Activity-stress ulcer in the rat,hamster, gerbil and guinea pig

Rats, hamsters, gerbils and guinea pigs were housed in activity cages and fed 1 hr each day. By the end of the 21-day experimental period, 86, 100, 70 and 70% of rats, hamsters, gerbils and guinea pigs had developed lesions in the glandular stomach. This procedure was thus capable of producing lesions in species other than the rat, thereby increasing the value of the procedure as an ulcerogenic technique.     

Isolation has permanent effects upon the behavior of the rat,but not the mouse,gerbil, or guinea pig

In the rat isolation has both short-and long-term influences upon behavior. Rats isolated at any age will show increases in timidity and aggression, but both effects can be reversed by periods of social housing. However, isolation before 50 days of age has permanent effects upon behavior. We have previously found that rats between 25 and 45 days of age may be protected from the deleterious effects of isolation by short daily periods of social contact if, during these daily contact periods, the rats engage in intense bouts of rough-and-tumble play. In this study we examined the permanence of the effects of isolation on the rat, mouse, guinea pig and gerbil. As predicted by the play hypothesis, species which do not engage in extensive social play do not show permanent deficits if isolated prior to 50 days. Only rats which engage in long bouts of rough-and-tumble play between 20 and 50 days show any permanent behavioral effects of isolation during this period.     

The ultrastructure of the guinea pig rete testis

The chambers of the rete testis (RT) of guinea pig are lined by a simple epithelium, whose cells are squamous, cubical and columnar in shape. The epithelial cells with distinct shapes were counted and the quantitative analysis of the number of these cells showed relative predominance of cubical cells. The ultrastructural observations showed predominance of membrane interdigitations among the epithelial cells. These cells present common cytoplasmic organelles. The Golgi complex polarity is typical with observation of electronlucent vesicles on the Golgi cis face closely related to rough endoplasmic reticulum (ER) lamellae, mitochondria and large number of polysomes on the Golgi trans face. These related structures present in Golgi area of RT cells suggest secretory activity which maybe occurs in the RT epithelium. Endocytotic process also occurs in the RT and this function probably concerns the uptake of substances and resorption of seminiferous fluid. Apical cilia present in RT epithelium cells are related with fluid transport and perhaps with chemoreception. Presence of spermatozoa portions enclosed into the cytoplasm of some epithelium cells has been referred to as spermatophagy. The RT complex is mainly supported by loose connective tissue, with collagen fibres and some Leydig cells. Leydig cells are adjacent to the network channels of the septal part of the RT and apparently are able to secrete inside the RT lumen.     

Comparison of components of the testis interstitium with testosterone secretion in hamster,rat, and guinea pig testes perfused in vitro

Components of the testis and cytoplasmic organelles in Leydig cells were quantified with morphometric techniques in hamster, rat, and guinea pig. Testosterone secretory capacity per gram of testis and per Leydig cell in response to luteinizing hormone (LH) (100 ng/ml) stimulation was determined in these three species from testes perfused in vitro. Numerous correlations were measured among structures, and between structures and testosterone secretion, to provide structural evidence of intratesticular control of Leydig cell function. Testosterone secretion per gm testis and per Leydig cell was significantly different in the three species: highest in the guinea pig, intermediate in the rat, and lowest in the hamster. The volume of seminiferous tubules per gm testis was negatively correlated, and the volumes of interstitium. Leydig cell, and lymphatic space per gm testis were positively correlated with testosterone secretion. No correlations were observed between volumes of blood vessels, elongated spindle-shaped cells, or macrophages per gm testes and testosterone secretion. The average volume of a Leydig cell and the volume and surface area of smooth endoplasmic reticulum (SER) and peroxisomes per Leydig cell were positively correlated, and the volume of lysosomes and surface area of inner mitochondrial membrane per Leydig cell were negatively correlated with testosterone secretion. No correlations were observed between volume and surface area of rough endoplasmic reticulum (RER), Golgi apparatus, and lipid, and volume of ribosomes, cytoplasmic matrix, and the nucleus with testosterone secretion per Leydig cell. These results suggest that Leydig cell size is more important than number of Leydig cells in explaining the difference in testosterone-secreting capacity among the three species, and that this increase in average volume of Leydig cell is associated specifically with increased volume and surface are of SER and peroxisomes. An important unresolved question is what is the role of peroxisomes in Leydig cell steroidogenesis.     

Ultracytochemical and biochemical evidence for guanylate cyclase in guinea pig testis

Guanylate cyclase activity has been studied biochemically and cytochemically in guinea pig testis. The results of the biochemical assays indicate an equal distribution of this enzyme between the soluble and particulate fractions, which have a different sensitivity to adenosine triphosphate. The cytochemical results demonstrate that the reaction product of guanylate cyclase is detectable in the interstitial capillary endothelial cells and, in the seminiferous epithelium, mainly at the level of the adjacent surfaces of Sertoli and germ cells of the intermediate and adluminal compartments. Guanylate cyclase activity appears at the level of pachytene spermatocytes and persists throughout subsequent stages of development. The distribution in the seminiferous epithelium seems to indicate that guanylate cyclase is involved in the interrelationships between Sertoli and germ cells during gamete differentiation.     

锌缺乏导致小鼠睾丸游离锌离子和附睾精子数量减少

目的研究锌缺乏对小鼠睾丸游离锌离子和附睾精子数量的影响。方法锌缺乏饲养小鼠5周后,应用ZnSe金属自显影技术对小鼠睾丸和附睾进行染色,观察睾丸和附睾锌离子的分布,同时计数附睾精子数量,并与对照组小鼠的精子数量做对比。结果缺锌喂养后的小鼠睾丸游离锌离子明显减少,并且睾丸生精小管管腔狭小,生殖细胞层厚度增加,此外,附睾精子数量也明显低于对照组。结论睾丸和附睾内游离锌离子减少是锌缺乏小鼠精子数量下降的原因,本结果有助于改善男性生殖健康的状况。     

Cytochemical study on the distribution of adenylate cyclase in guinea pig testis

The distribution of adenylate cyclase in testis, by means of a specific substrate adenylyl-imidodiphosphate (AMP-PNP), has been determined. Membrane-associated reaction products, indicative of adenylate cyclase activity, are localized by a complete cytochemical medium (containing 10 mM NaF) at the level of the basal compartment of the seminiferous epithelium, on the basal surface of Sertoli cells, and on adjacent plasma membranes of Sertoli cells and spermatogonial cells. At the level of the adluminal compartment, reaction products were found on adjacent plasma membranes of Sertoli cells and early or elongated spermatids. Adenylate cyclase reaction products are detectable by a basal incubation medium (without 10 mM NaF) only in the adluminal compartment on the spermatid plasma membranes.     

Noradrenergic modulation of firing pattern in guinea pig and cat thalamic neurons, in vitro

1. The electrophysiological actions of norepinephrine (NE) in the guinea pig and cat thalamus were investigated using intracellular recordings from neurons of in vitro thalamic slices. 2. Application of NE to neurons of the lateral and medial geniculate nuclei, nucleus reticularis, anteroventral nucleus, and the parataenial (PT) nucleus resulted in a slow depolarization associated with a 2- to 15-nS decrease in input conductance and an increase in the slow membrane time constant from an average of 27.7 to 37.7 ms. The slow depolarization was not abolished by blockade of synaptic transmission, indicating that it was a direct (postsynaptic) effect. 3. The reversal potential of the NE-induced slow depolarization varied as a Nernstian function of extracellular potassium concentration ([K]o), indicating that it is due to a decrease in potassium conductance. This conclusion was supported by the finding that the amplitude of the NE-evoked depolarization was affected by changes in [K]o between 0.5 and 5.0 mM as expected for a K-mediated response. 4. Neurons of the PT nucleus displayed unusually large afterhyperpolarizations (AHPs) in comparison to cells in other thalamic nuclei. NE application to PT neurons caused not only a marked slow depolarization and decreased conductance, but also selectively reduced the slow AHP. 5. The NE-induced slow depolarization effectively suppressed burst firing and promoted the occurrence of single spike activity. NE-induced reduction of the slow AHP in PT neurons was accompanied by a decrease in spike frequency accommodation and the emergence of a slow afterdepolarization. 6. We suggest that through these electrophysiological actions, NE can effectively inhibit the generation of thalamocortical rhythms and greatly facilitate the faithful transfer of information through the thalamus to the cerebral cortex.     

Comparison of guinea pig cytomegalovirus and guinea pig herpes-like virus: growth characteristics and antigentic relationship.

The growth characteristics of guinea pig cytomegalovirus (GPCMV) and guinea pig herpes-like virus (GPHLV) in cell cultures were compared. Guinea pig fibroblast cells were highly susceptible to infection with both viruses, whereas guinea pig kidney cells were sensitive only to GPHLV. No cytopathic effect was observed in the latter cell system after infection with GPCMV,nor was there an increase in virus titer, although the cirus persisted in the kidney cells for 2 to 3 weeks postinfection. Electron microscope studies showed nonvirion tubular structures in GPCMV -infected fibroblast cells, but not in GPHLV- infected cells. Large packages of enveloped nuclear virus particles were commonly seen in GPHLV -infected cells, especially kidney epithelial cells, but none were found in the GPCMV -infected fibroblasts. Complete enveloped extracellular virus particles were present in both virus-cell systems. Both viruses showed narrow host spectra and replicated well only in guinea pig cells although GPHLV multiplied to some degree in rabbit cells. No antigenic relationship could be demonstrated between the two viruses using antisera specific for each virus that was produced in rabbits and guinea pigs. Rabbits produced high neutralizing antibody titers to GPHLV, whereas guinea pigs were the animals of choice for GPCMV antiserum production.     

Comparison of guinea pig cytomegalovirus and guinea pig herpes-like virus: pathogenesis and persistence in experimentally infected animals.

The pathogenesis of guinea pig cytomegalovirus (GPCMV) and guinea pig herpes-like virus (GPHLV) in guinea pigs was compared. Animals were inoculated with the two viruses by different routes and sacrificed after varying periods of time. GPCMV was consistently isolated from salivary gland 2 weeks postinoculation and thereafter following intraperitoneal or subcutaneous incoulaton. Virus was less frequently found in other tissues including blood, spleen, and kidney. Intranuclear inclusions were seen in tissue sections of salivary gland after inoculation with GPCMV- infected tissue suspension, but were only rarely found after inoculation with tissue culture virus. In GPHLV-infected guinea pigs, consistent latent infection of leukocytes and other tissues was detected by cocultivation techniques. Intranuclear inclusions were not found in the spleen, salivary gland, or other infected tissues after GPHLV infection with either tissue culture virus or infected tissue suspension. Guinea pigs inoculated with GPCMV produced high titers of specific neutralizing antibody to the homologous virus; those inoculated with GPHLV developed long-term viremia accompanied by minimal neutralizing antibody levels to the virus.     

Characterization of mononuclear phagocytes from the mouse,guinea pig,rat, and man

The present paper describes cytochemical, membrane, functional, and mitotic characteristics of monoblasts, promonocytes, monocytes, and macrophages of the mouse, guinea pig, rat, and man. For all of these species the results show that after staining for nonspecific esterase, with-naphthylbutyrate as substrate, and for lysozyme, mononuclear phagocytes can be distinguished from other cells, e.g., T and B lymphocytes. However, it must be kept in mind that immature and mature granulocytic cells are also lysozyme positive. The presence of Fc and C receptors is dependent on the maturity of the cells and the duration of incubation in vitro; with respect to the former, an in vivo population of immature mononuclear phagocytes may have a lower percentage of positive cells than is the case in a mature population, and with respect to the latter, the percentage of positive cells rises during incubation. Phagocytosis of opsonized bacteria and red cells is a reliable criterion for the distinction between mononuclear phagocytes and other cell types, e.g., lymphocytes and fibroblasts. In all of the species studied, the majority of both immature and mature mononuclear phagocytes ingested particles opsonized with IgG; the proportion of phagocytosis of red cells via C3 receptors is usually very small. Incorporation studies with [³H] thymidine have shown that immature mononuclear phagocytes (i.e., monoblasts and promonocytes) divide and that monocytes and macrophages do not. The small number of macrophages that incorporate [³H] thymidine are immature mononuclear phagocytes which have very recently arrived in the tissues from the bone marrow. Comparison of mononuclear phagocytes in different organs of various species has shown unequivocally that these cells belong to one cell line, called the mononuclear phagocyte system     

Studies of the guinea pig epididymis. II. Intercellular junctions of principal cells

The junctional complexes of the principal cells in the guinea pig epididymis were analyzed using freeze fracture and ultrathin section goniometric techniques. Replicas of the seven regions (I to VII) investigated reveal a continuous decrease in the number of tight junctional strands, ranging from 15.73 +/- 3.54 in zone I (proximal) to 4.39 +/- 0.78 in zone VII (distal tubule). The distance from the adluminal to the basolateral strand also diminishes from proximal, 0.73 +/- 0.02 micron to distal, 0.19 +/- 0.03 micron. The junctional strands appear on the P-face and anastomose forming compartments which are larger in the basolateral areas than those in the apical. The network of strands frequently form terminal loops and blind endings towards the more basal parts of the lateral membrane. Freeze fracture images also exhibit randomly distributed particulate aggregations which correspond to maculae adhaerentes, the highest number of which are found in zone IV, V, and VII. Desmosomal figures are found not only below, but also adjacent and intermingled among the tight junctional strands. This special junctional arrangement is confirmed upon goniometric analysis of ultrathin sections from zones IV, V, and VII. Electron dense desmosomal plaques are seen parallel and directly subjacent to the membranes of the tight junctions, following the strands in both directions to finally converge on the punctiform connections. Goniometry also reveals a dense feltwork of material closely applied along the lateral cell border. These zonulae adhaerentes are seen to be of greatest length and density in zones I, VI, and VII.     

The early pattern of cardiac innervation in the fetal guinea pig

Embryonic hearts were obtained from 78 guinea pig embryos at 20–40 days of gestation. They were frozen quickly, freeze-dried and prepared by the Falck catecholamine fluorescent method for demonstration of adrenergic fibers. Other hearts were fixed in 10% formalin and examined after silver impregnation with the Holmes technique. The results of the two methods were correlated to visualize the total neural pattern as well as the specific adrenergic elements of the developing hearts. The present study indicates that vagal fibers, accompanied by the primordia of the cardiac ganglia, reach the atrial wall on the twenty-fifth day of gestation in the guinea pig. They penetrate the wall and are distributed by individual branches throughout the atrial wall from days 26 to 29 inclusive. From day 30 to parturition, the basic pattern of atrial distribution is elaborated by the lengthening, thickening, and branching of individual fibers. Sympathetic fibers pass to the atrial wall from the twenty-fifth to twenty-ninth day, those coursing with the vagus nerve arriving on the twenty-fifth day, while the remaining fibers arrive on the twenty-sixth to the twenty-ninth days. A ventricular ground plexus of sympathetic fibers is present just deep to the epicardium on the twenty-sixth day, and from this point until 30 days of gestation the ground plexus penetrates the ventricular myocardial wall. The sympathetic fibers at first course along the edge of a muscle bundle, but not between muscle fibers. The nerves become thicker at 29 days but do not exceed 2 μ. They branch slightly at 27 days, and at 30 days they are well branched and appear to overlie the surface of the muscle bundles simulating a perimysial plexus. At 40 days a very dense perimysial plexus is visible which contains some fluorescent nerves. Complete autonomic innervation is established by the thirtieth day of gestation.     

Neuroleptic-induced changes in the firing pattern of guinea pig nigrostriatal neurons

Summary It is well established that neuroleptics increase the firing rate of nigrostriatal neurons. However, the action of these drugs on firing pattern has received scant attention. The effect of local administration of neuroleptic agents was investigated on the firing pattern, and also firing rate, of nigro-striatal neurons. Chlorpromazine or haloperidol was microinjected into the substantia nigra of the urethane-anaesthetized guinea pig during extracellular recordings from identified nigrostriatal cells. Both neuroleptics induced the familiar increase in firing rate of nigrostriatal neurons. More significantly, however, these drugs also caused a dose-dependent change in firing pattern, specific to neuroleptic action. This change consisted of a drug-induced transition from slow irregular single or double spikes with a short interspike interval (beat firing) to irregular bursts of spikes with a longer interspike interval (burst firing). Furthermore, the transition from beat to burst firing occurred sharply and sometimes continued to switch in a regular cyclical fashion between the two modes for up to three hours following infusion of the neuroleptic. Administration of neuroleptics may thus provide a useful tool for studying the physiology of the firing pattern of nigrostriatal neurons.     

Degenerated tubules in the guinea pig testis after long-term vasectomy or sham operation

The testes of eight unilaterally vasectomized and six sham-operated Dunkin Hartley guinea pigs were examined 3 years after operation by wax and resin histology and transmission electron microscopy. Degenerated tubules are reported that were common on the side of vasectomy but also found in the contralateral testes and in the controls. A central accumulation of macrophages, rich in phagocytosed debris including spermatozoal fragments, was surrounded by attenuated Sertoli cells, a markedly thickened basement membrane and myoid cells. At some sites macrophages impinged directly on the basement membrane. They probably represented highly degenerated seminiferous tubules. The study suggests that the response to injury of seminiferous tubules may show species variations. Macrophages did not feature in the degenerated seminiferous tubules we reported following vasectomy in the rat. However, the rat showed striking changes in the morphology of the basal laminae and myoid cells which did not occur in the guinea pig. Pathological changes have been reported in the human testis following vasectomy but their etiology is unclear. Studies in the guinea pig are enhancing understanding of the mechanisms and features of testicular damage.     

Microassay for colorimetric estimation of complement activity in guinea pig,human and mouse serum

A sensitive colorimetric microassay for determining haemolytic complement activity was devised. It is carried out in U-welled microtitre dishes covered with plastic tape, which are incubated in a waterbath and subsequently centrifuged. The supernatant is transferred to flat-bottomed microtitre dishes and haemolysis is estimated by automatic measuring of the absorption using an interference filter of 405 nm in a Titertek Multiskan. Advantages of the method described are saving time and materials, and avoiding the use of radioactive nuclides. This microassay may therefore be a useful substitute for macro and semi-macro tests for colorimetric determination of serum complement activity and for microassays based on the release of a radio-isotope.