Long-eared bats of the genus Plecotus are widespread over most of temperate Eurasia, marginally reaching the African continent and Macaronesia. Previously, all African populations were assigned to one species, P. auritus, and later to P. austriacus. We analysed museum specimens of African long-eared bat populations using both morphologic and genetic techniques. Based on morphological evidence we recognise four well-defined allopatric populations in northern Africa. They differ in fur coloration, skull morphology and bacular traits. The molecular data support a division of the African populations into at least three well-separated evolutionary lineages. With a combination of these data we define three species of Plecotus occurring in Africa (incl. the Canary Islands) and describe a new subspecies. Small, very pale greyish-brown Egyptian long-eared bats (P. christii Gray, 1838) inhabit desert and semi-deserts habitats of eastern Sahara (Libyan Desert, Nile Valley of Egypt and northern Sudan). Smaller to medium-sized, dark brown Ethiopian long-eared bats (P. balensis Kruskop et Lavrenchenko, 2000) inhabit the Ethiopian Highlands above 2000 metres a. s. l. This form represents the only Afro-tropical species of Plecotus. Large, dark greyish Canarian long-eared bats (P. teneriffae teneriffae Barret-Hamilton, 1907) occur on the three western islands of the Canarian Archipelago. A medium-sized greyish-brown Gaisler’s long-eared bat, P. teneriffae gaisleri subsp. n., is described from the Mediterranean region of Cyrenaica, north-eastern Libya. Due to the lack of substantial morphological differences we preliminarily consider the Maghrebian population of long-eared bats to be consubspecific with P. teneriffae gaisleri subsp. n. The systematic position of the population of Cape Verde Islands remains uncertain.
In this paper a combination of characters by which Poecilimon species (Orthoptera: Tettigonioidea: Phaneropteridae) can be recognised as members of the P. sanctipauli group are described. Most important are the wide fastigium, short ovipositor and song characters. The morphological characters are figured and described (Table 1), and the song patterns illustrated by oscillograms. The proposed phylogenetic relationships of the members of this group are written as [P. mytilenensis (P. pulcher, P. lodosi, P. sanctipauli)]. All species of the group are known from southwest Turkey and some east Aegean islands. The three species P. pulcher, P. lodosi and P. sanctipauli are morphologically and bioacoustically quite similar. P. sanctipauli and P. pulcher are distinct species, P. lodosi, however, possesses a combination of the key characters of the other two species. It may be a relict species or, in our opinion more probably, a species of hybrid origin.
The Neochauliodes sundaicus species-group is newly proposed, containing six species and endemic to Indo-Malaysia. All six species are described and illustrated, including two new species: Neochauliodes parvus Liu, Hayashi & Flint, sp. n. and N. peninsularis Liu, Hayashi & Flint, sp. n. Full species status is given to N. maculatus Stitz, 1914, stat. n. and N. borneensis van der Weele, 1909, stat. n. A cladistic analysis is conducted to reconstruct the species level phylogeny of the N. sundaicus group based on the morphological data. Combining the present morphological phylogeny and historical geography of Indo-Malaysia, the origin and speciation of this species-group is briefly discussed.
Cuckoos parasitize many rare and inconspicuous host species but avoid other common and conspicuous ones. In this article, results of a study that solved this long-standing ecological conundrum are described. I use this work to illustrate va - rious weaknesses of typical ecological studies (sample size, data representativeness, reification) and give suggestions for a better research practice in the future. and Jiří Klimeš, Ivan Literák.
The goal of this study is to evaluate if promotion of angiogenesis by systemic treatment with an antagomir against miR-92a, a well established inhibitor of angiogenesis, will maximize the benefits of exercise on bone. Ten week old female C57BL6/J mice were subjected to two weeks of external load by four point bending. During the first week of mechanical loading (ML), mice were injected (2.7 mg/kg of bodyweight) with antagomir against miR-92 or control antagomir (3 alternate days via retro-orbital). No difference in tissues weights (heart, kidney, liver) were found in mice treated with miR-92 vs. control antagomir suggesting no side effects. Two weeks of ML increased tibia TV, BV/TV and density by 6-15 %, as expected, in the control antagomir treated mice. Similar increases in the above parameters (7-16 %) were also seen in mice treated miR-92 antagomir. Administration of miR-92 antagomir was effective in reducing levels of mir-92 in heart, liver and skeletal muscle and in contrast, expression levels of two other microRNA’s miR-93 and miR-20a remain constant, thus suggesting specificity of the antagomir used. Surprisingly, we failed to detect significant changes in the expression levels of vascular genes (VEGF, CD31 and Tie2) in heart, liver or skeletal muscle. Based on these findings, we conclude that systemic administration of antagomir against miR-92 while reduced expression levels of miR-92 in the tissues; it did not significantly alter either angiogenic or osteogenic response, thus suggesting possible redundancy in miR-92 regulation of angiogenesis., A. Sengul, ... [et al.]., and Obsahuje seznam literatury
MiRNAs are important regulators of gene expression and changes in their levels are linked with various pathological states, including solid tumors. MiR-215 has been identified as a tumor suppressor in colorectal cancer (CRC). Following our previous in vitro and in vivo experiments, the aim of this project was to study the possibility of increasing the levels of miR
-215 in tumor cells by systemic administration of miRNA mimics in liposomal delivery system in vivo. By subcutaneous xenotransplantation of human cancer cells to NSG mice, CRC model was established.
The treatment [miR-215 mimics in liposomes (20 and 40 μg/mouse), control oligonucleotide in liposomes, or saline] was administered repeatedly by i.v. injection via tail-vein. Animals were sacrificed, tumor were dissected and measured by a caliper. Expression of miR-215 in tumors, lungs and liver was quantified by RT-PCR. There was no significant differences in tumor volume and miR-215 expression between all three treatment groups. Therefore, the decrease in tumor volume was
not achieved. By comparing the levels of miR-215 in lungs, liver
and tumors after the treatment, we suggest that the liposomes are accumulated in the lungs and do not concentrate sufficiently in the tumor site to exert significant tumor-suppressive effect.
The impact on blood pressure of two vasodilating mechanisms, underlied by vascular smooth muscle hyperpolarization, was studied and compared to that induced by nitric oxide (NO) mechanism. Systemic blood pressure, after inhibitory intervention in arachidonic acid metabolism (cytochrome P-450 inhibition by miconazole 0.5 mg/100 g b.w.), one of the hyperpolarizing pathways, did not change. After the inhibition of the action voltage-dependent K+ channels operator (by 4-aminopyridine 0.1 mg/100 g b.w.)
, the other hyperpolarizing pathway, blood pressure declined slightly (from 132.3±3.2 mm Hg to 116.5±5.0 mm Hg, P<0.05). Inhibition of nitric oxide production (L-NAME 5 mg/100 g b.w.) increased blood pressure considerably (123.5±2.7 mm Hg to 155.4±3.1 mm Hg, P<0.001). After inhibition of the hyperpolarizing pathway by miconazole, hypotension induced by acetylcholine (Ach, 10 μg) represented 63.0±1.9 mm Hg vs control value 78.6±5.2 mm Hg (P<0.001), by bradykinin (BK) (100 μg) 59.4±3.9 mm Hg vs control value 71.2±6.1 mm Hg (P<0.05). After inhibition of the hyperpolarizing pathway by 4-aminopyridine, hypotension induced by ACh (10 μg) achieved 64.6±2.5 mm Hg vs control value 78.4±2.8 mm Hg (P<0.001) and that induced by BK (100 μg)
56.6±5.3 mm Hg vs control value 72.3±2.5 mm Hg (P<0.001). ACh or BK hypotension after the inhibition of the above hyperpolarizing pathways was significantly attenuated. On the contrary, after NO-synthase inhibition the hypotension to ACh was significantly enhanced. Blood pressure decrease after ACh (10 μg) hypotension was 91.8±4.1 mm Hg vs control value 79.3±3.3 mm Hg (P<0.01), and after BK (100 μg) it was 78.4±7.1 mm Hg vs control value 68.3±5.2 mm Hg. A different basal BP response, but equally attenuated hypotension to Ach and BK, was detected after the inhibition of two selected hyperpolarizing pathways. In cotrast, the inhibition of NO production elicited an increase in systemic BP and augmentation of ACh and BK hypotension. The effectiveness of further hyperpolarizing mechanisms in relation to systemic BP regulation and nitric oxide level remains open.
The systemic effects of phytoecdysteroids were investigated by applying tested compounds to the roots of the rape plants. Evaluation of the effects was based on mortality, longevity, rate of development and fecundity of the cabbage aphid (Brevicoryne brassicae L., Sternorrhyncha: Aphididae) feeding on the shoot of the treated plants. The major ecdysteroid compounds tested were natural products isolated from a medicinal plant Leuzea carthamoides DC (Willd.) Iljin (Asteraceae): 20-hydroxyecdysone (20E), ajugasterone C (ajuC) and polypodine B (polyB). The compounds were tested in two concentrations (0.07 and 0.007 mg/ml) in water. In addition, we have also investigated the systemic effects of a special Lc-Ecdy 8 fraction isolated from L. carthamoides, which contained 20E, ajuC and polyB and at least six other minor compounds in addition to the above indicated ecdysteroids. HPLC analysis of the Lc-Ecdy 8 fraction indicated the presence of makisterone A and inokosterone in minor quantities. It appeared that all ecdysteroid compounds tested, with the exception of the most common, 20E, decreased the fecundity of cabbage aphids which fed on the contaminated rape plants. The mortality of larvae and adults significantly increased on plants treated with the Lc-Ecdy 8 fraction, and with ajuC or polyB compounds containing structural substituents in rather unusual positions. The most common phytoecdysteroid, 20E, with the typical and characteristic ecdysteroid structure, was the best tolerated of all phytoecdysteroids tested.