The solution of a dosimetry problem caused by a mercury shutter

Replies to L. E. Beutler et al (see record 1973-31675-001) who presented data in defense of using the number of patients rather than the number of therapists as the unit of analysis for assessing the reliability of process psychotherapy variables. The present paper presents data suggesting that the Beutler et al interpretation of their research findings is not valid. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Portal hypertension changes following selective splenorenal shunt surgery. Evaluation by percutaneous transhepatic portal catheterization, venography, and cinefluorography

A series of ergot alkaloids, together with the DA agonists apomorphine and piribedil, were tested for protective effects against audiogenic seizures in an inbred strain of mice (DBA/2) and for induction of circling behaviour in mice with unilateral destruction of one nigrostriatal DA pathway. The order of potency against audiogenic seizures was apomorphine greater than ergocornine greater than bromocryptine greater than ergometrine greater than LSD greater than methysergide greater than piribedil while that observed in the rotating mouse model was apomorphine greater than ergometrine greater than ergocornine greater than bromocryptine greater than piribedil. LSD caused only weak circling behaviour even when administered in high doses (greater than 1 mg/kg). Methysergide was ineffective. Prior administration of the neuroleptic agent haloperidol blocked the effect of DA agonists and of ergot alkaloids in both animal models. The possible action of ergot alkaloids as DA agonists is discussed.     

Rat mature sympathetic neurones derive neurotrophin 3 from peripheral effector tissues

In a previous study we have demonstrated that endogenous neurotrophin 3 (NT3) is required for the survival of most sympathetic neurones in postnatal rats. However, the mechanisms underlying the action of NT3 on sympathetic neurones is not known. Neither is it understood whether NT3 is retrogradely transported from peripheral tissues or acts locally in an autocrine fashion. In the present study, NT3-mRNA was quantified in sympathetic effector tissues and NT3 protein was localized in intact and lesioned sympathetic nerves in rats. NT3-mRNA is expressed and developmentally regulated in many effector tissues including mesenteric arteries, salivary gland, heart and kidney but hardly detectable in the superior cervical ganglia of adult animals. The majority of sympathetic neurones express immunoreactivity for TrkA and TrkC in both neonatal and adult rats. Sympathetic somata are normally immunoreactive for NT3, but the immunoreactivity is abolished by systemic administration of NT3 antibodies or axotomy of postganglionic neurones, suggesting an accumulation of NT3 from extraneuronal sources. Furthermore, the detection of NT3-immunoreactivity in the internal carotid nerve as early as 3 h following a compression and only on the distal side indicates endogenous NT3 is retrogradely transported by sympathetic neurones. These studies provide evidence indicating that NT3, like nerve growth factor, is an effector tissue-derived neurotrophic factor for sympathetic neurones both during development and in the adult animal. Thus, we have provided a clear example that one type of neurone derives, through a retrograde transport mechanism, two neurotrophic factors simultaneously from its peripheral effector tissues.     

Fate and efficiency of nitrogen fertilizers applied to wetland rice. II. Punjab,India

Two modified urea products (urea supergranules [USG] and sulfur-coated urea [SCU]) were compared with conventional urea and ammonium sulfate as sources of nitrogen (N), applied at 58 kg N ha^–1 and 116 kg N ha^–1, for lowland rice grown in an alkaline soil of low organic matter and light texture (Typic Ustipsamment) having a water percolation rate of 109 mm day^–1. The SCU and USG were applied at transplanting, and the whole dose of nitrogen was¹⁵N-labeled; the SCU was prepared in the laboratory and was not completely representative of commercial SCU. The SCU was broadcast and incorporated, whereas the USG was point-placed at a depth of 7–8 cm. The urea and ammonium sulfate applications were split: two-thirds was broadcast and incorporated at transplanting, and one-third was broadcast at panicle initiation. All fertilizers except the last one-third of the urea and ammonium sulfate were labeled with¹⁵N so that a fertilizer-N balance at flowering and maturity stages of the crop could be constructed and the magnitude of N loss assessed.At all harvests and N rates, rice recovered more¹⁵N from SCU than from the other sources. At maturity, the crop recovered 38 to 42% of the¹⁵N from SCU and only 23 to 31% of the¹⁵N from the conventional fertilizers, urea and ammonium sulfate, whose recovery rates were not significantly different. In contrast, less than 9% of the USG-N was utilized. Fertilizer nitrogen uptake was directly related to the yield response from the different sources. Most of the fertilizer N was taken up by the time the plants were flowering although recovery did increase up to maturity in some treatments.Analysis of the soil plus roots revealed that less than 1% of the added¹⁵N was in the mineral form. Between 20 and 30% of the¹⁵N applied as urea, SCU, and ammonium sulfate was recovered in the soil plus roots, mainly in the 0–15 cm soil layer. Only 16% of the¹⁵N applied as USG was recovered in the soil, and this¹⁵N was distributed throughout the soil profile to a depth of 70 cm, which was the lowest depth of sampling.Calculations of the¹⁵N balance showed that 46 to 50% of the urea and ammonium sulfate was unaccounted for and considered lost from the system. Only 27 to 38% of the¹⁵N applied as SCU was not recovered at maturity, but 78% of the USG application was unaccounted for. The extensive losses and poor plant recovery of USG at this site are discussed in relation to the high percolation rate, which is atypical of many ricegrowing areas.     

Developmental characteristics of histamine methyltransferase and phenylethanolamine-N-methyl-transferase of rat brain

The specific activity of histamine methyltransferase of rat brain increases rapidly from the 16th until the 25th day of gestation (7 days after birth). The specific activity of phenylethanolamine-N-methyl-transferase shows a rapid increase during the 1st and the 2nd week after birth, the adult values being obtained by the end of the 2nd week.