Follow-up and reasons for extended-release naltrexone discontinuation for alcohol use disorder after hospital initiation.

Only 1.9% of the individuals in the USA with alcohol use disorder (AUD) receive medication for AUD. Hospitalisation presents an opportunity to identify patients with AUD and offer treatment.

Extended-release naltrexone for people with alcohol use disorder on therapeutic anticoagulation: A case series.

What Is Known And Objective: Individuals with medication adherence challenges or a preference for long-acting medications may benefit from extended-release naltrexone (XR-NTX) for treatment of alcohol use disorder (AUD). Individuals on therapeutic anticoagulation were excluded from XR-NTX studies and its safety in this population has not been reported.

Case Summary: We conducted structured retrospective chart review of six individuals who received XR-NTX for AUD while on therapeutic anticoagulation between November 2019 and Deccember 2020.

Mechanochemistry of Cationic Cobaltocenium Mechanophore.

Recent research on the mechanochemistry of metallocene mechanophores has shed light on the force-responsiveness of these thermally and chemically stable organometallic compounds. In this work, we report a combination of experimental and computational studies on the mechanochemistry of main-chain cobaltocenium-containing polymers. Ester derivatives of the cationic cobaltocenium, though isoelectronic to neutral ferrocene, are unstable in the nonmechanical control experimental conditions that were accommodated by their ferrocene analogs.

Effect of SLCO1B1 T521C on Statin-Related Myotoxicity With Use of Lovastatin and Atorvastatin.

The association between the c.521T>C variant allele in SLCO1B1 (reference single nucleotide polymorphism (rs)4149056) and simvastatin-induced myotoxicity was discovered over a decade ago; however, whether this relationship represents a class effect is still not fully known. The aim of this study was to investigate the relationship between rs4149056 genotype and statin-induced myotoxicity in patients taking atorvastatin and lovastatin.

Influence of plating density on individual cell growth, cell division and differentiation of neonatal rat heart primary cultures.

The influence of plating cell density of an originally enriched myocardial cell population has been studied in neonatal rat heart cells in culture. Low density (LDM) is defined as a density (24 h after plating) of 209 +/- 44 cells/mm2 (mean +/- SEM) and is compared with high density (HDM), 419 +/- 67 cells/mm2. Cell growth is evaluated by the total cell number, the percentage of myocardial cells (M) in culture (PAS method) and the protein content per cell.

Effects of adriamycin on enzymes of adenine nucleotide metabolism in heart cell cultures.

Effects of adriamycin (ADM) treatment on rat heart cells in culture were examined. ADM treatment (lug/ml) for 3 hr, 48 to 51hr of culture age, had no effect on oxygen consumption, myosin content or myosin ATPase activity. In contrast, the activities of creatine kinase, adenylate kinase and adenosine deaminase were significantly lower in ADM-treated cells than in corresponding controls at 72 and 96 hr of culture age.

Oxygen consumption of mammalian myocardial cells in culture: measurements in beating cells attached to the substrate of the culture dish.

A Lucite attachment which permitted the measurement of oxygen consumption in cells in culture without manipulating the cells was constructed. The attachment fit over commercially available dishes for cell culture and had an oxygen electrode built into it. Oxygen uptake of cells in culture was thus measured.

Isozymes of creatine kinase in mammalian cell cultures.

Previous studies on the energy metabolism of rat myocardial cells in culture supported the hypothesis that the creatine-phosphocreatine-creatine kinase system plays an important role in the intracellular transport of energy from the mitochondria to the myofibrils and in the regulation of energy production coupled to energy utilization in this model system. Effective functional compartmentation of ATP could result from the binding of creatine kinase to cellular organelles (e.g.

Mitochondrial creatine kinase in mammalian myocardial cells in culture.

Previous studies on the energy metabolism of rat myocardial cells in culture supported the hypothesis that the creatine-phosphorylcreatine-creatine kinase system is essential for intracellular transport of energy from the mitochondria to the myofibrils and in the regulation of energy production to meet energy utilization. Effective functional compartmentation of ATP could result from the binding of creatine kinase to cellular organelles (e.g.

Metabolic involvement in adriamycin cardiotoxicity.

The cardiotoxic effects of adriamycin were studied in mammalian myocardial cells in culture as a model system. Adriamycin inhibited cell growth and the rhythmic contractions characteristic of myocardial cells in culture. A possible involvement of energy metabolism was suggested previously, and in this study the adenylate energy charge and phosphorylcreatine mole fraction were determined in the adriamycin-treated cells.

Replicative and unscheduled DNA synthesis in adriamycin-treated myocardial cells.

The effect of the potent antitumor antibiotic adriamycin (ADM) on chromosome integrity, DNA replication, and unscheduled DNA synthesis was investigated in cultured rat cardiac cells. Chromosome distribution, autoradiography, and [3H]thymidine (dThd) incorporation studies were carried out on separate cultures. A 3-hr pulse of ADM at a concentration of 1 microgram/ml was sufficient to cause chromosomal aberrations that were evident for up to 3 days post-ADM treatment.

Modification by adenosine of the effect of adriamycin on myocardial cells in culture.

The cardiotoxic effects of Adriamycin (ADM) were studied utilizing mammalian myocardial cells in culture as a model system. ADM inhibited cell growth and the rhythmic contractions characteristic of these cells. Because a possible involvement of energy metabolism in the action of ADM was suggested previously, the adenylate energy charge and phosphorylcreatine mol fraction were determined in the ADM-treated cells.

Differential effect of adriamycin on DNA replicative and repair synthesis in cultured neonatal rat cardiac cells.

The effect of the potent antitumor antiobiotic Adriamycin (ADM) on DNA replication and unscheduled DNA synthesis in cultured rat cardiac cells was investigated. Autoradiography and [3H]thymidine incorporation studies were carried out on parallel cultures. DNA replication was depressed for up to 6 days following a 3-hr pulse of ADM administration.

Cardiotoxic effects of adriamycin in mammalian cardiac cells in culture.

Cardiotoxicity of unknown etiology may preclude the use of adriamycin, a cancer chemotherapeutic agent. Mammalian cardiac cells in culture were used as a model system in the study of the mechanisms involved. Adriamycin inhibited cell growth, particularly of the fast-dividing nonmuscle cells.

Studies on the control of energy metabolism in mammalian cardiac muscle cells in culture.

Myocardial cells in a monolayer culture are a myogenic model system wihch shows functional differentiation and in which the intracellular metabolism and energy utilization do not differ markedly from those of the fresh tissue. In the myocardial cells, as in numerous other muscle tissues, the concentration of high energy phosphate compounds, primarily phosphorylcreatine, correlates well with the functional integrity of the cells. The decline of adenosine triphosphate (ATP) below a critical level leads to the cessation of rhythmic contractions of the cells in culture, and, conversely, an increased steady state level of ATP correlates with an increased rate of excitability.