Biomedical subjects
J Molin
Publications and source records attributed to J Molin.
Are pancreatic beta-cells under vagal control?
To elucidate the importance of cholinergic innervation for pancreatic beta-cells in vivo, atropine sulphate (0.2 mg/kg body weight) was subcutaneously injected into mice 4 times a day for 10 days. Control animals received 0.9% NaCl. Paraffin sections of the pancreas were stained for beta-cells with aldehyde fuchsin and for alpha-cells (glucagon cells) with silver according to Grimelius. Endocrine and exocrine cell nuclei were measured with an ocular screw micrometer. The light absorbance at 550 nm wave-length of aldehyde-fuchsin-stained islet sections was measured with a microscope photometer. Atropine caused no loss of body weight or apparent food consumption. The nuclei of beta-cells shrank significantly in response to atropine; A550 of islet surfaces showed a significant negative correlation to beta-cell nuclear size. Acinar cell nuclei near islets also became smaller after atropine treatment but to a lesser extent. No such change was observed in the alpha-cells. A trophic influence of the vagal nerve may be important for the long-term control of beta-cell function.
Roentgenologic appearance of fibromuscular dysplasia.
Clinical and roentgenologic findings in 100 hypertensive patients with fibromuscular disease of the renal arteries are presented and compared with the experiences obtained from previously reported large series. Frequency of bilateral disease and abnormal findings at urography, involvement of segmental arteries and occurrence of extrarenal manifestations are reported. A striking female preponderance is noted, and there is evidence that the disease inflicts middle-aged rather than young women.
Percutaneous nephropyelostomy in postrenal obstruction.
Explore the source record for details and available documents.
Experimental studies on the radiation-modifying effect of bleomycin in malignant and normal mouse tissue in vivo.
The interaction between bleomycin (BLM) and radiation was studied in a C3H mammary carcinoma and its surrounding normal skin. In the skin, single and fractionated doses of sequential treatment with BLM (25 mg/kg) 24 hours prior to radiation therapy did not influence the response to irradiation, whereas simultaneous treatment with BLM given 15 minutes before radiation therapy enhanced the reaction to irradiation by a factor of 1.2 or 1.4 following treatment with one fraction or five fractions, respectively. The tumor response to irradiation was not influenced by a single sequential treatment, but five daily fractions of radiation therapy following five daily dose fractions of BLM increased the radiation dose needed to control 50% of the tumors, probably because the tumors continued to grow during the BLM treatment. Simultaneous treatment enhanced the response to irradiation by a factor of 1.2 after both single-dose and fractionated therapy. Based on these data it was concluded that none of the combined treatment schedules were able to produce a better therapeutic effect than radiation therapy alone. Furthermore, mortality due to lung fibrosis in mice treated with BLM indicated the marked toxicity of the drug. This toxicity was most pronounced after fractionated treatment and when radiation therapy and BLM were given simultaneously.