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PubMed1996

An ultrastructural and lectin-histochemical study on the seminiferous epithelium of the common tree shrew (Tupaia glis).

The seminiferous epithelium of the common tree shrew (Tupaia glis) was investigated using transmission electron microscopy and lectin-histochemistry. It was compared with that of shrews examined in previous studies. Some peculiar structures were detected in the tree shrew spermatid at the electron microscopic level. The most characteristic feature was the disposition of mitochondria in early spermatids. In cap and early acrosome-phase spermatids, mitochondria accumulated in one area of the spermatid cytoplasm and then dispersed in the late acrosome phase. Subsequently they again clustered to form the middle piece of spermatozoa. While the lamellar structure was clearly seen in the caudal region of the spermatid nucleus, it gradually disappeared during the process of elongation. The dilated area in the postacrosomal space of early round spermatids was also characteristic. The dilation was not detected in elongated spermatids. These structures were not recognised in the seminiferous epithelium of shrews. With respect to lectin histochemistry, the binding patterns in the spermatid acrosome of the tree shrew were similar to those of the musk shrew. However, PNA and BPA, which reacted with the Sertoli cell cytoplasm of the musk shrew, showed no reaction in the tree shrew Sertoli cell. Thus, except for some lectin binding patterns in the spermatid acrosome, no close similarity was recognised in the morphology of the seminiferous epithelium between tree shrews and shrews.

Acrosome↗
PubMed1998

Muscle capillary supply in hind limb and diaphragm of the common shrew (Sorex araneus).

Shrew species of the subfamily Soricinae have unusually high metabolic rates when compared to Crocidurinae shrews and other similar-sized mammals. The aim of this study was to clarify whether the high basal metabolic rate of Soricinae shrews is reflected in a high capillary density in their muscles. To this end, the capillary supply of four limb muscles and diaphragm of the common shrew (Sorex araneus) was quantified from cross-sectioned muscles. The capillary densities of the limb muscles were 2575 +/- 329, 3111 +/- 299, 2812 +/- 197 and 2752 +/- 173 capillaries mm-2 fibre area in gastrocnemius lateralis, g. medialis, plantaris and soleus, respectively. Capillary density of the shrew diaphragm (6691 +/- 1057) was double that of the limb muscles. This value is among the highest ever measured in mammals. In general, the capillary supply in the hind limb of the common shrew is about 3-4 times higher than commonly found in the leg muscles of the laboratory rat or other bigger mammals, but similar to those in Crocidurinae shrews and some small rodents. Thus the high resting metabolism of the common shrew is not associated with an extraordinarily high capillary density. The apparent disparity between basal metabolic rate and muscle capillary supply in S. araneus is probably due to the small aerobic scope of shrews in the subfamily Soricinae.

Analysis of Variance↗
PubMed1996

Colon carcinogenesis in shrews by intrarectal infusion of N-methyl-N-nitrosourea.

Intrarectal infusion of a 0.15 ml solution containing 1.5 mg or 0.5 mg of N-methyl-N-nitrosourea (MNU) was given to female shrews from 6 weeks of age. Fifteen shrews were given 16 doses of 1.5 mg MNU administered biweekly (group 1), 15 shrews were given 24 doses of 0.5 mg MNU weekly (group 2), and four untreated shrews served as controls (group 3). Moribund shrews were killed during the course of the experiment and all remaining animals were killed at 37 weeks of age and terminated the experiment. The mean age when killed was 30.8 weeks in group 1 and 36.2 weeks in group 2. All autopsied shrews in group 1 and group 2, 13 shrews each, had colon cancers, and there were a few small intestinal cancers and uterine squamous cell carcinomas, while no tumors were seen in the untreated shrews. The colonic lesions were of both exophytic and endophytic type with a variety of histologies and depths of invasion. Mesenteric lymph node metastasis was seen in 31% (4/13) of group 1 and 23% (3/13) of group 2. Thus, MNU, a colonotrophic carcinogen in rodents, also induced colon cancer in shrews in the present study.

Administration, Rectal↗
PubMed1992

Maximum heart rate of soricine shrews: correlation with contractile properties and myosin composition.

Maximum heart rates (HR) of three soricine shrews and six other small mammals were measured in response to a single supramaximal dose of isoproterenol (Iso) under urethan anesthesia. The highest HR, 1,043 +/- 66 (SD) beats/min (n = 3), was in least shrew (Sorex minutus, mean body mass 3.02 +/- 0.81 g). Maximum HRs of common shrew (Sorex araneus, 7.16 +/- 1.54 g) and water shrew (Neomys fodiens, 12.80 +/- 1.54 g) were 938 +/- 29 (n = 7) and 887 +/- 21 (n = 6), respectively. In general, maximum HRs of soricine shrews and other small wild mammals followed the common mammalian pattern, fHmax/Iso = 443 x Mb-0.14, determined by body size. The exponent for this equation is smaller than that of resting HR (-0.25) (Stahl, J. Appl. Physiol. 22: 453-460, 1967), predicting crossover at approximately 3 g body mass. However, resting HRs of small mammals were clearly lower than expected on the basis of body mass. Lowering resting HR below the common mammalian level, with concomitant increase in stroke volume, seems to be a prerequisite for small mammals to regulate cardiac output against the ceiling of maximum HR. Electrophoretic analysis showed that the myosin of shrew ventricles is different from those of rodent species. In native conditions, shrew myosin, designated V1', migrated faster than the V3 and V1 forms of rat heart. On SDS gradient gel the single heavy chain of shrew myosin migrated slower than the alpha- or beta-chains of rat ventricle. Differences in the molecular weight of light chains were also noted between small mammals. Despite the notable differences in myosin composition, myosin-ATPase activity of the shrew hearts was similar to that of mouse and rat heart. Because duration of isometric contraction was inversely related to resting and maximum HRs, it was concluded that in the small mammals rate and duration of contraction are determined mainly by the release and uptake rate of myoplasmic Ca2+ and less by myosin-ATPase activity.

Animals↗
PubMed2004

[Unique structure of the esophago-gastric junction of the house musk shrew (Suncus murinus)].

The house musk shrew (Suncus murinus) belongs to the Order Insectivora, and has been used for the research in comparative anatomy as one of the most primitive placental mammals. Another feature of this shrew is its ability to easily vomit which mimics the human emesis or motion sickness response. The house musk shrew has thus been utilized as a rare small experimental animal for studies on the neurophysiological mechanism of vomiting. However, there is no report investigating the morphological background of vomiting in this species. The purpose of this study is to provide detailed morphological and histological features of the house musk shrew stomach as they possibly correlate to vomiting. The stomachs of ten female house musk shrews were used. Six of them were the wild type (Jic: SUN), two were the high-emesis strain (Jic: SUN-Her) and the rest of them were the low-emesis strain (Jic: Sun-Ler). In addition to the macroscopic anatomy, the region of esophago-gastric (EG) junction and the gastric groove were observed using the light and transmission electron microscopy. Although evident differences in structure of stomach were not found among the three strains, some interesting findings in comparative anatomy were noted. The circular valve-like thick fold was seen at the cardiac portion, which protruded into the esophageal lumen forming a deep groove between its frilled edge and the esophagus. The second frilled ridge was often found as inner ridge of this valve-like thick fold. The esophago-gastric junction between the stratified squamous and the simple columnar epithelium was found at the edge of the second frilled ridge. The lamina propria of the frilled edge was occupied by loose connective tissue and many large lumens of lymphatic vessels. The lamina muscularis mucosae, which developed in the esophageal region, was not in the main frilled edge. A well-developed inner muscle layer was found around the base of the fold, which seemed to correspond to the human lower esophageal sphincter. Cardiac glands occupied most of the thick cardiac wall, forming complicated crypts lined by simple columnar epithelium, and ducts of cardiac gland opened to these crypts. Since the house musk shrew has no esophageal gland, these cardiac glands may actively protect the lower part of the esophagus. In the cardiac wall, the inner circular and outer longitudinal muscle layer largely crossed each other obliquely as same as other reports. The transition area from the striated to the smooth muscle was observed in the sphincter surrounding the distal end of the cardiac wall. The gastric groove, lined by simple columnar epithelium in the lesser curvature, which has been reported to play a role as a shortcut from the cardia to the pylorus in other species including rodents, was also confirmed in the house musk shrew. The mucosal fold in the boundary between the esophageal and the gastric epithelium of house musk shrew may correspond to the structure called the limiting ridge (in mouse, rat and hamster), the teeth-like fimbria or Grenzfalten (in vole), and the gastric teeth (in crustacean and mollusk). The valve-like mucosal fold protruding into the esophageal cavity, the well developed huge cardiac glands, and the cardiac sphincter localized distally to the cardiac gland appear to facilitate the regurgitation of the stomach content, that is, vomiting. These findings suggest that this structure might have developed to support the feeding habit of house musk shrew, and that the differences of strains in vomiting may be determined by neurophysiological mechanisms.

Animals↗
PubMed1995

Fiber types and myosin heavy chain composition in muscles of common shrew (Sorex araneus).

Red-toothed shrews of subfamily Soricinae are small mammals with very high mass-specific metabolic rate. Owing to their high aerobic power they are interesting objects for studies concerning the limits and constraints of skeletal muscle adaptation. In order to clarify the correlation between metabolic rate and muscle properties, we have analyzed fiber types, fiber size, and myosin heavy chain composition of the common shrew (Sorex araneus) and compared them to those of rat (Rattus norvegicus). Three distinct differences between shrew and rat muscles were noted. 1) The fibers of shrew muscles are exceptionally small in comparison to rat myofibers. 2) Electrophoretic and histochemical analysis showed that shrew muscles are composed of only fast fibers (fiber types IIB and IID), the slow type I fibers being totally absent. 3) The shrew muscles are much more homogenous than rat muscles in regard to myosin heavy chain and fiber type composition. The shrew diaphragm consists exclusively myosin heavy chain type IId (MHCIId), while masseter and soleus are composed 95% and 87% of MHCIId, respectively. Other four studied muscles contain MHCIIb and MHCIId approximately in equal proportions. The present findings show that shrew muscles are composed of small, highly aerobic, fast type II fibers, which may be sufficiently fatigue-resistant to function both as postural muscles and to power fast and high frequency movements of limbs and diaphragm.

Animals↗
PubMed2004

Bioenergetics and thermal physiology of American water shrews (Sorex palustris).

Rates of O(2) consumption and CO(2) production, telemetered body temperature (T(b)) and activity level were recorded from adult and subadult water shrews (Sorex palustris) over an air temperature (T(a)) range of 3-32 degrees C. Digesta passage rate trials were conducted before metabolic testing to estimate the minimum fasting time required for water shrews to achieve a postabsorptive state. Of the 228 metabolic trials conducted on 15 water shrews, 146 (64%) were discarded because the criteria for inactivity were not met. Abdominal T(b) of S. palustris was independent of T(a) and averaged 38.64 +/- 0.07 degrees C. The thermoneutral zone extended from 21.2 degrees C to at least 32 degrees C. Our estimate of the basal metabolic rate for resting, postabsorptive water shrews (96.88 +/- 2.93 J g(-1) h(-1) or 4.84 +/- 0.14 ml O(2) g(-1) h(-1)) was three times the mass-predicted value, while their minimum thermal conductance in air (0.282 +/- 0.013 ml O(2) g(-1) h(-1)) concurred with allometric predictions. The mean digesta throughput time of water shrews fed mealworms (Tenebrio molitor) or ground meat was 50-55 min. The digestibility coefficients for metabolizable energy (ME) of water shrews fed stickleback minnows (Culaea inconstans) and dragonfly nymphs (Anax spp. and Libellula spp.) were 85.4 +/- 1.3% and 82.8 +/- 1.1%, respectively. The average metabolic rate (AMR) calculated from the gas exchange of six water shrews at 19-22 degrees C (208.0 +/- 17.0 J g(-1) h(-1)) was nearly identical to the estimate of energy intake (202.9 +/- 12.9 J g(-1) h(-1)) measured for these same animals during digestibility trials (20 degrees C). Based on 24-h activity trials and our derived ME coefficients, the minimum daily energy requirement of an adult (14.4 g) water shrew at T(a) = 20 degrees C is 54.0 kJ, or the energetic equivalent of 14.7 stickleback minnows.

Animals↗
PubMed1999

Defining the ancestral karyotype of all primates by multidirectional chromosome painting between tree shrews, lemurs and humans.

We used multidirectional chromosome painting with probes derived by bivariate fluorescence-activated flow sorting of chromosomes from human, black lemur (Eulemur macaco macaco) and tree shrew (Tupaia belangeri, order Scandentia) to better define the karyological relationship of tree shrews and primates. An assumed close relationship between tree shrews and primates also assists in the reconstruction of the ancestral primate karyotype taking the tree shrew as an "outgroup" species. The results indicate that T. belangeri has a highly derived karyotype. Tandem fusions or fissions of chromosomal segments seem to be the predominant mechanism in the evolution of this tree shrew karyotype. The 22 human autosomal painting probes delineated 40 different segments, which is in the range found in most mammals analyzed by chromosome painting up to now. There were no reciprocal translocations that would distinguish the karyotype of the tree shrew from an assumed primitive primate karyotype. This karyotype would have included the chromosomal forms 1a, 1b, 2a, 2b, 3/21, 4-11, 12a/22a, 12b/22b, 13, 14/15, 16a, 16b, 17, 18, 19a, 19b, 20 and X and Y and had a diploid chromosome number of 2n=50. Of these forms, chromosomes 1a, 1b, 4, 8, 12a/22a, and 12b/22b may be common derived characters that would link the tree shrew with primates. To define the exact phylogenetic relationships of the tree shrews and the genomic rearrangements that gave rise to the primates and eventually to humans further chromosome painting in Rodentia, Lagomorpha, Dermoptera and Chiroptera is needed, but many of the landmarks of genomic evolution are now known.

Animals↗
PubMed2006

Unique regulation of thyroid hormone metabolism during fasting in the house musk shrew (Suncus murinus, Insectivora: Soricidae).

The active hormone, 3,3',5-triiodothyronine (T3) is derived from thyroxine (T4) by the action of iodothyronine 5'-deiodinases (5'-D). By now two types of 5'-D have been identified; Type 1 (D1) and type 2 (D2). A relative contribution of these isotypes to the circulating T3 levels in the human remains to be determined whereas a number of reports indicate that, under physiological conditions, D1 plays a major role in maintaining circulating T3 levels in rodents. In both human and rodents, sickness and starvation reduce serum T3 concentration mainly through decrease in D1 activity. Recently, we found that the house musk shrew (Suncus murinus, Insectivora: Soricidae) has a different tissue distribution of D1 activity. Because compared to rodents D1 activity in the shrew was found only in liver at a much reduced level, D2 rather than D1 may play a role in the maintenance of serum T3. Therefore, we questioned how D1 and D2 activities change in fasted shrews and how these changes affect circulating thyroid hormone levels. We thus starved shrews for 24, 48 or 72 h and measured changes in serum concentration of T3, T4, and 3,3',5'-triiodothyronine (reverse T3, rT3) and D1 activities as well as its mRNA expression in liver. D2 activities were also measured in brown adipose tissue (BAT) and cerebral cortex of shrews. Unlike in human and rodents, T3 levels in shrews remained constant during fasting while T4 levels tended to decrease, resulting in an increase in its T3/T4 ratio. On the other hand, changes in rT3 levels were similar to those in human and rodents, being elevated with fasting. D1 mRNA and its activity were significantly reduced in the liver whereas D2 activities in BAT and cerebral cortex were increased by fasting. These results indicated that fasting in shrews also reduced hepatic D1 activity but it did not affect circulating T3 levels. The increased T3/T4 ratio together with increased D2 activity in BAT and cerebral cortex with fasting suggest that D2 rather than D1 is responsible for the maintenance of T3 levels in the house musk shrew.

Adipose Tissue, Brown↗
PubMed1997

The period of ovulation and presence of the first polar body of ova ovulated in the house musk shrew (Suncus murinus).

The period of ovulation in mature house musk shrews was examined in a natural mating group and a superovulation group treated with gonadotropin. In the natural mating group, ovulation started 14 hr after mating in 3 of the 7 house musk shrews (42.8%), and occurred in all 5 house musk shrews by 15 hr after mating. In the superovulation group, ovulation started 13 hr after the administration of hCG in 3 of the 5 house musk shrews, and was observed in all 5 shrews by 16 hr after the administration. In the natural mating group, ovulated ova were collected from the ovarian bursa of 14 house musk shrews 14-20 hr after mating (mean, 2.2 +/- 1.0 ova) and from the oviduct of 42 animals 14-24 hr after mating (mean, 3.6 +/- 1.8 ova). Among the ova ovulated 14-16 hr after mating, both mature ova with the first polar body and immature ova without the first polar body were observed. In the superovulation group, ovulated ova were collected from the ovarian bursa of 31 house musk shrews 13-22 hr after the administration of hCG (mean, 9.7 +/- 6.8 ova), and from the oviduct of 28 animals 13-24 hr after the administration of hCG (mean, 20.0 +/- 11.7 ova). There were also mature and immature ova in the ova ovulated 13-16 hr after the administration of hCG. The time when ova ceased to be recovered from the ovarian bursa roughly coincided with the time when new corpora lutea ceased to be found in the ovaries. These findings suggested that the period of ovulation of house musk shrews was 14-20 hr after mating in the natural mating group and 13-22 hr after the administration of hCG in the superovulation group. Both the natural mating group and superovulation group ovulated both mature ova with the first polar body and immature ova without the first polar body.

Animals↗
PubMed1987

Morphological and reproductive characteristics of musk shrews (Suncus murinus) collected in Bangladesh, and development of the laboratory line (BAN line) derived from them.

To establish a unique laboratory line of the musk shrew with different genetic properties from previously developed laboratory lines, 49 male and 49 female shrews were captured in the campus of Bangladesh Agricultural University from October through November in 1983 and from December in 1985 to January in 1986. The shrews collected were of various ages. They had light gray coats, with slight variations in color. Except for the 12 shrews introduced into our laboratory, the total length and body weight of the shrews ranged from 17.2 to 31.9 cm and 32.5 to 147.0 g in males, and 21.1 to 26.6 cm and 40.8 to 110.0 g in females, respectively. Pregnant females were found throughout the trapping period, and the average fetal litter size was 3.54 (11 cases). Five males and 7 females of the shrews captured in 1983 were transported to our laboratory. After more than 100 days of laboratory rearing, their total length and body weight averaged 27.6 cm and 147.3 g in males, and 24.6 cm and 81.7 g in females. Their body weight was more than double that of Japanese shrews. The shrews introduced (except for one male) produced a total of 59 offspring, which were regarded as the first generation of the laboratory line (BAN Line). Gestation period and average litter size were between 28 and 30 days (10 cases) and 3.47 (17 cases), respectively. The BAN line has consisted of about 60 individuals at each generation and has been maintained as a closed breeding colony.

Animals↗
PubMedDate not supplied

The fetal membranes of the otter shrews and a synapomorphy for afrotheria.

The otter shrews of mainland Africa are the closest relatives of the Madagascar tenrecs. We sought for similarities in placentation between the two groups and, in a wider context, with other mammals of the Afrotheria clade. Specimens of the Nimba otter shrew (Micropotamogale lamottei) were obtained from the Ivory Coast and examples of the giant otter shrew (Potamogale velox) from the Hill Collection. The Nimba otter shrew has a central haemophagous organ similar to that in tenrecs. The labyrinth of the Nimba otter shrew, however, is endotheliochorial with syncytial trophoblast enclosing the maternal vessels. On the other hand tenrecs have cellular haemomonochorial placentae and an associated spongy zone, which is not present in the Nimba otter shrew. The placenta of the giant otter shrew is also endotheliochorial. The central region of its placenta is particularly interesting, since the juxtafetal portion is clearly a haemophagous region whereas the labyrinth feeding this region is endotheliochorial. Thus there is considerable variation in placental morphology within Tenrecidae. Importantly, however, both otter shrews have a large allantoic sac divided into four intercommunicating lobes by two pairs of septal folds. A similar arrangement has been described for representatives of each of the remaining five orders within Afrotheria. This is significant because previous anatomical studies have failed to establish a single synapomorphy in support of Afrotheria.

Animals↗
PubMed2003

A cytoarchitectonic study of the hippocampal formation of the tree shrew (Tupaia belangeri).

Tree shrews constitute an interesting animal model to study the impact of stress or aging on the hippocampal formation, a brain structure known to be affected under such environmental or internal influences. To perform detailed investigations of the hippocampal formation, adequate knowledge of its anatomy should be present. Until now, the hippocampal formation of the tree shrew has not yet been studied extensively. The main objective of this study, therefore, was to describe the subfield boundaries in various levels of the dorsoventral hippocampal axis of the tree shrew (Tupaia belangeri) in detail. The secondary aim was to clarify whether a separate CA2 field can actually be distinguished in the tree shrew hippocampus, a fact that was denied in former reports. In addition, we aimed at investigating whether or not a CA4 subfield can be identified in the tree shrew's hippocampus. The immunocytochemical distribution of microtubule-associated protein 2 and the calcium-binding proteins, parvalbumin and calbindin, and the characteristics of Nissl staining in adjacent sections were compared. Because of the rather dorsoventral orientation of the long hippocampal axis in tree shrews, staining patterns were analyzed mainly in horizontal sections. The subiculum and the hippocampal CA1 and CA3 areas were easily identified. Moreover, we were able to demonstrate the existence of a distinct CA2 subfield in the tree shrew's Ammon's horn, contrary to previous reports. However, our results indicate that a CA4 field in the tree shrew hippocampal formation cannot be identified with the methods that we used. Therefore, supposed CA4 pyramidal neurons should be included into the CA3 field.

Animals↗
PubMed2006

Targeting of transmembrane protein shrew-1 to adherens junctions is controlled by cytoplasmic sorting motifs.

We recently identified transmembrane protein shrew-1 and showed that it is able to target to adherens junctions in polarized epithelial cells. This suggested shrew-1 possesses specific basolateral sorting motifs, which we analyzed by mutational analysis. Systematic mutation of amino acids in putative sorting signals in the cytoplasmic domain of shrew-1 revealed three tyrosines and a dileucine motif necessary for basolateral sorting. Substitution of these amino acids leads to apical localization of shrew-1. By applying tannic acid to either the apical or basolateral part of polarized epithelial cells, thereby blocking vesicle fusion with the plasma membrane, we obtained evidence that the apically localized mutants were primarily targeted to the basolateral membrane and were then redistributed to the apical domain. Further support for a postendocytic sorting mechanism of shrew-1 was obtained by demonstrating that mu1B, a subunit of the epithelial cell-specific adaptor complex AP-1B, interacts with shrew-1. In conclusion, our data provide evidence for a scenario where shrew-1 is primarily delivered to the basolateral membrane by a so far unknown mechanism. Once there, adaptor protein complex AP-1B is involved in retaining shrew-1 at the basolateral membrane by postendocytic sorting mechanisms.

Adherens Junctions↗
PubMed2004

Pressure-induced changes in axial eye length of chick and tree shrew: significance of myofibroblasts in the sclera.

PURPOSE: To investigate the change in axial eye dimensions resulting from stretching the sclera by acute elevation of intraocular pressure (IOP). METHODS: IOP was increased to 100 mm Hg for 1 hour through an intravitreal cannula, while ocular component dimensions were monitored every 10 minutes with A-scan ultrasound in anesthetized animals (10 chicks and 10 tree shrews). In addition, immunocytochemical detection of alpha-smooth muscle actin (alpha-SMA) using a monoclonal antibody was conducted in the sclera of the tree shrew and the chick. RESULTS: In both species, axial eye length immediately and significantly (P < 0.0001) increased on elevation of IOP to 100 mm Hg: chick to 103.9%, tree shrew to 101.2% (mean percentage of original measured at 15 mm Hg). After 1 hour of maintained pressure, chick eyes showed a further significant increase in axial length (to 108.6%), but axial length of tree shrew eyes decreased (to 100.3%) to the point that it was not significantly different from the original value at 15 mm Hg. Immunocytochemical studies of age-matched tissue demonstrated the presence of alpha-SMA-containing fibroblasts (myofibroblasts) within tree shrew but not chick sclera. CONCLUSIONS: Elevation of IOP caused axial elongation of chick eyes, but a consistent reduction in axial length of tree shrew eyes. The presence of myofibroblasts, demonstrated in tree shrew but not chick sclera, suggests that the reduction in axial length of tree shrew eyes may have been caused by activation of a contractile mechanism involving scleral myofibroblasts. Such a mechanism may play a role in the regulation of eye size and refractive development.

Actins↗
PubMed1996

The M1 muscarinic antagonist pirenzepine reduces myopia and eye enlargement in the tree shrew.

PURPOSE: To determine the efficacy of the M1-selective muscarinic antagonist, pirenzepine, in preventing experimentally induced myopia in a mammalian model, the tree shrew. METHODS: Tree shrews were monocularly deprived (MD) using translucent goggles or negative lenses for a period of 12 days. In two of the MD groups, tree shrews received daily subconjunctival administration of either pirenzepine (17.7 mumol; n = 9) or vehicle control (n = 6). Control groups (n = 6) were used to assess the effects of MD, injection regimen, and drug effects. RESULTS: In sham-injected and saline-injected MD tree shrews, 12 days of MD produced-13.2 D +/- 0.8 D and -14.1 D +/- 0.5 D of axial myopia, respectively. In pirenzepine-injected MD tree shrews, 12 days of MD induced an axial myopia of only -2.1 D +/- 1.4 D. The significant reduction in myopia in pirenzepine-injected MD tree shrews was caused by significantly less vitreous chamber elongation of the deprived eye (0.05 mm +/- 0.04 mm) relative to the contralateral control eye when compared to sham-injected and saline-injected MD tree shrews (0.24 mm +/- 0.02 mm and 0.29 mm +/- 0.01 mm). Mean equatorial enlargement and increased eye weight were prevented in pirenzepine-injected MD tree shrews (P < 0.01). Pirenzepine also was found to reduce myopia and ocular enlargement in lens defocus-induced myopia. Control experiments demonstrated that pirenzepine did not cause a significant reduction in amplitude of carbachol-induced accommodation. CONCLUSIONS: Findings demonstrate that chronic administration of the M1-selective muscarinic antagonist, pirenzepine, prevents experimentally induced myopia in this mammalian model by a nonaccommodative mechanism.

Accommodation, Ocular↗
PubMed2000

The transfer of lead (Pb) from earthworms to shrews (Myosorex varius).

Shrews (Myosorex varius) were bait-trapped close to Stellenbosch in the Western Cape, South Africa, and analyzed to determine the Pb content of the liver, kidneys, muscle tissue, brain, skull, and bone. Shrews were also fed in the laboratory on mince meat and Pb-contaminated live earthworms for 12-17 days and the Pb content compared with control shrews from the field. The Pb levels in the control shrews from the field were exceptionally high and exceeded levels generally considered to be critical for the onset of pathological symptoms in target organs. The shrews that were fed with Pb-contaminated earthworms had significantly higher Pb concentrations in their livers and kidneys than the control shrews. Given that Pb is bioaccumulated in earthworms, this study showed that predation on earthworms could constitute a major pathway for the entry of Pb into the food chain. M. varius could, similar to other species of shrews in other parts of the world, be a suitable biological monitor to study the environmental hazard of Pb pollution.

Animals↗
PubMed1994

Experimental accumulation of lead from soil through earthworms to common shrews.

Common shrews (Sorex araneus) were fed on earthworms containing high concentrations of lead. Both the earthworms and shrews originated from uncontaminated areas, but earthworms for the "lead" group of shrews were reared in the laboratory for 3 or 4 weeks in highly Pb-polluted soil from near an old lead smelter. The control group of shrews received the same amount of earthworms from the uncontaminated area. The acceptance of the experimental food by shrews was significantly lower in the lead group, indicating that the shrews were able to detect the lead in their food. After 2-31 days of feeding, the shrews in the lead group had significantly higher Pb concentrations in their liver, kidney, bone, and pelt than did the controls. Both the number of deaths during the experiment and the proportion of individuals with changes in kidney histology were significantly higher in the lead group.

Animals↗