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Biomedical subjects

B J Morris

Publications and source records attributed to B J Morris.

At least 181 records · Page 10Linked to original sources

Activation by puff adder venom of inactive renin in normal and hypertensive rat plasma.

Inactive renin has been studied extensively in human plasma, but in animal plasma its accurate quantification has proved more difficult, due partly to higher activity of plasma protease inhibitors. Such activity in human plasma can be conveniently destroyed by a metalloprotease in Bitis arietans venom, with concommitant release of endogenous enzyme activities, such as plasma kallikrein, that then activate inactive renin. It was therefore of interest to look for inactive renin in rat and rabbit plasma using this approach, so providing, in addition, a comparison for the disparate data of other groups who have used trypsin or acid for activation. In both rat and rabbit plasma the proportion of inactive renin was 62% of total renin, whereas human plasma contained more inactive renin and a higher proportion, 82%. A higher concentration of venom was required for rat (33 ug venom/ml plasma) and rabbit (4 micrograms/ml) than needed for activation, at a similar rate, in human plasma (1 microgram/ml). When applied to studies of rats made hypertensive and hyper-reninaemic by aortic ligation for 5 days, higher total (active + inactive) renin was observed. The proportion of inactive renin, as a percentage of total renin in plasma collected at this time, was, however, found to diminish significantly. In conclusion, puff adder venom activates inactive renin in rat and rabbit plasma and can be used to study physiological changes in inactive renin in such animal plasma.

Animals↗

Regional chromosomal assignment of human renin gene to 1q12----qter and use in linkage studies in Charcot-Marie-Tooth disease.

The gene for renin, previously mapped to human chromosome 1, was further localized to 1q12----qter using human-mouse somatic cell hybrid DNAs. The renin DNA probe used (lambda HR5) could detect a HindIII restriction fragment length polymorphism. When used in studies of 12 informative families, no linkage could be found between the renin gene and Charcot-Marie-Tooth disease. Furthermore, an association of any renin allele with hypertension was not apparent.

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Autoradiographic distribution in rat brain of a non-conventional binding site for the opiate [3H]diprenorphine.

[3H]Diprenorphine, in the presence of saturating concentrations of mu, delta and kappa opiate receptor blocking agents, was found to label an additional binding site in rat brain, for which various opiates showed moderate affinity. Using light microscopic autoradiography, a unique, highly discrete distribution of binding sites was found, with a high density only in the globus pallidus, substantia nigra, interpeduncular nucleus, parabrachial nuclei and locus coeruleus. The identity of this binding site remains unclear.

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Localization of prodynorphin messenger rna in rat brain by in situ hybridization using a synthetic oligonucleotide probe.

An in situ hybridization technique has been developed to study the distribution of messenger RNA (mRNA) encoding prodynorphin (proenkephalin B) in sections of rat brain. A 100-mer oligonucleotide was used as a template to synthesize a 32P-labelled DNA probe complementary to the coding region of rat prodynorphin mRNA. Using this probe, dense labelling was observed in the supraoptic and paraventricular nuclei of the hypothalamus, in the striatum and in the dentate gyrus. The results show for the first time the localization of prodynorphin mRNA in rat brain, and additionally demonstrate the usefulness of oligonucleotides to detect rare mRNAs by in situ hybridization.

Animals↗

Autoradiographic localization in rat brain of kappa opiate binding sites labelled by [3H]bremazocine.

[3H]Bremazocine, in the presence of saturating concentrations of mu and delta receptor blocking agents, was used to label putative kappa opiate binding sites in rat brain. The binding of [3H]bremazocine under these conditions was completely displaced with high affinity by U-50488H and dynorphin1-17, and the potency of a series of opiate ligands was consistent with an action at kappa receptors. Therefore, [3H]bremazocine, in the presence of mu and delta blockers, was used to localize U-50488H-displaceable kappa binding sites by autoradiography. A distribution different from that of mu and delta receptors was seen, with levels highest in the claustrum, striatum, medial preoptic area, suprachiasmatic nucleus, medial amygdala and superior layer of the superior colliculus. The results show that the U-50488H-displaceable kappa sites have a distinct distribution which is discussed in terms of the possible functional roles of kappa receptors.

3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cycloh↗

Evolution of renin.

New gene data for three aspartyl proteases (human renin, mouse renin and human pepsin) permitted closer analysis of the gene duplication and fusion hypothesis for the evolution of this family of enzymes. Alignment of sequences in the hemilobes of human pepsin revealed only weak homology in amino acid sequences. Nucleotides were, however, more homologous. Splice junctions between putative duplicated exons did not match. Repeated sequences in the human renin gene were detected by hybridization with total human DNA labelled with 32P. These were not, however, consistent with unequal crossing-over between repeated sequences of an ancestral gene having occurred. The data thus provide no immediate support for the gene duplication and fusion hypothesis. The symmetry in structure of an aspartyl protease may arise from the tendency of hydrophilic amino acids to be encoded at splice junctions. This would divide a molecule comprised mainly of beta-sheets into roughly superimposable domains.

Animals↗

Stimulation by thyroid hormone of renin mRNA in mouse submandibular gland.

Renin in the female mouse submandibular gland (SMG) is known to increase in response to thyroid hormone. In the present study a 500 base-pair renin cDNA was used to quantify renin mRNA, the product of transcription of the Ren-2 gene, in the female mouse SMG in response to thyroid hormone to assess more directly the nature of stimulation of renin biosynthesis. After daily injection for 1 wk renin mRNA increased from control values of 36 +/- 3 SE ng/g tissue to 212 +/- 41 with triiodothyronine (T3; P less than 0.005) and to 217 +/- 33 with thyroxine (T4; P less than 0.005). Treatment of mice with propylthiouracil (PTU) decreased renin mRNA to 1.2 +/- 0.3 (P less than 0.005) and after subsequent injection of T3 for 1 wk renin mRNA increased to 289 +/- 35 ng/g tissue. The time course of the response to a single injection of thyroid hormone indicated a rapid response with significant increases in renin mRNA by 1 h, reaching values 3.5 +/- 0.4 times control (P less than 0.005) by 5 h. Such rapid effects are consistent with a direct nuclear action of thyroid hormone in stimulating transcription of the Ren-2 gene in mouse submandibular gland or in stabilization of nuclear precursor renin mRNA or both.

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Human cardiac myosin heavy chain genes. Isolation of a genomic DNA clone and its characterization and of a second unique clone also present in the human genome.

A gene sequence coding for myosin heavy chain (MHC) of human cardiac muscle was isolated by screening a human genomic library with a 32P-labelled 1.1kb SacI restriction fragment from a previously characterized cDNA clone specifying the light meromyosin and 3' untranslated region of mRNA encoding rabbit cardiac alpha-MHC. The DNA of this human genomic clone (lambda HCMHC8) hybridized much more strongly than did other clones isolated under similar, low stringency conditions both to the rabbit cDNA probe and to mRNA isolated from rat cardiac, but not skeletal, muscle tissue. Probe made from a DNA restriction fragment of lambda HCMHC8 hybridized a single 31S band of human ventricular mRNA. This size is identical to that of cardiac MHC mRNA of other species. Heteroduplex analysis showed hybridization of lambda HCMHC8 with exon segments in a rabbit cardiac MHC genomic clone (lambda MHC alpha 12/1). It also showed that lambda HCMHC8 spanned 14 kb of DNA and contained exon segments estimated to code for two-thirds of a MHC including the carboxylic acid terminus. By rescreening the library under more stringent conditions, where only DNA sequences having strong homology to cardiac MHC genes would be expected to hybridize, clones having restriction maps overlapping lambda HCMHC8 were isolated together with a unique clone (lambda HCMHC9). DNA gel blot hybridization of human genomic DNA with lambda HCMHC8 probe at medium stringency gave a pattern of restriction fragments similar to the restriction map of lambda HCMHC8. A weaker set of bands also appeared which corresponded in pattern to the map of lambda HCMHC9.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Antihypertensive effect of sialoadenectomy in one-kidney, one clip hypertension in the rat.

We have examined the effect of removal of the submandibular gland on one-kidney, one clip (1K1C) hypertension in the rat. Five weeks after application of a silver clip with a 0.20-mm gap, 15 hypertensive rats were sialoadenectomized. This was followed by a decrease in systolic blood pressure (SBP) within 1 day by 22 +/- 4 mmHg (+/- s.e.m.) and in nine rats pressure stabilized within 1 week at 133 +/- 5 (cf. 166 +/- 2 before sialoadenectomy). In the other six rats the initial hypotensive response was followed by a gradual return to hypertensive levels, reaching 178 +/- 4 mmHg 6 weeks later. Sham-sialoadenectomized rats remained hypertensive throughout. When a 0.15-mm gap clip was used in a similar experiment rats became hypertensive after 2 weeks, and sialoadenectomy lowered SBP to normal in half of them, after which pressure tended to return to hypertensive levels in most. No change in SBP was found in sham-operated hypertensive rats. Sialoadenectomy performed at the time of clipping with a 0.15-mm gap clip and unilateral nephrectomy delayed the development of hypertension. Systolic pressure then fell from 153 +/- 14 at 4 weeks to 105 +/- 8 at 12 weeks after operation in five rats, but continued to increase in eight rats from 148 +/- 10 at 4 weeks to 172 +/- 15 at 12 weeks. These experiments thus demonstrate that the submandibular gland may contribute to the onset and maintenance of one-kidney, one clip hypertension in the rat, particularly in less severe stenosis.

Adrenal Cortex↗

Studies of the regulation of mouse renin genes by measurement of renin messenger ribonucleic acid.

The transcriptional activity of renin genes in the mouse kidney and submandibular gland (SMG) was examined by measurement of renin messenger RNA (mRNA) (nanograms per g tissue) and compared with renin activity (micromoles angiotensin I per h/g tissue). In control adult mice renin mRNA and renin activity (in parentheses) were 1.8 +/- 0.24 (11 +/- 1.1) in male kidney, 3.6 +/- 0.66 (18 +/- 2.8) in female kidney, 230 +/- 34 (903 +/- 59) in male SMG, and 31 +/- 6 (188 +/- 47) in female SMG (mean +/- SE, n = 6). The ratio of renin mRNA among these four tissues was similar to that of renin activity (1:2:100:17, respectively). Although the values in male kidney were one one-hundredth those in SMG, 1000 to 10000 times more SMG cells are involved per gram of tissue so that, per renin-synthesizing cell, kidney values would be 10 to 100 times SMG values. Expression of renin gene(s) in a renal juxtaglomerular cell may thus be higher than in a SMG granular duct cell. Values in adult male SMG were a consequence of a 40-fold rise at puberty, were decreased to 16% (+/- 3.8) by castration, but were not significantly influenced by treatment with testosterone, T4, propylthiouracil, sodium depletion, or spironolactone. Renin mRNA in adult female SMG was 18-fold higher than juvenile values, was increased 10-fold (+/- 1.6) by testosterone (to adult male levels) and 5.5-fold (+/- 0.81) by T4 (P less than 0.005), but was decreased to 42% (+/- 29) of normal by propylthiouracil (P less than 0.05). Propylthiouracil caused a small but significant decrease in testosterone-treated female values. In the kidney renin mRNA was increased 3.0-fold (+/- 0.30) by captopril, 2.3-fold (+/- 0.23) by a low sodium diet, and 1.7-fold (+/- 0.13) by spironolactone after 1 week, whereas T4, testosterone, or propylthiouracil had little or no effect. Sialoadenectomy increased renin mRNA and renin in male but not in female kidney, suggesting that a SMG factor, possibly renin, may have a role in suppression of renin synthesis in male kidney. In conclusion, measurement of renin mRNA suggests that testosterone regulates renin gene expression by a direct effect in male mouse SMG, whereas in the female regulation is by thyroid hormone. In the kidney conditions which increase renin content are accompanied by parallel (5-fold higher) increases in renin mRNA, suggesting enhanced expression of renin gene(s) in renal juxtaglomerular cells in chronic low sodium states.

Animals↗

Primary structure of the human renin gene.

The gene encoding human renin has been isolated on two overlapping clones from a bacteriophage lambda library of human DNA. The entire gene spans about 12,000 bp and contains 10 exons separated by 9 intervening sequences. The gene structure is similar to that of human pepsinogen in terms of overall size, homology in the coding regions, position of introns, and sizes of the exons, suggesting that the two genes are evolutionarily related. However, a novel exon coding for only three amino acids was detected that is not present in the pepsinogen gene and whose amino acids are also not found in mouse renin. Although the nucleotide sequence of the 5'-flanking DNA differs from that of the pepsinogen gene, in both cases this region contains a structure of almost perfect dyad symmetry which immediately precedes the TATA box and may have functional importance. Furthermore, sequences resembling the putative consensus sequence for glucocorticoid regulation of gene expression are located approximately 200 and 300 bp upstream from the gene. The overall structural anatomy suggests that the human renin gene evolved by mechanisms that include a duplication of exon segments, particularly those containing the codons for the catalytically important aspartate residues, together with the insertion of other exon and flanking DNA structures. An analysis of human chromosomal DNA demonstrates that there is only one gene with high homology to human renin.

Base Sequence↗

Human renin gene sequence, gene regulation and prorenin processing.

Human DNA coding for renin was identified and sequenced. The gene consisted of 10 exons corresponding to a 1500 nucleotide mRNA was broken up by long stretches of 'nonsense' DNA (introns) and spanned 12,000 base pairs. In addition, the sequence of nucleotides involved in regulation of the gene was determined by sequencing upstream. Prediction of the amino acid sequence of human preprorenin revealed likely sites of processing. This helps explain many past experimental observations. For example, the pro region contained adjacent likely cleavage sites for trypsin and pepsin and so reveals why both trypsin and pepsin can activate prorenin. The structure of human renin had features involved in its highly specific hydrolysis of the Leu10-Val11 bond unique to human angiotensinogen: in particular leucine 224 (instead of valine). Renin gene expression was studied in the mouse by quantification of both renin activity and its mRNA. Sodium depletion, captopril and spironolactone increased expression of Ren-1 in the kidney. The unusual, duplicated, mouse gene, Ren-2, which is expressed in the submandibular gland was, regulated by (dihydro)testosterone in male mice and by thyroid hormone in female mice.

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The biosynthetic pathway of renin in mouse submandibular gland.

The present study set out to demonstrate the biosynthesis of a prorenin and its processing in the cell, using the richest known natural source of renin, the mouse submandibular gland. Cell-free translation of total poly(A+) RNA or mRNA selected using a renin cDNA yielded Mr = 45,000 preprorenin which in the presence of dog pancreatic microsomal membranes, was converted to Mr = 43,000 prorenin. The latter was seen during in vitro labeling of tissue with [35S]methionine. Prorenin was synthesized first and converted rapidly to Mr = 38,000 single chain renin. Renin was then hydrolyzed slowly to give two chains of Mr = 33,000 and 5,000 held together by disulfide bonds. The Mr = 38,000 and 33,000 species had similar peptide maps. Western blotting of fractions from a pepstatin affinity column identified the separation of prorenin from renin. The results suggested that both single and two-chain renin have an exposed active site. Testosterone stimulated synthesis of prorenin during in vitro labeling of female tissue. Thus, mouse renin is synthesized as a preprorenin (Mr = 45,000) which is converted to a prorenin (Mr = 43,000) and then to renin (Mr = 38,000) by rapid processing within the cell, after which renin is cut slowly to give a two-chain form.

Animals↗

Immunohistochemistry of tonin in rat submandibular gland during development, lactation and secretion.

Tonin is a serine protease found in high concentrations in the submandibular gland (SMG) of the adult rat where it has been localized by immunohistochemistry in the granular ducts. The present study examined the development of tonin in the SMG, the effect of lactation and of stimulation of tonin release, using the peroxidase-antiperoxidase technique and antitonin. Tonin-like immunoreactivity first appeared in the primitive striated duct of the SMG on day 19 foetal and increased in intensity as the ducts developed into granular ducts. Reaction product in granules was seen on day 17 postpartum. Its localization within granules was established by immunochemistry of Sepharose beads to which had been coupled the contents of granules isolated from adult rats. The granular ducts of female rats, which are less developed than in the male, showed a marked increase in tonin-immunoreactivity during lactation. Stimulation of tonin secretion by isoprenaline caused massive discharge of tonin-like immunoreactivity into the lumen of the granular ducts during in vitro incubation. However, within one hour complete regranulation was apparent. The secretion was prevented by propranolol. The results indicate that tonin or a tonin-like substance appears in the rat submandibular gland late in gestation in ducts that presumably develop into granular ducts where it is found in abundance in granules in the adult, that the amount in females is increased during lactation, and that most of the granules are discharged during stimulation, only to be rapidly replaced.

Animals↗

Plasma vasopressin in hypercalcaemic states.

Plasma vasopressin was measured by radioimmunoassay in eight normal subjects and in six patients with hypercalcaemia. Vasopressin levels were significantly elevated in the hypercalcaemic patients, although urine osmolalities were lower than in controls. This finding is consistent with a renal resistance to the action of endogenous vasopressin in hypercalcaemia.

Adult↗

Detection of renin mRNA in mouse kidney and submandibular gland by hybridization with renin cDNA.

The presence of renin mRNA in a tissue is a manifestation of the expression of the renin gene by that tissue. In the present study 32P-labeled, single-stranded renin complementary DNA was used as a specific probe for the detection of renin mRNA in tissues by hybridization of their complementary base sequences. With use of the technique of hybridization histochemistry, renin cDNA probe bound strongly to sections of submandibular gland from male Quackenbush mice, a tissue which displays high androgen-dependent renin synthesis. Less was present in the female gland. In the kidney the probe localized in the cortex. A dot hybridization assay was developed to measure renin mRNA in serially diluted total RNA spotted onto nitrocellulose filters along with renin cDNA standards. From the concentration the ratio of renin mRNA between male and female submandibular gland and kidney was calculated as approx. 100:8:1:1, respectively, which is similar to the relative proportion of renin concentrations between these tissues. The present study thus provides the basis for investigations of the expression of the renin gene by tissues, particularly those with high renin biosynthetic activity.

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