Search NASA⌕ Search

SEARCH · Search NASA

Results for “IN VIVO”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1977

In-vivo bone strain telemetry in monkeys /M. nemestrina/

A new method for collecting in-vivo bone strain data in monkeys has been developed and tested. The method includes a system which consists of a new design of implantable strain transducer and its companion telemetry package. The transducer fits into a hole drilled in a monkey tibia and is threaded for subsequent bone ingrowth. The transducers and telemetry package are biocompatible for over 503 days. The telemetry package uses Pulse Interval Ratio Modulation (PIRM) to transmit strain information to receiving equipment located outside the animal housing cage.

Young, D. R.↗
NASA NTRS1979

Senescent changes in the ribosomes of animal cells in vivo and in vitro

The paper examines RNA-ribosomal changes observed in protozoa and fixed postmitotic cells, as well as the characteristics of intermitotic cells. Attention is given to a discussion of the implications of the reported ribosomal changes as to the senescent deterioration of protein synthesis and physiological functions. A survey of the literature suggests that, while the data on ribosomal change in dividing cells both in vivo and in vitro are inconclusive, there is strong histological and biochemical evidence in favor of some degree of quantitative ribosomal loss in fixed postmitotic cells. Since these decreases in ribosomes are demonstrated in differential cells from nematodes, insects and mammals, they may represent a universal manifestation of cytoplasmic senescence in certain types of fixed postmitotic animal cells. The observed variability in ribosomal loss for cells belonging to the same type suggests that this involution phenomenon is rather related to the wear and tear suffered by a particular cell.

Miquel, J.↗
NASA NTRS1979

Estimation of the depth of sunlight penetration in natural waters for the remote sensing of chlorophyll a via in vivo fluorescence

In attempting to measure remotely the constituents of the ocean through spectral analysis of diffusely reflected sunlight, it is important to know the depth over which constituent concentrations can be estimated. Recently, considerable interest has been generated in the use of sunlight-excited fluorescence of chlorophyll a contained in photoplankton (in vivo) to determine remotely the chlorophyll a concentration in surface waters. In the present paper an estimate is provided for the depth to which chlorophyll a concentration can be determined from observations of the fluorescence.

Gordon, H. R.↗
NASA NTRS1983

Androgens enhance in vivo 2-deoxyglucose uptake by rat striated muscle

It is shown that testosterone propionate (TP) causes a striking increase in the in vivo uptake of 2-deoxyglucose (2-DG) by the levator ani muscle of immature male rats, which was found to be uniformly distributed over the entire muscle. After a single subcutaneous injection of TP, no enhancement of 2-DG was observed before 3.5 hr, at which time uptake was increased 2-fold; maximum enhancement (4-fold) was attained at 12 hr. At 72 hr, 2-DG uptake remained elevated at twice the control value. It was determined that the effect of TP probably is mediated by specific androgen receptors. In addition, it was found that the effect of TP was blocked by the simultaneous administration of an androgen antagonist, cyproterone acetate. TP also was found to enhance the uptake of 2-DG in the bulbocavernosus (253 percent over control) and extensor digitorum longus muscles (150 percent over control), but not in the biceps brachii or soleus. It is suggested that the increased uptake of glucose may be an important early step in the anabolic response of muscle to androgens.

Max, S. R.↗
NASA NTRS1984

Growth and differentiation of mammalian embryonic tissues exposed to hypergravity in vivo and in vitro

In about 10 years or so, men and women from Earth will be long-term inhabitants of a space station aboard which plants and animals will be growing and developing in gravities other than that of Earth. The effect of gravitational changes on development was examined. It is indicated that differentiation is speeded up under excess G and slowed in low or null G. The effects of exposure to excess gravity on fusion of the embryonic mouse secondary palate were studied. During fusion, the palatal shelves first adhere by means of glycoproteins appearing along the medial epithelial edge (MEE). The contacting epithelia then reorganize and undergo programmed cell death, allowing the underlying mesenchymes to come in contact. The process of cell death occurs in vitro at about the same rate that it occurs in vivo.

Duke, P. J.↗
NASA NTRS1984

Interferon induces natural killer cell blastogenesis in vivo

Interferon (IFN), types beta and gamma, and IFN inducers polyinosinic-polycytidylic acid and lymphocytic choriomeningitis virus, all stimulated the generation of blast-natural killer (NK) cells in mouse spleens, Blast-NK cells were characterized on the basis of size, 3H-thymidine uptake, and NK cell markers These data indicate that in addition to augmenting NK cell-mediated lysis, IFN may regulate NK cell proliferation in vivo.

Biron, C. A.↗
NASA NTRS1985

Growth and differentiation of mammalian embryonic tissues exposed to hypergravity in vivo and in vitro

Decreased cartilage areas in embryonic limbs developing under excess g in vitro, is reported, as well as delayed skeletal development in embryos and fetuses exposed to excess g in utero. 12.5-day mouse limb buds were cultured at 2.6 g, and fixed at two days and six days of culture. In vivo experiments used alizarin-stained 18-day fetuses exposed to 2.3 g. In all studies, cartilage areas were determined using a digitized tablet. Form factor analysis determined that the main effect of in vitro centrifugation was a reduction in length of the limb elements, probably due to the precocious chondrogenesis seen in the upper regions of centrifuged limbs. Similar reductions in length of ossified areas was seen in the in utero studies.

Duke, J.↗
NASA NTRS1992

In Vivo and in Vitro Chlorophyll-a and Pheophytin-a Concentration Measurements by Laser Fluorometry

Discussed here is the application of a laser fluorescent technique in in vivo and in vitro phyto- and zooplankton analysis involving popular lasers, an impulse YAG laser (lambda = 532 nm) and a steady state He-Cd (lambda = 440 nm). The YAG laser is widely used in laser remote sensing of seawater photoplankton in situ mode, but here we give special attention to its use in the precise estimation of phytoplankton pigments using laser induced fluorescence. The He-Cd laser is a novice in this field and, we believe, very promising. Our methods enable one to detect, in viro, chlorophyll-a (Chl-a) concentration in the water probe up to 10 nanograms per liter, and to measure, in vitro, Chl-a and pheophytin-a (Ph-a) concentrations in acetone extracts of phyto- and zooplankton up to 1 nanogram per liter.

Demidov, A. A.↗
NASA NTRS1992

In vivo testing confirms a blunting of the human cell-mediated immune mechanism during space flight

The cell-mediated immune (CMI) mechanism was evaluated in 10 space shuttle astronauts by measuring their delayed-type hypersensitivity response to seven common recall antigens. The Multitest CMI test system was used to administer antigens of tetanus, diphtheria, Streptococcus, Proteus, old tuberculin, Candida, and Trichophyton to the forearm 46 h before nominal mission termination; readings were conducted 2 h after landing. The mean number of reactions was reduced from 4.5 preflight to 3.0 inflight, and the mean reaction score was reduced from 21.4 to 13.7 mm inflight. The data presented suggest that the CMI system is still being degraded by space flight conditions on day 4 and that between day 5 and day 10, the depression maximizes and the system begins to adjust to the new conditions. The relation of these in vivo findings to previously reported in vitro results is discussed.

Taylor, G. R.↗