Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Znaleziono wyników: 4

Liczba wyników na stronie
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 1 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników

Wyniki wyszukiwania

help Sortuj według:

help Ogranicz wyniki do:
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 1 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
INTRODUCTION: There are considerable differences in a number and density of muscle spindles in various skeletal muscles. Considerable sex differences in muscle mass and diameter of extrafusal muscle fibres suggest that muscle spindle density in muscles and morphometric properties of spindles: the diameter, the number and diameters of intrafusal muscle fibres are also different in males and females. Similar number of γ‑motoneurons in male and female rats suggest similar number of muscle spindles but their lower density in males. AIM(S): The aim of the study was to check sex differences in the number, the density and morphometric properties of muscle spindles in rat medial gastrocnemius muscle. METHOD(S): Medial gastrocnemius muscles were excised from two male and two female three-month old Wistar rats. Muscles were stored in 4% formalin solution and then cut into 10 and 20 µm slices stained with methylene blue and magenta. The light microscopy (Nikon microscope with camera and NIS Elements program) was used to calculate a number of muscle spindles in the muscle. The morphometric properties of spindles were measured on the equatorial regions. RESULTS: The number of muscle spindles is similar in male (13), in female (13–14) muscles. However, the density of spindles was different: 86–92 in males and 51–57 mg of the muscle mass per one spindle in females. There were also slight differences in a number of intrafusal muscle fibres in one spindle (in males: 4.3; range 3–8 and in females: 4.5; range 2–7). The diameters of intrafusal fibres on the equatorial regions amounted to: 6.7±2.1 µm in males and 6.6±2.6 µm in females. However, it was noticed that diameters of the male muscle spindles are larger than in the female ones: 21.4±7.3 µm and 20.2±5.7 µm, respectively. CONCLUSIONS: The main sex difference concerns density of muscle spindles which is lower in males than in females.
INTRODUCTION: There are numerous sex differences concerning male and female skeletal muscles, including muscle mass, the number and diameter of muscle fibers, and number of motor units; however, there is no data concerning the number and density of muscle spindles, which are the most important muscle proprioceptors. AIM(S): The experiments aimed to determine the number of gamma motoneurons, number and density of muscle spindles, as well as, their morphometric properties for rat medial gastrocnemius. METHOD(S): The motoneurons were stained with the horseradish peroxidase and neurons exceeding 27.5 µm were accepted as gamma size. Muscle spindles were counted in muscle cut into 5‑10 µm sections. The rat medial gastrocnemius was innervated by a similar number of gamma motoneurons (27.6±3.9 and 28.7±6.6, p>0.05) for female and males, respectively. RESULTS: However, size of gamma motoneurons was higher in males (23.5±2.9 µm) than in females (21.6±2.9 µm) (p<0.01). The number of muscle spindles amounted to 13.16±1.25 and 14.0±2.71 for female and males, respectively (p>0.05). The diameter of intrafusal muscle fibers was similar in males (5.16±2.43 µm) and in females (5.37±2.27 µm) (p>0.05), whereas the number of intrafusal muscle fibers was smaller in females (4.76±1.23) than in males (5.2±1.89, p<0.05). The mass of studied muscle was 61% higher in males (1.08 g vs. 0.66 g in females); therefore, the muscle mass per one spindle was 77 mg in males and 50 mg in females. CONCLUSIONS: The number of muscle spindles as well as their motor innervation by gamma motoneurons is similar in male and female rats, but the density of muscle spindles is considerably higher in females. FINANCIAL SUPPORT: Supported by grant 2018/31/ B/NZ7/01028.
INTRODUCTION: Carnosine (beta-alanyl-L-histidine) is predominantly present in skeletal muscle but also in other excitable tissues. It was suggested that muscle carnosine concentration can decrease with ageing. There is growing evidence that supplementation of carnosine can be effective for the treatment of age related disorders as well as neurological disorders e.g. Alzheimer’s disease or Parkinson’s disease. AIM(S): Here we investigate the effects of orally supplemented carnosine in aged rats on motor units (MUs) contractile properties. METHOD(S): 42 male Wistar rats aged 15 months were randomly assigned to three groups: control (CON; n=15), treated with carnosine for 8 months (CAR8M; n=15) or treated with lated and fixed. In one set of experiments the brains were frozen and cut with the use of cryotome. Then, slices were used either for Nissl staining to visualise anatomical structure, or in situ hybridisation for gene expression analysis. In another set of experiments, fixed brains were dissected into two hemispheres, after which a small DiI crystal was inserted into the thalamus. After incubation, the hemispheres were cut with a vibratome and DiI-stained axons were visualised under fluorescent microscope. RESULTS: We show here, that TCF7L2‑deficent mice displayed major changes in the anatomy of the thalamus and habenulae, as well as partial malformations of the striatum. Furthermore, Tcf7l2-/- mice most often completely failed to produce thalamocortical axons; if some were visible, they did not reach their cortical targets. CONCLUSIONS: The study demonstrated a critical involvement of TCF7L2 in thalamic nucleogenesis and establishment of thalamocortical axons. FINANCIAL SUPPORT: Work supported by NCN grants 2011/03/B/NZ3/04480 and 2015/19/B/NZ3/02949.
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 1 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.