Beurteilung der Lungengesundheit von Schweinen aus verschiedenen ökologischen Haltungssystemen mittels BAL und Lungenhistologie

Im vorliegenden Forschungsvorhaben wurde die Lungengesundheit von Schweinen in Abhängigkeit von verschiedenen Haltungs- und Managementbedingungen beschrieben. Die Untersuchung erfolgte an Mastschweinen verschiedener Herkünfte (konventionell – ökologischer Tiefstreustall – Stall nach EU-Öko-VO – Freilandhaltung) und an Tieren unterschiedlichen Alters. In der konventionellen Schweinemast handelte es sich hierbei um Ferkel, Läufer und Mastschweine derselben Herkunft, in der ökologischen Schweinemast um Läufer, Mastschweine und XXL-Schweine von jeweils zwei Beständen. Letztere Untersuchung diente vor allem der Abbildung möglicher Effekte von Unterschieden im betrieblichen und Hygienemanagement auf die Tiergesundheit in den beiden ökologischen Beständen. Der Gesundheitszustand der Tiere mit Betonung des Lungenbefundes wurde über Schlachtkörperuntersuchungen, bronchoalveoläre Lavage (BAL) und histologische Untersuchung makroskopisch auffälliger Lungenbefunde erfasst. Allgemein wurde festgestellt, dass die Tiere im Zeitverlauf und in Abhängigkeit von den Haltungsbedingungen Zeichen einer zunehmenden entzündlichen Veränderung im Bereich der Atemwege zeigten (BAL: prozentuale Reduktion der Makrophagen bei gleichzeitigem relativen Anstieg der Lymphozyten). Die histologische Untersuchung wies auf ein unterschiedlich ausgeprägtes v.a. viral bedingtes infektiöses Geschehen hin, das möglicherweise durch eine in unterschiedlichem Ausmaß bestehende irritative Schädigung der Atemwege gefördert wurde. Sowohl bei Untersuchung der Mastschweine als auch bei Probenahme bei unterschiedlich alten Tieren wurde deutlich, dass den Managementfaktoren (Entwurmung, Impfstatus, Hygiene) eine bedeutende Rolle im Hinblick auf den Gesundheitszustand zukommt. Im negativen Fall führte dieser Effekt dazu, dass die Anzahl auffälliger Befunde trotz vergleichsweiser guter Stallluftqualität (sehr) hoch war. Neben baulich-technischen Faktoren kommt folglich dem Management eine sehr große Bedeutung zu

Fragen des Arbeits-, Tier- und Umweltschutzes bei der Schweinemast in verschiedenen Systemen unter besonderer Berücksichtigung mikrobieller Belastungen

Vor dem Hintergrund häufiger Atemwegserkrankungen bei Schweinen und landwirtschaftlich Beschäftigten war es das Ziel eines interdisziplinären Verbundprojektes, Belastungen von Mensch, Tier und Umwelt in ökologischen und konventionellen Haltungssystemen für die Schweinemast zu erfassen. Die Untersuchungen wurden in zwei konventionellen (Stall A, B) (BVT-Stall, 50% reduzierter Schlitzanteil, Zwangsbelüftung) und zwei ökologischen Ställen durchgeführt: Stall C (Praxisstall: Tiefstreu, freie Fenster-Lüftung), Stall D (Praxisstall: EU-Öko-VO, Trauf-First-Lüftung). Über 2 Mastperioden (je 3 Messungen; kalte / warme Jahreszeit) wurden die Parameter erfasst: luftgetragene Endotoxine, Schimmelpilze, Bakterien mit Differenzierung, arbeitsmedizinische Staubfraktionen, Materialproben, Staubfraktion PM10, NH3, CO2 und CH4, Lufttemperatur, Luftfeuchte. Die Beschreibung der Tiergesundheit erfolgte über serologische (Mycoplasmen, PRRS-, Influenza-A- und Circo-Virus) und koprologische (Parasitenbefall) Analysen und über Schlachtkörper- und Organbefundungen (Lunge, Pleura, Perikard, Leber). Am Beispiel der Endotoxin-Konzentration wurden die z.T. sehr hohen biologischen Belastungen deutlich: Stall C (Median: 14.495 EU/m3), Stall A/B (5.544 EU/m3), Stall D (2.876 EU/m3). Personengetragene Messungen führten zu deutlich höheren Werten. Die CO2- und NH3-Konzentrationen lagen in allen Ställen im Durchschnitt deutlich unter dem Grenzwert von 3000 ppm bzw. 20 ppm. In Stall C und D war die CH4-Konzentration allerdings höher als in Stall A/B (oberer Bereich der Literaturangaben). Auffällige Lungenbefunde fanden sich bei ca. 45% der untersuchten Schlachttiere, unabhängig vom Haltungssystem; parasitäre Leberveränderungen wurden ausschließlich in den Ställen C und D ermittelt. Die Untersuchungsergebnisse unterstreichen die Bedeutung der Ausführung, Dimensionierung und Regelung des Lüftungssystems sowie die Sauberkeit bzw. Hygiene und insbesondere das Betriebsmanagement im Stall und ihre Schlüsselrolle hinsichtlich der Freisetzungsmengen von Schadstoffen sowie der Tiergesundheit. Demgegenüber kommt der Klassifizierung der Haltungsumwelt durch die Einteilung in Haltungssystemen nur eine geringe Aussagekraft zu

Исследование влияния температуры на процесс восстановления ацетилдифенила изопропилатом алюминия

We present a compact module, emitting nearly diffraction limited green laser light at 531 nm at an average output power of more than 500 mW. As pump source for the second harmonic generation a DBR tapered laser with a total length of 6 mm was used. The RW section had a length of 2 mm including a 1 mm long passive DBR section. The devices were mounted p-side up on a copper block. For this mounting scheme, the device reaches up to 7 W maximal output power. At the power level of about 3.8 W used in the presented experiment, a wavelength of 1062.6 nm with a line-width below 0.02 nm (FWHM) was determined. More than 80% of the emitted power is originated within the central lobe of the beam waist profile illustrating the nearly diffraction limited beam quality. Using a 30mm long MgO-doped periodically poled LiNbO3 bulk crystal, the second harmonic wave is generated in a single-pass setup. Due to precise alignment and beam shaping based on the results of numerical simulations and a properly temperature control of the PPLN crystal, a maximum optical conversion efficiency of more than 14% (3.7%/W) was achieved. The fluctuation of the output power is far below 1%

Rhabdomyolysis: a genetic perspective

Rhabdomyolysis (RM) is a clinical emergency characterized by fulminant skeletal muscle damage and release of intracellular muscle components into the blood stream leading to myoglobinuria and, in severe cases, acute renal failure. Apart from trauma, a wide range of causes have been reported including drug abuse and infections. Underlying genetic disorders are also a cause of RM and can often pose a diagnostic challenge, considering their marked heterogeneity and comparative rarity.In this paper we review the range of rare genetic defects known to be associated with RM. Each gene has been reviewed for the following: clinical phenotype, typical triggers for RM and recommended diagnostic approach. The purpose of this review is to highlight the most important features associated with specific genetic defects in order to aid the diagnosis of patients presenting with hereditary causes of recurrent RM

Multi-minicore Disease

Multi-minicore Disease (MmD) is a recessively inherited neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy. Prevalence is unknown. Marked clinical variability corresponds to genetic heterogeneity: the most instantly recognizable classic phenotype characterized by spinal rigidity, early scoliosis and respiratory impairment is due to recessive mutations in the selenoprotein N (SEPN1) gene, whereas recessive mutations in the skeletal muscle ryanodine receptor (RYR1) gene have been associated with a wider range of clinical features comprising external ophthalmoplegia, distal weakness and wasting or predominant hip girdle involvement resembling central core disease (CCD). In the latter forms, there may also be a histopathologic continuum with CCD due to dominant RYR1 mutations, reflecting the common genetic background. Pathogenetic mechanisms of RYR1-related MmD are currently not well understood, but likely to involve altered excitability and/or changes in calcium homeoestasis; calcium-binding motifs within the selenoprotein N protein also suggest a possible role in calcium handling. The diagnosis of MmD is based on the presence of suggestive clinical features and multiple cores on muscle biopsy; muscle MRI may aid genetic testing as patterns of selective muscle involvement are distinct depending on the genetic background. Mutational analysis of the RYR1 or the SEPN1 gene may provide genetic confirmation of the diagnosis. Management is mainly supportive and has to address the risk of marked respiratory impairment in SEPN1-related MmD and the possibility of malignant hyperthermia susceptibility in RYR1-related forms. In the majority of patients, weakness is static or only slowly progressive, with the degree of respiratory impairment being the most important prognostic factor

Effect of aerobic exercise on waist circumference in adults with overweight or obesity : a systematic review and meta-analysis

Excess visceral adiposity contributes to elevated cardiometabolic risk, and waist circumference is commonly used as a surrogate measure of visceral adipose tissue. Although regular aerobic exercise is known to improve abdominal obesity, its effect on waist circumference is unclear. A systematic review and meta-analysis was performed to determine (1) the effect of aerobic exercise on waist circumference in adults with overweight or obesity; (2) the association between any change in waist circumference and change in visceral adipose tissue and/or bodyweight with aerobic exercise interventions; and (3) if reductions in waist circumference with exercise are moderated by clinical characteristics or components of aerobic exercise prescription. Twenty-five randomized controlled trials (1686 participants) were included. Regular aerobic exercise significantly reduced waist circumference by 3.2 cm (95% confidence interval [CI] −3.86, −2.51, p ≤ 0.001) versus control. Change in waist circumference was associated with change in visceral adipose tissue (β = 4.02; 95% CI 1.37, 6.66, p = 0.004), and vigorous intensity produced superior reduction (−4.2 cm, 95% CI −4.99, −3.42, p < 0.0001) in waist circumference compared with moderate intensity (−2.50 cm, 95% CI −3.22, −1.79, p = 0.058). These findings suggest regular aerobic exercise results in modest reductions in waist circumference and associated visceral adipose tissue and that higher intensity exercise may offer superior benefit to moderate intensity

Respiratory features of centronuclear myopathy in the Netherlands

Centronuclear myopathy (CNM) is a heterogeneous group of muscle disorders primarily characterized by muscle weakness and variable degrees of respiratory dysfunction caused by mutations in MTM1, DNM2, RYR1, TTN and BIN1. X-linked myotubular myopathy has been the focus of recent natural history studies and clinical trials. Data on respiratory function for other genotypes is limited. To better understand the respiratory properties of the CNM spectrum, we performed a retrospective study in a non-selective Dutch CNM cohort. Respiratory dysfunction was defined as an FVC below 70% of predicted and/or a daytime pCO2 higher than 6 kPa. We collected results of other pulmonary function values (FEV1/FVC ratio) and treatment data from the home mechanical ventilation centres. Sixty-one CNM patients were included. Symptoms of respiratory weakness were reported by 15/47 (32%) patients. Thirty-three individuals (54%) with different genotypes except autosomal dominant (AD)-BIN1-related CNM showed respiratory dysfunction. Spirometry showed decreased FVC, FEV1 &amp; PEF values in all but two patients. Sixteen patients were using HMV (26%), thirteen of them only during night-time. In conclusion, this study provides insight into the prevalence of respiratory symptoms in four genetic forms of CNM in the Netherlands and offers the basis for future natural history studies.</p

Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy

Amphiphysin 2, encoded by BIN1, is a key factor for membrane sensing and remodelling in different cell types. Homozygous BIN1 mutations in ubiquitously expressed exons are associated with autosomal recessive centronuclear myopathy (CNM), a mildly progressive muscle disorder typically showing abnormal nuclear centralization on biopsies. In addition, misregulation of BIN1 splicing partially accounts for the muscle defects in myotonic dystrophy (DM). However, the muscle-specific function of amphiphysin 2 and its pathogenicity in both muscle disorders are not well understood. In this study we identified and characterized the first mutation affecting the splicing of the muscle-specific BIN1 exon 11 in a consanguineous family with rapidly progressive and ultimately fatal centronuclear myopathy. In parallel, we discovered a mutation in the same BIN1 exon 11 acceptor splice site as the genetic cause of the canine Inherited Myopathy of Great Danes (IMGD). Analysis of RNA from patient muscle demonstrated complete skipping of exon 11 and BIN1 constructs without exon 11 were unable to promote membrane tubulation in differentiated myotubes. Comparative immunofluorescence and ultrastructural analyses of patient and canine biopsies revealed common structural defects, emphasizing the importance of amphiphysin 2 in membrane remodelling and maintenance of the skeletal muscle triad. Our data demonstrate that the alteration of the muscle-specific function of amphiphysin 2 is a common pathomechanism for centronuclear myopathy, myotonic dystrophy, and IMGD. The IMGD dog is the first faithful model for human BIN1-related CNM and represents a mammalian model available for preclinical trials of potential therapies