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ABSTRACT Background Aims Methods Results Conclusion Marionette lines are a feature of the aging face, descending from the oral commissures towards the jaw. VYC‐17.5 L is a dermal filler that contains 17.5 mg/mL of hyaluronic acid (HA) and lidocaine (3 mg/mL); it is intended for the treatment of skin depressions. VYC‐17.5 L has been shown to be safe and effective in different conditions, but there is a lack of published literature on its effectiveness in marionette lines.This 12‐month prospective, open‐label, post‐marketing study evaluated the effectiveness and safety of the injectable HA filler VYC‐17.5 L for the improvement of marionette lines.Adults (≥ 18 years) with mild‐to‐severe marionette lines on the validated Allergan Marionette Line Scale (AMLS) received VYC‐17.5 L on Day 1 with optional touch‐up on Day 14. The primary endpoint was proportion of participants with ≥ 1‐point change in AMLS from baseline at Month 1 (M1). Secondary endpoints were investigator‐ and participant‐rated Global Aesthetic Improvement Scale (GAIS), FACE‐Q satisfaction with facial appearance, and appraisal of lines: marionette. Safety was assessed throughout.A total of 83 participants completed the study; 69.9% of participants had ≥ 1‐point change in AMLS at M1. Investigator and participant GAIS showed improvement. Both FACE‐Q scores significantly improved from baseline (p < 0.0001). A significant volume improvement was seen and maximized at M1. Most participant‐reported injection site reactions were mild or moderate and resolved within 8 days; 14 subjects reported adverse device effects, with the most common being pain, which resolved within 8 days.This prospective, open‐label study showed that VYC‐17.5 L effectively improved marionette lines and was well tolerated. [ABSTRACT FROM AUTHOR]

Background: Macracantorhincosis is a zoonotic disease resulting from inadequate sanitary conditions, which occurs in pigs infected by acanthocephalic helminths called Macracanthorhynchus hirudinaceus. The eggs of these parasites are resistant to cold, high temperatures and can survive up to 3 years in the soil. They are consumed by dung beetles of the Scarabeidae family causing the parasite to evolve into its infective form, the cystacanth. The pig becomes infected after ingestion of either larvae or adult forms of these coleoptera. This work describes a case report of macracantorhincosis found in a pig from the canton of Zaruma located in the province of El Oro, Ecuador. Case: One sow, approximately 24-month-old, weighing 30 kg, presented cachexia, muscle weakness, pale oral and ocular mucosa and a body temperature above 39.4°C. The animal had a bulge on the ventral side of the neck, which evolved causing progressive discomfort to the point that the animal stopped eating. The sow was dewormed for 3 consecutive days. Fifteen days later, the animal had convulsions and muscle tremors, and died some hours after the symptoms started. During necropsy procedure, pale digestive tract membranes and nodules with fibrin were observed in the small intestine (jejunum), which was incised and the presence of parasites adhered to the granulomas detected. Two granulomas for morphological and histological studies and stool samples for coproparasitic test were collected. The collected parasites were fixed in a 10% buffered formalin solution, cross-sections were made and routinely processed for histological studies. The 5 μm thick sections were stained using the hematoxylin and eosin (HE) technique. The parasite’s action involves perforation of the intestinal wall though its proboscis causing peritonitis and enteritis. Other conditions in intestinal dissection such as necrotic areas, inflammation of the submucosa and adult parasites adhered to the intestinal mucosa were also observed. The coproparasitic examination was performed using the flotation and sedimentation techniques. The coproparasitic test detected dark colored feces, semi-solid consistency and the presence of Macracanthorhynchus hirudinaceu eggs. In the histological evaluation of the cross section of the parasite, the presence of circular and longitudinal muscle fibers and lemniscus with their constrictor muscles was observed. Cuticle, hypodermis with tapered fibers and a large number of developing mature eggs were also reported. Discussion: There is no pathognomonic symptomatology about this parasitosis and peritonitis can be generated by intestinal perforations. The findings at necropsy were ulcerations, inflammation in the small intestine and the presence of numerous nodules in the serous layer, where there was penetration of the parasite’s proboscis. When fixed to the mucosa, these parasites cause ulcerations, inflammation and necrosis in the wall of the small intestine. The hypodermic layer is thicker than the muscular layer and the presence of leminis with their constricting muscles are typical features of acanthocephalus. It is considered appropriate to carry out epidemiological studies on the prevalence of the parasite Macracanthorhynchus hirudinaceus at pig farming system in the region, in order to determine the main risk factors. In Ecuador, cases of this disease in humans have not yet been reported, but have already been described in other countries, so the presence of this parasite in family swine farming may be considered a zoonotic-type risk factor. [ABSTRACT FROM AUTHOR]

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The lack of a suitable flat epithelial preparation isolated directly from the freshwater fish gill has led, in recent years, to the development of cultured gill epithelia on semipermeable supports. To date, their minimal capacity to actively transport ions has limited their utility as ionoregulatory models. The current study describes a new method of culturing gill epithelia consisting either of an enriched population of pavement (PV) cells or a mixed population of PV cells and mitochondria-rich (MR) cells from the gills of adult rainbow trout. Although the cell culture approach is similar to the double-seeded insert (DSI) technique described previously, it makes use of Percoll density centrifugation to first separate populations of PV and MR cells, which are then seeded on cell culture supports in varying proportions on successive days so as to produce preparations enriched in one or the other cell types. Based on rhodamine staining, the MR cell-rich epithelia exhibited a threefold higher enrichment of MR cells compared to traditional DSI preparations. In general, MR cell-rich epithelia developed extremely high transepithelial resistances (TER; >30 kΩ cm2) and positive transepithelial potentials (TEP) under symmetrical conditions (i.e., L15 medium on both apical and basolateral sides). Apical exposure of cell cultures to freshwater reduced TER and produced a negative TEP in all the epithelial preparations, although MR cell-rich epithelia maintained relatively high TER and negative TEP for over 2 d under these asymmetrical conditions. Measurement of unidirectional Na+ fluxes and application of the Ussing flux ratio criterion demonstrated active Na+ uptake in PV cell-rich and MR cell-rich epithelia under both symmetrical and asymmetrical conditions. In comparison, Ca2+ uptake and Na+/K+-ATPase activity were significantly elevated in MR cell-rich preparations relative to the traditional DSI or PV cell-rich cultures under symmetrical conditions. This new methodology enhances our ability to tailor cultured gill epithelia on semipermeable supports with different proportions of PV cells and MR cells, thereby illuminating the ionoregulatory functions of the two cell types. [ABSTRACT FROM AUTHOR]

Mitochondria-rich cells (MR cells) of the gills of rainbow trout undergo changes in relative distribution and biochemical function during acclimation to partialstrength (10‰) and full-strength (30‰) seawater. In isolated total gill cells, Na+/K+-ATPase activity increased fivefoid and H+-ATPase activity decreased fourfold when trout were acclimated to either 10&permi;; or 30‰ seawater. When total MR gill cells were separated based on differential binding to peanut lectin agglutinin (PNA), the PNA subtypes underwent a change in relative distribution in seawater-acclimated fish. In freshwater, the ratio of PNA-:PNA+ was 65:35 while in seawater the distribution changed to 20:80 PNA-:PNA+. Additionally, differential changes in Na+/K+-ATPase and H+-ATPase activity in each of the independent cell types occurred during seawater acclimation; Na+/K+-ATPase activity in the PNA- cells increased by 197% while in PNA+ cells Na+/K+ATPase decreased by 57%. However, H+-ATPase activity was decreased in both PNA- (84%) and PNA+ (72%) subtypes during acclimation to seawater. [ABSTRACT FROM AUTHOR]

A novel cell isolation technique was used to characterize cadmium and calcium uptake in distinct populations of gill cells from the adult rainbow trout (Oncorhynchus mykiss). A specific population of mitochondria-rich (MR) cell, termed the PNA+ MR cell (PNA is peanut lectin agglutinin), was found to accumulate over threefold more 109Cd than did PNA- MR cells, pavement cells (PV cells), and mucous cells during a 1-h in vivo exposure at 2.4 microg/l 109Cd. In vitro 109Cd exposures, performed in standard PBS and Cl- -free PBS, at concentrations from 1 to 16 microg/l 109Cd, were also carried out to further characterize Cd2+ uptake kinetics. As observed during in vivo experiments, PNA+ MR cells accumulated significantly more 109Cd than did other cell types when exposures were performed by an in vitro procedure in PBS. Under such conditions, Cd2+ accumulation kinetics in all cell types could be described with Michaelis-Menten relationships, with Km values of approximately 3.0 microg/l Cd (27 nM) for both MR cell subtypes and 8.6 microg/l Cd (77 nM) for PV cells. In similar experiments performed in Cl- -free conditions, a significant reduction in 109Cd accumulation in PNA+ MR cells was seen but not in PNA- MR or in PV cells. In vitro 45Ca fluxes were also performed to determine the cellular localization of Ca2+ transport in these functionally distinct populations of gill cells. 45Ca uptake was most pronounced in PNA+ MR cells, with levels over threefold higher than those found in either PNA(-) MR or in PV cells. Results from the present study suggest that the PNA+ MR cell type is a high-affinity and high-capacity site for apical entry of Cd2+ and Ca2+ in the gill epithelium of rainbow trout.

A magnetic cell separation technique (MACS) was developed for isolating and characterizing peanut lectin agglutinin positive (PNA(+)) cells from rainbow trout gills. Percoll density separated mitochondria-rich (MR) cells were serially labeled with PNA-FITC and an anti-FITC antibody covalently coupled to a 50-nm iron particle and then applied to a magnetic column. PNA(+) MR cells were enriched to >95% purity. Transmission electron microscopy analysis of both the PNA(+) and PNA negative (PNA(-)) fraction showed that PNA binds to MR chloride cells while the PNA(-) cell fraction is comprised of MR cells with features characteristic of pavement cells. Western blotting demonstrated that both PNA(+) and PNA(-) fractions had high levels of Na(+)-K(+)-ATPase and Sco1 expression; however, relative expression of H(+)-ATPase in PNA(+) and PNA(-) cells demonstrated that untreated fish had twofold higher H(+)-ATPase levels in PNA(-) cells relative to the PNA(+) cells. Furthermore, hypercapnic acidosis significantly increased the relative H(+)-ATPase expression on PNA(-) cells only, whereas metabolic alkalosis had no significant effect.