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Featured researches published by Hugh E. Vroman.


Journal of Insect Physiology | 1965

Effect of allatectomy on lipid biosynthesis and turnover in the female American cockroach, Periplaneta americana (L.)

Hugh E. Vroman; J.N. Kaplanis; W. E. Robbins

Abstract The control of the corpora allata over lipid biosynthesis and turnover was studied in the American cockroach, Periplaneta americana (L.), by using 1- 14 C-acetate as a precursor. The labelled acetate was injected into allatectomized and control roaches and the time-curve of the appearance of label in lipid fractions was determined. It was found that the greatest effect was in the triglyceride fraction, which was more than twice as much per roach in the operated insects, whereas no obvious effect was noted on the hydrocarbon fraction. Allatectomy noticeably slowed the turnover of both triglyceride and phospholipids.


Steroids | 1963

The absence of cholesterol biosynthesis in a primitive insect—the firebrat, thermobia domestica (packard)

J.N. Kaplanis; W. E. Robbins; Hugh E. Vroman; B.M. Bryce

Abstract It has been postulated that certain of the more primitive insects may be capable of residual cholesterogenesis in contrast to the higher forms in which this capacity was lost through evolution. The recent report of high incorporation of dietary 1−14C acetate into cholesterol by a silverfish merited examination in another primitive insect. Hence, several groups of firebrats, Thermobia domestica (Packard) were either fed on a diet containing 1−14C acetate or injected with an aqueous solution of the labeled compound. Radioanalysis of the total lipids indicated efficient incorporation of the 1−14C acetate for lipid synthesis by both routes of administration. Gas-liquid chromatographic analysis of the nonsaponifiable lipids revealed cholesterol to be the major sterol present. After the addition of purified carrier cholesterol, the sterols were isolated from the nonsaponifiable lipids by chroma-tography on alumina and digitonin precipitation. When the sterols from all the experiments were combined and purified through the dibromide, the cholesterol had a specific activity of 3.5 cpm/mg, yielding a total incorporation of about 39 cpm. This radioactivity represents about 0.001% of that incorporated into the total lipids. It is concluded that, because of the very low levels of radioactivity remaining in the cholesterol and the inability to obtain a constant specific activity throughout the purification process, there was no significant incorporation of 1−14C acetate into cholesterol by the firebrat.


Journal of Insect Physiology | 1967

The conversion of cholestanone to cholestanol by the housefly, Musca domestica L.

R.C. Dutky; W. E. Robbins; T.J. Shortino; J.N. Kaplanis; Hugh E. Vroman

Abstract Larvae of the housefly, Musca domestica L., reared aseptically on a semi-defined diet failed to develop when either cholestenone, cholestanone, or cholestanol was used as the sole source of dietary steroid. However, when these three steroids were tested for ‘sparing’ activity (in combination with a subminimal quantity of cholesterol) cholestanone and cholestanol were 66 and 79 per cent, respectively, as effective as an optimum concentration of cholesterol. Under the same conditions cholestenone showed only low biological activity (11 per cent). Biochemical studies with 4-14C-cholestanone indicate that the utilization of this steroid in the housefly larvae proceeds through its partial conversion to cholestanol. The identity of cholestanol as a metabolite of cholestanone was established by radiotracer techniques, gas-liquid chromatographic analysis, and by isolation of crystalline cholestanol from housefly pupae reared aseptically on a semi-defined diet containing cholestanone plus a subminimal amount of cholesterol. Using reverse isotope dilution techniques, no significant conversion of 14C-cholestanone to cholesterol was detected. In studies with adult insects, both males and females converted injected 14C-cholestanone to cholestanol.


Journal of Biological Chemistry | 1960

Studies of cholesterol biosynthesis. I. The identification of desmosterol in serum and tissues of animals and man treated with MER-29.

Joel Avigan; Daniel Steinberg; Hugh E. Vroman; Malcolm J. Thompson; Erich Mosettig


Biochemical and Biophysical Research Communications | 1963

Hydrocarbons of the American cockroach

Graeme L. Baker; Hugh E. Vroman; Joel Padmore


Journal of Lipid Research | 1967

Separation of sterol acetates by column and thin-layer argentation chromatography.

Hugh E. Vroman; Charles F. Cohen


Journal of Lipid Research | 1969

Synthesis of lipids from acetate by human preputial and abdominal skin in vitro

Hugh E. Vroman; R. A. Nemecek; S. L. Hsia


Journal of Chromatography A | 1965

LIMITS OF DETECTION OF SOME LIPIDS IN THIN-LAYER CHROMATOGRAPHY.

Hugh E. Vroman; Graeme L. Baker


Steroids | 1965

Deterioration of stored Δ24-sterols which contain a nuclear double bond

Malcolm J. Thompson; J.N. Kaplanis; Hugh E. Vroman


Journal of Lipid Research | 1963

EFFECT OF TRIPARANOL ON ATHEROSCLEROSIS AND ON STEROL COMPOSITION AND CONCENTRATION IN SERUM AND AORTA OF THE CHICKEN.

Harry Y. c. Wong; Joel Avigan; Robert L. Raiford; Ann Butler; Hugh E. Vroman

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J.N. Kaplanis

United States Department of Agriculture

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W. E. Robbins

United States Department of Agriculture

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Graeme L. Baker

United States Department of Agriculture

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Joel Avigan

National Institutes of Health

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Malcolm J. Thompson

National Institutes of Health

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B.M. Bryce

United States Department of Agriculture

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Erich Mosettig

National Institutes of Health

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Joel Padmore

United States Department of Agriculture

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