Rec 1990 Sep
PMID:Composition of myofiber types in limb muscles of the house shrew (Suncus murinus): lack of type I myofibers. 214 5

The composition of muscles by myofiber type is associated with their locomotory or postural functions. In the present study the composition of the hip and thigh musculature of sheep by myofiber types and the differences in their distribution were examined. Myofibers were classified into type I, IIA, and IIB myofibers by differences in myosin ATPase and NADH tetrazolium reductase (NADH-TR) activity. The vastus intermedius muscle consisted only of type I myofibers, which exhibit weak alkali-stable myosin ATPase and strong NADH-TR activity. The gluteus accessorius and profundus muscles had more than 50% type I myofibers. The other muscles had less than 50% type I myofibers as a whole. Type I myofibers were concentrated in the deep portions of the gluteus and quadriceps femoris muscles, which extend the hip and stifle joints, and of the pectineus muscle. They were scattered evenly in the caudally situated locomotory muscles in the thigh. Type IIA myofibers, characterized by strong alkali-stable myosin ATPase and NADH-TR activity, showed little difference in distribution in the hip and thigh muscles. Type IIB myofibers, characterized by strong alkali-stable myosin ATPase and weak NADH-TR activity, were distributed more in the cranial, caudolateral, and caudomedial portions than in the middle portions of the thigh. The distribution of type IIB myofibers is suited to powerful flexion and extension of the thigh and leg. In the hip and thigh musculature, it appears that type I myofibers are effectively distributed to maintain a standing posture without diminishing the propulsive force of the hindlimb.
Anat Rec 1988 May
PMID:Distribution of myofiber types in the hip and thigh musculature of sheep. 296 70

Isoflurane is an inhalational anesthetic agent associated with no known hepatic toxicity. Despite this fact, isoflurane has not been widely utilized as an anesthetic agent in studies of liver structure and function in experimental animals. For this reason, livers from rats treated with pentobarbital or diethylether were compared to those from rats treated with isoflurane to determine differences in biochemical and morphologic parameters. Liver from pentobarbital-treated rats showed a significant decline in glutathione-S-transferase activity compared to liver from isoflurane/O2 or ether-treated rats. Liver microsomes from isoflurane/O2-treated rats retained more cytochrome-C(P450)-reductase activity than did those from pentobarbital-treated, ether-treated, or decapitated rats. Despite these biochemical alterations, morphometric analysis of liver from isoflurane/O2 and pentobarbital-treated rats showed no quantitative or qualitative differences in liver structure or organelle volume densities. Neither were differences detected in uptake and distribution of 125I-epidermal growth factor when analyzed by electron microscopic autoradiography. These data show that isoflurane with supplemental O2 has no effects on hepatic structure and fewer effects on hepatic function than other anesthetics and may be a better experimental anesthetic than any currently in use.
Anat Rec 1987 Jun
PMID:Isoflurane as an anesthetic for experimental animal surgery. 361 78

Muscle biopsy samples were collected from the middle gluteal muscle of seven horses undergoing a nine-month endurance training programme. Samples were collected before the programme began and again after three, six and nine months of training. A fifth sample was collected three months after training ceased. Serial muscle sections were reacted histochemically for myosin adenosine triphosphatase after either acid (pH 4.3 and 4.6) or alkaline (pH 10.3) pre-incubation, and muscle fibres identified as type I, IIA, IIB or IIC. The oxidative capacity of individual fibres was assessed, using the reduced nicotinamide dinucleotide tetrazolium reductase stain, and the number of intermyofibrillar capillaries adjacent to each fibre was counted after staining, using the alpha-amylase periodic acid Schiff technique. Biochemical analyses involved the fluorometric measurement of the enzymes citrate synthase, 3-hydroxy acyl CoA dehydrogenase and lactate dehydrogenase as markers of end terminal oxidative, beta oxidative and glycolytic potential, respectively. There was an increase in the percentage of type IIB fibres having high nicotinamide dinucleotide tetrazolium reductase staining after three months training. This increase persisted throughout the period of training and during the period without training. There was an increase in the number of capillaries adjacent to type IIB fibres after six and nine months training. These had returned to near pre-training numbers after three months without training. There were increases in the activities of citrate synthase and 3-hydroxy acyl CoA dehydrogenase after three months training. The activities of both enzymes continued to rise throughout training and the highest activities were attained after nine months.(ABSTRACT TRUNCATED AT 250 WORDS)
Vet Rec 1987 Sep 19
PMID:Effects of a nine-month endurance training programme on muscle composition in the horse. 367 37

Cat intrafusal muscle fibers were examined histochemically in serial transverse sections of tenuissimus muscle spindles. The "myofibrillar" adenosine triphosphatase staining reaction was used to recognize the nuclear bag and the nuclear chain fibers in 309 spindle poles. Poles of 40 nuclear chain fibers extended for 1,000 micrometer or more beyond the termination of the spindle capsule. These long chain fibers stained less intensely for nicotinamide adenine dinucleotide tetrazolium reductase (NADH-TR) than the typical chain fibers of shorter polar length. In sections stained for cholinesterases (ChE), the extracapsular regions of most long chain fibers displayed one or two short, dense "plate"-type ChE deposits, which may represent the terminals of skeleto-fusimotor axons. In addition, about one-third of the long chain fibers displayed one or more thinner and smaller areas of ChE activity, possibly corresponding to the endings of fusimotor axons. The overall ChE staining pattern of the typical chain fibers was unlike that of the long chains. However, some of the shorter nuclear chain fibers resembled long chain fibers with the NADH-TR reaction, even though their ChE "plates" were located intracapsularly. It is concluded that nuclear chain fibers in the cat spindle form a class of intrafusal fibers with heterogeneous histochemical properties, and that the long chain fibers represent one fiber subtype.
Anat Rec 1980 Dec
PMID:Histochemical study of long nuclear chain fibers in the cat muscle spindle. 645 71

The endomembrane system in superficial and intermediate epithelial cells of mammalian urinary bladder was studied by cytochemistry, thin-section and freeze-fracture electron microscopy to determine the sites where special forms of membrane differentiation first appear. Glutaraldehyde-resistant NADH-ferricyanide reductase, distinctive 11-12 nm intramembrane particles (IMP), and asymmetry of membrane leaflets served as markers of membrane maturation. The three markers were specifically associated with the maturing face of Golgi apparatus and were absent from the remainder of the endomembrane system. Activity of this enzyme was associated with the lateral regions of the maturing face, fusiform vesicles, and the plasmalemma. Asymmetric unit membrane (AUM) plaques were not observed in the Golgi apparatus per se but were present in immature fusiform vesicles that had not detached from the maturing face. When freeze-fracture replicas and thin sections were compared, randomly arranged 11-12 nm IMP first appeared in maturing face membranes that were adjacent to clusters of "free" polyribosomes in the Golgi apparatus region. The proximity of these polyribosomes suggests that they may be related to the coincident appearance of the 11-12 nm IMP in the maturing face membrane. Our observations support the hypothesis that membranes undergo differentiation during "flow" through compartments of the endomembrane system. The lateral regions of the maturing face of the Golgi apparatus appear to be a critical location for the morphogenesis of plasma membranes in urinary bladder.
Anat Rec 1982 Aug
PMID:Membrane differentiation in the Golgi apparatus of mammalian urinary bladder epithelium. 713 97

Muscle cell fiber types in gracilis, rectus femoris, and long head of triceps brachii muscles of ferrets and dogs were identified on serial sections stained for myosin ATPase after preincubation at pH values of 9.8, 4.6, and 4.3 and for NADH-tetrazolium reductase (NADH-TR) activity. Although fiber types I and II were identified, the ATPase stain did not demonstrate classic type IIA/IIB fiber differences in either species. However, two type II fiber subtypes could be distinguished in the ferret because they differed slightly in staining intensity with ATPase at pH 4.3 and markedly with NADH-TR. One ferret type II fiber (designated II dark or IID) was smaller, slightly darker on ATPase, more oxidative on NADH-TR, and comprised more muscle volume than the other type II fiber (designated II light IIL). The IID fibers of ferret may represent the IID/X fibers of other authors. Both ferret type II fiber subtypes stained darker at pH 4.3 than canine II fibers. The NADH-TR staining indicated high oxidative activity in canine and ferret type I fibers. In contrast, type II fibers in the dog and IIL fibers in the ferret were moderately oxidative. Canine type IIC fibers were intermediate between type I and type II, whereas in the ferret, type IIC fibers were highly oxidative, as were type IID fibers. Ferret muscles are more oxidative than canine muscles according to NADH-TR staining. Also, ferret muscles possess 40-100% higher citrate synthase activity as compared to canine muscles.
Anat Rec 1993 Aug
PMID:Comparison of muscle cell fiber types and oxidative capacity in gracilis, rectus femoris, and triceps brachii muscles in the ferret (Mustela putorius furo) and the domestic dog (Canis familiaris). 769 Oct 36

We have studied the ability of the synthetic androgen methyltrienolone (R1881) to maintain testis and accessory organ weights, as compared to the effect of testosterone propionate (TP). In contrast to TP, R1881 is not metabolized and does not significantly bind to androgen-binding protein (ABP). Thirty-six rats were treated with ethane dimethane sulphonate (EDS) and GnRH antagonist (Org30267) to abolish all testicular androgen production, and recombinant human FSH (rec-hFSH, Org32489) was administered to ensure adequate FSH levels. Of these rats, five groups of four rats were treated daily with 0-, 50-, 100-, 200-, and 400-microgram TP, s.c., and four groups of four rats were treated daily with 150-, 300-, 600-, and 1200-microgram R1881, s.c. One control group of four rats received vehicle injections only. EDS treatment, followed by GnRH antagonist and rec-hFSH treatment for 17 days, significantly reduced testis, prostate, and seminal vesicle weights (P < 0.001, P < 0.01, P < 0.001, respectively). Simultaneous treatment with androgens prevented this organ weight decrease, in a dose-dependent manner. In all TP-treated animals, relative weights (% of control) of the acces, sory sex organs were significantly higher than the relative testis weights (P < 0.001). However, there was no difference in relative weights between testis and accessory sex organs in the R1881-treated animals. In another series of experiments, we investigated the effect of treatment with Finasteride, a 5 alpha-reductase inhibitor, on testis and accessory sex organ weights in rats treated with EDS and TP. Treatment with EDS, TP (300 micrograms/day) and Finasteride (40 mg/kg/day) did not alter testis weight as compared to the effect of treatment with EDS and TP alone. Prostate and seminal vesicle weights were, however, markedly reduced (significantly different from rats treated with EDS and TP alone; P < 0.01 and P < 0.05, respectively). Immunohistochemical analysis of androgen-receptor (AR) expression in the testis revealed that testicular AR immunoexpression is androgen dependent and that FSH alone is not able to maintain AR immunoexpression. Furthermore, the stage-dependent pattern of AR immunoexpression in Sertoli-cell nuclei, during the spermatogenic cycle, is identical in all TP- and R1881-treated rats. It is concluded that testes, prostate, and seminal vesicles are equally stimulated when the androgen receptor in these tissues is exposed to the same intracellular concentration of free androgen and that the low 5 alpha-reductase activity in the testis plays a critical role in the differential response of the testis and the accessory sex organs to T. Furthermore, stage-dependent AR immunoexpression in Sertoli cells does occur in the absence of testicular androgen production and is not due to androgen metabolism or local differences in androgen concentration.
 ...
PMID:Comparison of the response of rat testis and accessory sex organs to treatment with testosterone and the synthetic androgen methyltrienolone (R1881). 908 68

The inferior pharyngeal constrictor (IPC) muscle functions during swallowing, respiration, and vocalization. The most-caudal portion of the IPC is believed to be part of the functional upper esophageal sphincter (UES). We hypothesized that the caudal fibers of the human IPC may have enzyme-histochemical characteristics similar to those of the cricopharyngeus muscle, a major component of the UES. In this study, human IPC muscles obtained from autopsy were studied using Sihler's stain to examine innervation patterns, and using myofibrillar ATPase, NADH tetrazolium reductase (NADH-TR), and succinic dehydrogenase (SDH) techniques to investigate the distribution and oxidative capacity of the slow- (type I) and fast- (type II) twitch fibers in the muscle. The results showed that the human IPC consists of at least two neuromuscular compartments (NMCs): rostral and caudal. Each of the NMCs was innervated by a separate nerve branch derived from the pharyngeal branch of the vagus nerve. The rostral NMC is faster (39% type I, 61% type II) than the caudal NMC (70% type I, 30% type II). In addition, two histochemically-delineated fiber layers were identified in the human IPC: a slow inner layer (SIL) with predominantly type I fibers (66%), and a fast outer layer (FOL) with predominantly type II fibers (62%) (P < 0.01). However, the dimensions of both fiber layers and proportions of the muscle fiber types varied with the NMCs. Specifically, the ratio of the thickness of the SIL to FOL was approximately 2:1 for the caudal NMC and approximately 1:2 for the rostral NMC, respectively. In the SIL the type I fibers accounted for 84% for the caudal NMC and 69% and 44% for the lower and upper portions of the rostral NMC. In contrast, the type II fibers in the FOL accounted for 46% for the caudal NMC and 67% and 74% for the lower and upper portions of the rostral NMC, respectively (P < 0.01). The caudal NMC of the IPC shared histochemical characteristics with the cricopharyngeus muscle, in that it contained predominantly slow oxidative fibers. Overall, the caudal NMC and the SIL in the IPC had high NADH-TR and SDH activities. However, different patterns of oxidative enzyme activity were identified in both type I and type II fibers. This study provided histochemical evidence for the concept that the caudal NMC within the IPC contributes to the functional UES. In addition, the two histochemically-defined fiber layers in the IPC may be a specialized adaptation in humans to enable different upper-airway functions during respiration, swallowing, and speech.
Anat Rec 2001 12 01
PMID:Neuromuscular compartments and fiber-type regionalization in the human inferior pharyngeal constrictor muscle. 1174 92


1 2 Next >>