家兔与大鼠腓肠肌的生后发育比较

研究分析了家兔、大鼠腓肠肌在生后各年龄阶段的内侧头、外侧头的内侧亚体、中间亚体或外侧浅亚体、外侧亚体或外侧深亚体内快慢肌纤维的发育情况，应用大体解剖结合组织化学方法确定了其肌亚体，并进行琥珀酸脱氢酶染色、图像分析两型肌纤维的直径特征，以及肌构筑学与肌诱发电位的测量。结果表明：家兔在生后1个月时，内侧亚体从其深面凸现于内侧头与外侧亚体之间，中间亚体居于内侧亚体远端；大鼠内侧头未能区分肌亚体，其外侧头分为内侧亚体、外侧浅亚体，而外侧深亚体居于外侧浅亚体的深面呈重叠状：生后2、3天均未能分出Ⅰ、Ⅱ型肌纤维，也未见有原始肌束；Ⅰ、Ⅱ型肌纤维比例随年龄增长而变化，内侧亚体的Ⅱ型肌纤维比例在家兔与大鼠的生后发育中始终占优，而在其它各肌亚体内，Ⅱ型肌纤维的比例在发育中不恒定，直至成年后Ⅱ型肌纤维才趋于稳定并占优。在生长发育过程中，各肌亚体内Ⅱ型肌纤维的直径在各年龄段均大于Ⅰ型肌纤维。生后6个月家兔外侧头内侧亚体(FL／CSA)比值越大，倾向于速度型构筑；内侧头、中间亚体和外侧亚体(CSA／MW)比值越大，倾向于力量型构筑。大鼠腓肠肌外侧头内侧亚体乙酰胆碱酯酶染色显示葡萄状运动神经末梢支配慢肌纤维，斑点状运动终板位于快肌纤维。     

Ocular distribution of keratan sulfates during pre- and postnatal development in rabbits

Twenty-six monoclonal antibodies (MAbs) developed against rabbit corneal proteokeratan sulfate (PKS), were used to evaluate immunohistochemically the ocular distribution of PKS during prenatal and early postnatal development in rabbits. These MAbs were directed against epitopes located in the keratan sulfate (KS) chains of the proteoglycan (SundarRaj et al., 1985). Staining of cryostat sections of the eyes was carried out using an indirect peroxidase-conjugated technique. Only one of the MAbs reacted with the presumptive corneal region at day 13 or 16 of fetal development. By day 20, more MAbs reacted with the corneal stroma. There were distinct differences, however, in the distribution of the epitopes recognized by the various MAbs. A few of them stained only the posterior region of the cornea, whereas others showed a decreasing staining gradient from the posterior to the anterior region. By day 24, all of the MAbs reacted with the corneal stroma, but some reacted also with the limbal region and with the conjunctival stromal matrix. One MAb also reacted with the conjunctival epithelial layer, but only at this stage of development. Conjunctival staining was more intense at day 28 of fetal development and at day 2 postnatally. KS was not detectable in the conjunctiva of adult rabbits with any of the MABs. These results suggest that although KS synthesis starts at very early stages of fetal development, there are progressive changes in its antigenic structure in specific regions of the cornea and conjunctiva during corneal development.     

Electrophysiologic study of hippocampo-hypothalamic connections in rabbits

Using the evoked potentials (EP) studies have been made on functional connections of different fields (CA1, CA3) of the dorsal hippocamp with phylogenetically different parts of the hypothalamus in rabbits. It was shown that during stimulation of both the field CA1 and the field CA3 of the hippocamp, the EP are widely present in nuclear structures of the posterior hypothalamus (supramammilary area, the posterior hypothalamic area, mammilary bodies). In the anterior hypothalamus (area preoptic medialis), the EP were recorded only during stimulation of the field CA1 in the dorsal hippocamp.     

Neurophysiological analysis of the development of endocrine and hypertensive reactions in long-term emotional stress

A study was made of the effect of chronic emotional stress on the formation of hypertension in animals. This was shown to be related to dynamic changes in the function of the CNS, particularly in the hypothalamic apparatus of the neuroendocrine control. The above changes played a role in the formation of hypertensive vascular reactions accompanied by a high hormonal secretion of the adrenal cortex and thyroid. During stabilization of high arterial blood pressure at the late stages of the "after-effect", the hormonal secretion returns to normal.     

Morphometric studies of the postnatal development of the articular system of the bulbus oculi in rabbits

The postnatal development of oculo-motor reactions is probably caused partly by changes of the passive mechanical properties of the bulb joint system. The YOUNG's elasticity modulus seems to be a suitable parameter to describe these changes. For its calculation, the length and the cross section area of the extraocular muscles as well as the dimensions of the ocular bulb are necessary. Moreover, the bulb mass is needed to analyse the inertia of the bulb during each movement. The postnatal growth of these parameters was investigated and, by means of the linear regression analysis, we looked for the best fitted mathematical expression. By this, there is the possibility to estimate the morphological data for detailed longitudinal analysis of changes of the oculo-motor function if the age and the body mass, are known.     

Differential proteomic analysis of adrenal gland during postnatal development

The adrenal glands (AGs) are endocrine organs essential for life. They undergo a fetal to adult developmental maturation process, occurring in rats during the first postnatal month. The molecular modifications underlying these ontogenic changes are essentially unknown. Here we report the results of a comparative proteomic analysis performed on neonatal (Postnatal day 3) versus adult (Postnatal day 30) AGs, searching for proteins with a relative higher abundance at each age. We have identified a subset of proteins with relevant expression in each developmental period using 2‐DE and DIGE analysis. The identified proteins belong to several functional categories, including proliferation/differentiation, cell metabolism, and steroid biosynthesis. To study if the changes in the proteome are correlated with changes at the mRNA level, we have randomly selected several proteins with differential expression and measured their relative mRNA levels using quantitative RT‐PCR. Cell‐cycle regulating proteins (retinoblastoma binding protein 9 and prohibitin) with contrasting effects on proliferation are expressed differentially in neonatal and adult AG. Progesterone metabolizing enzymes, up‐regulated in the neonatal gland, might contribute to the hyporesponsiveness of the adrenal cortex characteristic of this developmental period. We have also observed in the adult gland a marked up‐regulation of enzymes involved in NAD(P)H production, thus providing the reducing power necessary for steroid hormone biosynthesis.     

Callosal connections in the cat parietal cortex during postnatal ontogenesis

By means of the method based on the retrograde axonal transport of horseradish peroxidase topography, quantitative and qualitative composition of homotopic neurons in the cat cerebral parietal associative cortex performing callosal connections have been studied. When comparing the data of the experiment with those previously obtained on distribution of the axonal terminals in the comissural neurons, certain places are revealed where concentration of the homotopic callosal connections of the parietal cortex field 7 take place. A morphological characteristic of the longaxonal pyramidal and stellate neurons forming these connections is presented.     

Studies of cardiac ganglia in pre- and postnatal rabbits

Summary This investigation was undertaken to describe the ultrastructure of cardiac ganglia in rabbits from day 18 of gestation to day 35 postpartum. Special attention was directed to the types of synaptic contacts made with the principal neurons and with the small granule-containing cells. The cardiac ganglia in all animals consisted mainly of parasympathetic postganglionic neurons, supporting cells, and small granule-containing (small intensely fluorescent) cells. The neurons received afferent synaptic terminals of two types. One type contained mainly small clear vesicles typical of most cholinergic terminals. The second type contained mainly small dense-core vesicles (these were most prominent after treatment of the animal with 5-hydroxydopamine), and were considered to be adrenergic terminals. These adrenergic terminals are probably part of an inhibitory system in the ganglia. The small granule-containing cells received typical afferent synaptic terminals of the cholinergic type, and also formed specialized contacts with certain axonal terminals. These latter specializations are considered to be reciprocal synapses which probably have a role in modulating ganglionic transmission.Supported by the Kentucky Heart Association and the Heart Association of Louisville and Jefferson County     

Quantitation of pulmonary neuroepithelial bodies in pre- and postnatal rabbits

Summary The size, density and total number of neuroepithelial bodies (NEB) in the lungs of late fetal, neonatal, and mature rabbits were determined using fluorescence microscopy. In this study lungs from 27-, 29-, 30-, and 31-day fetuses; neonates of ages 2, 7, and 30 days; and 4- and 7(+)-month-old rabbits, were used. The total number of NEB in the entire lung of rabbits from each age group was estimated based on measurements of collapsed lung volume, average NEB diameter, and NEB density (number/mm²). Average NEB diameter increased between 27 and 29 days gestation, then remained constant at 42–44 m between 29 days gestation and two days post-partum. Thereafter the diameter was significantly reduced in the 7-day group (33.7 m) and further reduced in the 4-month group (20.3 m). NEB density was initially high in 27-day fetuses (3.87/mm²), decreased significantly by 30 days gestation, increased to a high level by 2 days post-partum, then fell steadily, reaching the lowest level in the adult (0.15/mm²). This steady decrease in density was paralleled by a large increase in lung volume. The estimated total number of NEB in the lung was constant in all age groups except for a significant drop at 30 and 31 days gestation. These data indicate that the total number of NEB is maintained into adulthood; however, the density and average diameter of NEB decreases rapidly after 2 days postpartum. A sharp decrease in both total number and density observed under fluorescence microscopy at 30 and 31 days gestation suggests a change in NEB cellular activity just prior to birth.     

Quantitative analysis of postnatal myelin sheath development in the dorsal funiculus of rat

Postnatal development of myelin sheaths in the dorsal funiculus of rats has been studied qualitatively by light microscopy and morphometry. A distinction is made between Goll's tract and Burdach's tract, and, furthermore, inside Goll's tract the cervical, thoracic and lumbar areas are compared. The induction of myelinization is influenced by a critical range of axon thicknesses. Between the 15th and 20th days of postnatal maturation there is a minimal growth reaction in the dorsal funiculus, but after the 20th day up to the 120th day extensive growth of the myelin sheath can be seen. Burdach's tract shows earlier and faster development of the myelin sheath than Goll's tract cervically, which leads to the conclusion that epicritical sensitivity matures earlier in the upper extremity. Concerning Goll's tract in the lumbar area of the dorsal funiculus, faster maturation than in the thoracic and cervical areas can be seen.     

Perinatal development of mammillotegmental connections in rats

Development of direct axonal connections of the hypothalamic mammillary bodies with ventral and dorsal tegmental nuclei of Gudden was studied on fixed rat brains from day 14 of embryonic development until day 10 of postnatal development using the method of diffusion of the lipophilic fluorescent carbocyanine tracer 1,1′-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate along the neuronal membranes. The tracer was inserted into the mammillary bodies or into the tegmentum and, after incubation in a fixative, fluorescent nerve cells and nerve fibers were visualized in the brain tissue. The mammillotegmental tract was found to start developing earlier than other projection systems of the mammillary bodies. On days 14–15 of embryonic development, it was visualized as a bundle of axons running from the mammillary bodies caudally to the midbrain. A group of neurons in the midbrain tegmentum and their axons going to the mammillary bodies via the mammillary peduncle were first visualized on day 19 of embryonic development. The mammillotegmental tract and mammillary peduncle developed progressively from the moment of birth. Ventral and dorsal tegmental nuclei were formed in the midbrain by day 10 of the postnatal development. Thus, the formation of reciprocal connections of the mammillary bodies with midbrain tegmental nuclei was first described during perinatal development in rats.     

Perinatal development of mammillotegmental connections in rats

Development of direct axonal connections of the hypothalamic mammillary bodies with ventral and dorsal tegmental nuclei of Gudden was studied on fixed rat brains from day 14 of embryonic development until day 10 of postnatal development using the method of diffusion of the lipophilic fluorescent carbocyanine tracer 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate along the neuronal membranes. The tracer was inserted into the mammillary bodies or into the tegmentum and after incubation in a fixative fluorescent nerve cells and nerve fibers were visualized in the brain tissue. The mammillotegmental tract was found to start developing earlier than other conducting systems of the mammillary bodies. On days 14-15 of embryonic development, it was visualized as a bundle of axons running from the mammillary bodies caudally to the midbrain. A group of neurons in the midbrain tegmentum and their axons going to the mammillary bodies via the mammillary peduncle were first visualized on day 19 of embryonic development. The mammillotegmental tract and mammillary peduncle developed progressively from the moment of birth. Ventral and dorsal tegmental nuclei were formed in the midbrain by day 10 of the postnatal development. Thus, the formation of reciprocal connections of the mammillary bodies with midbrain tegmental nuclei was first described during perinatal development in rats.     

Mouse brain protein composition during postnatal development: an electrophoretic analysis

Changes in the concentrations of mouse brain proteins during postnatal maturation were characterized by a combination of subcellular fractionation and electrophoresis. Sodium dodecyl sulfate gel electrophoresis revealed changing protein concentrations in fractions enriched in nuclei, mitochondria plus synaptic endings, microsomes and cytosol. Postnatal maturational changes in protein concentrations were most pronounced in fractions of purified myelin membranes. The use of exponential gradient gels resulted in increased resolution of low molecular weight myelin proteins. Nuclei treated with Triton X-100 exhibited no change in relative histone concentrations during brain maturation. Nonnuclear contamination of untreated nuclear fractions was shown to be a potential source of erroneous interpretations. These findings are discussed in terms of genetic products and sodium dodecyl sulfate polyacrylamide gel electrophoresis resolution.